Canonical Allele Identifier: CA366080480
Gene: SYNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152140073A>T , CM000668.2:g.152140073A>T GRCh38
NC_000006.11:g.152461208A>T , CM000668.1:g.152461208A>T GRCh37
NC_000006.10:g.152502901A>T NCBI36
NG_012855.1:g.502327T>A
NG_012855.2:g.502327T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.1869T>A MANE Plus Clinical ENSP00000346701.4:p.Phe623Leu
ENST00000367255.10:c.25335T>A MANE Select ENSP00000356224.5:p.Phe8445Leu
ENST00000423061.6:c.25191T>A ENSP00000396024.1:p.Phe8397Leu
ENST00000672154.1:c.737T>A
ENST00000672169.1:c.1070T>A
ENST00000673173.1:c.979T>A
ENST00000673451.1:c.1107T>A ENSP00000500189.1:p.Phe369Leu
ENST00000341594.9:c.24120T>A ENSP00000341887.6:p.Phe8040Leu
ENST00000347037.9:n.2083T>A
ENST00000354674.4:c.1869T>A ENSP00000346701.4:p.Phe623Leu
ENST00000367251.7:c.4170T>A ENSP00000356220.3:p.Phe1390Leu
ENST00000367255.9:c.25335T>A ENSP00000356224.5:p.Phe8445Leu
ENST00000367256.9:n.9027T>A
ENST00000367257.8:c.3273T>A ENSP00000356226.4:p.Phe1091Leu
ENST00000409694.6:n.8919T>A
ENST00000423061.5:c.25191T>A ENSP00000396024.1:p.Phe8397Leu
ENST00000460912.6:n.1949T>A
ENST00000478916.5:n.4357T>A
ENST00000536990.5:n.2172T>A
ENST00000539504.5:c.1800T>A ENSP00000441052.1:p.Phe600Leu
NM_033071.3:c.25191T>A NP_149062.1:p.Phe8397Leu
NM_182961.3:c.25335T>A NP_892006.3:p.Phe8445Leu
XM_006715407.1:c.25440T>A XP_006715470.1:p.Phe8480Leu
XM_006715408.1:c.25428T>A XP_006715471.1:p.Phe8476Leu
XM_006715409.1:c.25419T>A XP_006715472.1:p.Phe8473Leu
XM_006715410.1:c.25440T>A XP_006715473.1:p.Phe8480Leu
XM_006715411.1:c.25389T>A XP_006715474.1:p.Phe8463Leu
XM_006715412.1:c.25425T>A XP_006715475.1:p.Phe8475Leu
XM_006715413.1:c.25371T>A XP_006715476.1:p.Phe8457Leu
XM_006715414.1:c.25368T>A XP_006715477.1:p.Phe8456Leu
XM_006715415.1:c.25371T>A XP_006715478.1:p.Phe8457Leu
XM_006715416.1:c.25356T>A XP_006715479.1:p.Phe8452Leu
XM_006715417.1:c.25299T>A XP_006715480.1:p.Phe8433Leu
XM_006715420.1:c.25287T>A XP_006715483.1:p.Phe8429Leu
XM_006715421.1:c.25284T>A XP_006715484.1:p.Phe8428Leu
XM_006715422.1:c.25281T>A XP_006715485.1:p.Phe8427Leu
XM_006715423.1:c.25440T>A XP_006715486.1:p.Phe8480Leu
XM_006715424.1:c.25440T>A XP_006715487.1:p.Phe8480Leu
XM_006715425.1:c.25371T>A XP_006715488.1:p.Phe8457Leu
XM_011535641.1:c.25437T>A XP_011533943.1:p.Phe8479Leu
XM_011535642.1:c.25425T>A XP_011533944.1:p.Phe8475Leu
XM_011535643.1:c.25275T>A XP_011533945.1:p.Phe8425Leu
XM_011535644.1:c.23715T>A XP_011533946.1:p.Phe7905Leu
XM_011535645.1:c.23208T>A XP_011533947.1:p.Phe7736Leu
XM_011535647.1:c.18675T>A XP_011533949.1:p.Phe6225Leu
NM_001347701.1:c.1941T>A NP_001334630.1:p.Phe647Leu
NM_001347702.1:c.1869T>A NP_001334631.1:p.Phe623Leu
XM_006715408.2:c.25428T>A XP_006715471.1:p.Phe8476Leu
XM_006715410.2:c.25440T>A XP_006715473.1:p.Phe8480Leu
XM_006715412.2:c.25425T>A XP_006715475.1:p.Phe8475Leu
XM_006715413.2:c.25371T>A XP_006715476.1:p.Phe8457Leu
XM_006715415.2:c.25371T>A XP_006715478.1:p.Phe8457Leu
XM_006715416.2:c.25356T>A XP_006715479.1:p.Phe8452Leu
XM_006715417.2:c.25299T>A XP_006715480.1:p.Phe8433Leu
XM_006715420.2:c.25287T>A XP_006715483.1:p.Phe8429Leu
XM_006715421.2:c.25284T>A XP_006715484.1:p.Phe8428Leu
XM_006715423.2:c.25440T>A XP_006715486.1:p.Phe8480Leu
XM_006715424.2:c.25440T>A XP_006715487.1:p.Phe8480Leu
XM_006715425.2:c.25371T>A XP_006715488.1:p.Phe8457Leu
XM_011535641.2:c.25437T>A XP_011533943.1:p.Phe8479Leu
XM_011535642.2:c.25425T>A XP_011533944.1:p.Phe8475Leu
XM_011535645.2:c.23208T>A XP_011533947.1:p.Phe7736Leu
XM_017010608.1:c.25440T>A XP_016866097.1:p.Phe8480Leu
XM_017010609.1:c.25440T>A XP_016866098.1:p.Phe8480Leu
XM_017010610.1:c.25419T>A XP_016866099.1:p.Phe8473Leu
XM_017010611.2:c.25413T>A XP_016866100.1:p.Phe8471Leu
XM_017010612.1:c.25362T>A XP_016866101.1:p.Phe8454Leu
XM_017010613.1:c.25368T>A XP_016866102.1:p.Phe8456Leu
XM_017010614.1:c.25284T>A XP_016866103.1:p.Phe8428Leu
XM_017010615.1:c.25215T>A XP_016866104.1:p.Phe8405Leu
XM_017010616.1:c.25371T>A XP_016866105.1:p.Phe8457Leu
XM_017010617.1:c.25368T>A XP_016866106.1:p.Phe8456Leu
XM_017010618.1:c.25356T>A XP_016866107.1:p.Phe8452Leu
XM_017010619.1:c.23715T>A XP_016866108.1:p.Phe7905Leu
NM_182961.4:c.25335T>A MANE Select NP_892006.3:p.Phe8445Leu
NM_001347701.2:c.1941T>A NP_001334630.1:p.Phe647Leu
NM_001347702.2:c.1869T>A MANE Plus Clinical NP_001334631.1:p.Phe623Leu
NM_033071.5:c.25191T>A NP_149062.2:p.Phe8397Leu