Canonical Allele Identifier: CA1673238116

Gene: SYNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152239820_152239821delinsAG , CM000668.2:g.152239820_152239821delinsAG	GRCh38
NC_000006.11:g.152560955_152560956delinsAG , CM000668.1:g.152560955_152560956delinsAG	GRCh37
NC_000006.10:g.152602648_152602649delinsAG	NCBI36
NG_012855.1:g.402579_402580delinsCT
NG_012855.2:g.402579_402580delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.19894-115_19894-114delinsCT MANE Select	ENSP00000356224.5:n.19894-115_19894-114delinsCT
ENST00000423061.6:c.19681-115_19681-114delinsCT	ENSP00000396024.1:n.19681-115_19681-114delinsCT
ENST00000341594.9:c.18679-115_18679-114delinsCT	ENSP00000341887.6:n.18679-115_18679-114delinsCT
ENST00000367255.9:c.19894-115_19894-114delinsCT	ENSP00000356224.5:n.19894-115_19894-114delinsCT
ENST00000367256.9:n.3586-115_3586-114delinsCT
ENST00000409694.6:n.3478-115_3478-114delinsCT
ENST00000423061.5:c.19681-115_19681-114delinsCT	ENSP00000396024.1:n.19681-115_19681-114delinsCT
NM_033071.3:c.19681-115_19681-114delinsCT	NP_149062.1:n.19681-115_19681-114delinsCT
NM_182961.3:c.19894-115_19894-114delinsCT	NP_892006.3:n.19894-115_19894-114delinsCT
XM_006715407.1:c.19930-115_19930-114delinsCT	XP_006715470.1:n.19930-115_19930-114delinsCT
XM_006715408.1:c.19918-115_19918-114delinsCT	XP_006715471.1:n.19918-115_19918-114delinsCT
XM_006715409.1:c.19909-115_19909-114delinsCT	XP_006715472.1:n.19909-115_19909-114delinsCT
XM_006715410.1:c.19930-115_19930-114delinsCT	XP_006715473.1:n.19930-115_19930-114delinsCT
XM_006715411.1:c.19879-115_19879-114delinsCT	XP_006715474.1:n.19879-115_19879-114delinsCT
XM_006715412.1:c.19915-115_19915-114delinsCT	XP_006715475.1:n.19915-115_19915-114delinsCT
XM_006715413.1:c.19930-115_19930-114delinsCT	XP_006715476.1:n.19930-115_19930-114delinsCT
XM_006715414.1:c.19858-115_19858-114delinsCT	XP_006715477.1:n.19858-115_19858-114delinsCT
XM_006715415.1:c.19930-115_19930-114delinsCT	XP_006715478.1:n.19930-115_19930-114delinsCT
XM_006715416.1:c.19915-115_19915-114delinsCT	XP_006715479.1:n.19915-115_19915-114delinsCT
XM_006715417.1:c.19789-115_19789-114delinsCT	XP_006715480.1:n.19789-115_19789-114delinsCT
XM_006715420.1:c.19777-115_19777-114delinsCT	XP_006715483.1:n.19777-115_19777-114delinsCT
XM_006715421.1:c.19774-115_19774-114delinsCT	XP_006715484.1:n.19774-115_19774-114delinsCT
XM_006715422.1:c.19771-115_19771-114delinsCT	XP_006715485.1:n.19771-115_19771-114delinsCT
XM_006715423.1:c.19930-115_19930-114delinsCT	XP_006715486.1:n.19930-115_19930-114delinsCT
XM_006715424.1:c.19930-115_19930-114delinsCT	XP_006715487.1:n.19930-115_19930-114delinsCT
XM_006715425.1:c.19930-115_19930-114delinsCT	XP_006715488.1:n.19930-115_19930-114delinsCT
XM_011535641.1:c.19927-115_19927-114delinsCT	XP_011533943.1:n.19927-115_19927-114delinsCT
XM_011535642.1:c.19915-115_19915-114delinsCT	XP_011533944.1:n.19915-115_19915-114delinsCT
XM_011535643.1:c.19765-115_19765-114delinsCT	XP_011533945.1:n.19765-115_19765-114delinsCT
XM_011535644.1:c.18205-115_18205-114delinsCT	XP_011533946.1:n.18205-115_18205-114delinsCT
XM_011535645.1:c.17698-115_17698-114delinsCT	XP_011533947.1:n.17698-115_17698-114delinsCT
XM_011535647.1:c.13165-115_13165-114delinsCT	XP_011533949.1:n.13165-115_13165-114delinsCT
XM_006715408.2:c.19918-115_19918-114delinsCT	XP_006715471.1:n.19918-115_19918-114delinsCT
XM_006715410.2:c.19930-115_19930-114delinsCT	XP_006715473.1:n.19930-115_19930-114delinsCT
XM_006715412.2:c.19915-115_19915-114delinsCT	XP_006715475.1:n.19915-115_19915-114delinsCT
XM_006715413.2:c.19930-115_19930-114delinsCT	XP_006715476.1:n.19930-115_19930-114delinsCT
XM_006715415.2:c.19930-115_19930-114delinsCT	XP_006715478.1:n.19930-115_19930-114delinsCT
XM_006715416.2:c.19915-115_19915-114delinsCT	XP_006715479.1:n.19915-115_19915-114delinsCT
XM_006715417.2:c.19789-115_19789-114delinsCT	XP_006715480.1:n.19789-115_19789-114delinsCT
XM_006715420.2:c.19777-115_19777-114delinsCT	XP_006715483.1:n.19777-115_19777-114delinsCT
XM_006715421.2:c.19774-115_19774-114delinsCT	XP_006715484.1:n.19774-115_19774-114delinsCT
XM_006715423.2:c.19930-115_19930-114delinsCT	XP_006715486.1:n.19930-115_19930-114delinsCT
XM_006715424.2:c.19930-115_19930-114delinsCT	XP_006715487.1:n.19930-115_19930-114delinsCT
XM_006715425.2:c.19930-115_19930-114delinsCT	XP_006715488.1:n.19930-115_19930-114delinsCT
XM_011535641.2:c.19927-115_19927-114delinsCT	XP_011533943.1:n.19927-115_19927-114delinsCT
XM_011535642.2:c.19915-115_19915-114delinsCT	XP_011533944.1:n.19915-115_19915-114delinsCT
XM_011535645.2:c.17698-115_17698-114delinsCT	XP_011533947.1:n.17698-115_17698-114delinsCT
XM_017010608.1:c.19930-115_19930-114delinsCT	XP_016866097.1:n.19930-115_19930-114delinsCT
XM_017010609.1:c.19930-115_19930-114delinsCT	XP_016866098.1:n.19930-115_19930-114delinsCT
XM_017010610.1:c.19909-115_19909-114delinsCT	XP_016866099.1:n.19909-115_19909-114delinsCT
XM_017010611.2:c.19903-115_19903-114delinsCT	XP_016866100.1:n.19903-115_19903-114delinsCT
XM_017010612.1:c.19852-115_19852-114delinsCT	XP_016866101.1:n.19852-115_19852-114delinsCT
XM_017010613.1:c.19927-115_19927-114delinsCT	XP_016866102.1:n.19927-115_19927-114delinsCT
XM_017010614.1:c.19774-115_19774-114delinsCT	XP_016866103.1:n.19774-115_19774-114delinsCT
XM_017010615.1:c.19774-115_19774-114delinsCT	XP_016866104.1:n.19774-115_19774-114delinsCT
XM_017010616.1:c.19930-115_19930-114delinsCT	XP_016866105.1:n.19930-115_19930-114delinsCT
XM_017010617.1:c.19927-115_19927-114delinsCT	XP_016866106.1:n.19927-115_19927-114delinsCT
XM_017010618.1:c.19915-115_19915-114delinsCT	XP_016866107.1:n.19915-115_19915-114delinsCT
XM_017010619.1:c.18205-115_18205-114delinsCT	XP_016866108.1:n.18205-115_18205-114delinsCT
XR_001743287.1:n.20448-115_20448-114delinsCT
NM_182961.4:c.19894-115_19894-114delinsCT MANE Select	NP_892006.3:n.19894-115_19894-114delinsCT
NM_033071.5:c.19681-115_19681-114delinsCT	NP_149062.2:n.19681-115_19681-114delinsCT