Canonical Allele Identifier: CA366086936
Gene: SYNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152152013G>T , CM000668.2:g.152152013G>T GRCh38
NC_000006.11:g.152473148G>T , CM000668.1:g.152473148G>T GRCh37
NC_000006.10:g.152514841G>T NCBI36
NG_012855.1:g.490387C>A
NG_012855.2:g.490387C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.723C>A MANE Plus Clinical ENSP00000346701.4:p.Asn241Lys
ENST00000367255.10:c.24258C>A MANE Select ENSP00000356224.5:p.Asn8086Lys
ENST00000423061.6:c.24045C>A ENSP00000396024.1:p.Asn8015Lys
ENST00000673173.1:c.172C>A
ENST00000673451.1:c.30C>A ENSP00000500189.1:p.Asn10Lys
ENST00000341594.9:c.23043C>A ENSP00000341887.6:p.Asn7681Lys
ENST00000347037.9:n.937C>A
ENST00000354674.4:c.723C>A ENSP00000346701.4:p.Asn241Lys
ENST00000367251.7:c.3024C>A ENSP00000356220.3:p.Asn1008Lys
ENST00000367255.9:c.24258C>A ENSP00000356224.5:p.Asn8086Lys
ENST00000367256.9:n.7950C>A
ENST00000367257.8:c.2196C>A ENSP00000356226.4:p.Asn732Lys
ENST00000409694.6:n.7842C>A
ENST00000423061.5:c.24045C>A ENSP00000396024.1:p.Asn8015Lys
ENST00000460912.6:n.803C>A
ENST00000476519.1:n.320C>A
ENST00000536990.5:n.1095C>A
ENST00000539504.5:c.723C>A ENSP00000441052.1:p.Asn241Lys
NM_033071.3:c.24045C>A NP_149062.1:p.Asn8015Lys
NM_182961.3:c.24258C>A NP_892006.3:p.Asn8086Lys
XM_006715407.1:c.24294C>A XP_006715470.1:p.Asn8098Lys
XM_006715408.1:c.24282C>A XP_006715471.1:p.Asn8094Lys
XM_006715409.1:c.24273C>A XP_006715472.1:p.Asn8091Lys
XM_006715410.1:c.24294C>A XP_006715473.1:p.Asn8098Lys
XM_006715411.1:c.24243C>A XP_006715474.1:p.Asn8081Lys
XM_006715412.1:c.24279C>A XP_006715475.1:p.Asn8093Lys
XM_006715413.1:c.24294C>A XP_006715476.1:p.Asn8098Lys
XM_006715414.1:c.24222C>A XP_006715477.1:p.Asn8074Lys
XM_006715415.1:c.24294C>A XP_006715478.1:p.Asn8098Lys
XM_006715416.1:c.24279C>A XP_006715479.1:p.Asn8093Lys
XM_006715417.1:c.24153C>A XP_006715480.1:p.Asn8051Lys
XM_006715420.1:c.24141C>A XP_006715483.1:p.Asn8047Lys
XM_006715421.1:c.24138C>A XP_006715484.1:p.Asn8046Lys
XM_006715422.1:c.24135C>A XP_006715485.1:p.Asn8045Lys
XM_006715423.1:c.24294C>A XP_006715486.1:p.Asn8098Lys
XM_006715424.1:c.24294C>A XP_006715487.1:p.Asn8098Lys
XM_006715425.1:c.24294C>A XP_006715488.1:p.Asn8098Lys
XM_011535641.1:c.24291C>A XP_011533943.1:p.Asn8097Lys
XM_011535642.1:c.24279C>A XP_011533944.1:p.Asn8093Lys
XM_011535643.1:c.24129C>A XP_011533945.1:p.Asn8043Lys
XM_011535644.1:c.22569C>A XP_011533946.1:p.Asn7523Lys
XM_011535645.1:c.22062C>A XP_011533947.1:p.Asn7354Lys
XM_011535647.1:c.17529C>A XP_011533949.1:p.Asn5843Lys
NM_001347701.1:c.864C>A NP_001334630.1:p.Asn288Lys
NM_001347702.1:c.723C>A NP_001334631.1:p.Asn241Lys
XM_006715408.2:c.24282C>A XP_006715471.1:p.Asn8094Lys
XM_006715410.2:c.24294C>A XP_006715473.1:p.Asn8098Lys
XM_006715412.2:c.24279C>A XP_006715475.1:p.Asn8093Lys
XM_006715413.2:c.24294C>A XP_006715476.1:p.Asn8098Lys
XM_006715415.2:c.24294C>A XP_006715478.1:p.Asn8098Lys
XM_006715416.2:c.24279C>A XP_006715479.1:p.Asn8093Lys
XM_006715417.2:c.24153C>A XP_006715480.1:p.Asn8051Lys
XM_006715420.2:c.24141C>A XP_006715483.1:p.Asn8047Lys
XM_006715421.2:c.24138C>A XP_006715484.1:p.Asn8046Lys
XM_006715423.2:c.24294C>A XP_006715486.1:p.Asn8098Lys
XM_006715424.2:c.24294C>A XP_006715487.1:p.Asn8098Lys
XM_006715425.2:c.24294C>A XP_006715488.1:p.Asn8098Lys
XM_011535641.2:c.24291C>A XP_011533943.1:p.Asn8097Lys
XM_011535642.2:c.24279C>A XP_011533944.1:p.Asn8093Lys
XM_011535645.2:c.22062C>A XP_011533947.1:p.Asn7354Lys
XM_017010608.1:c.24294C>A XP_016866097.1:p.Asn8098Lys
XM_017010609.1:c.24294C>A XP_016866098.1:p.Asn8098Lys
XM_017010610.1:c.24273C>A XP_016866099.1:p.Asn8091Lys
XM_017010611.2:c.24267C>A XP_016866100.1:p.Asn8089Lys
XM_017010612.1:c.24216C>A XP_016866101.1:p.Asn8072Lys
XM_017010613.1:c.24291C>A XP_016866102.1:p.Asn8097Lys
XM_017010614.1:c.24138C>A XP_016866103.1:p.Asn8046Lys
XM_017010615.1:c.24138C>A XP_016866104.1:p.Asn8046Lys
XM_017010616.1:c.24294C>A XP_016866105.1:p.Asn8098Lys
XM_017010617.1:c.24291C>A XP_016866106.1:p.Asn8097Lys
XM_017010618.1:c.24279C>A XP_016866107.1:p.Asn8093Lys
XM_017010619.1:c.22569C>A XP_016866108.1:p.Asn7523Lys
NM_182961.4:c.24258C>A MANE Select NP_892006.3:p.Asn8086Lys
NM_001347701.2:c.864C>A NP_001334630.1:p.Asn288Lys
NM_001347702.2:c.723C>A MANE Plus Clinical NP_001334631.1:p.Asn241Lys
NM_033071.5:c.24045C>A NP_149062.2:p.Asn8015Lys