Canonical Allele Identifier: CA2333925811

Gene: SYNE4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006404_36006405delinsCA , CM000681.2:g.36006404_36006405delinsCA	GRCh38
NC_000019.9:g.36497306_36497307delinsCA , CM000681.1:g.36497306_36497307delinsCA	GRCh37
NC_000019.8:g.41189146_41189147delinsCA	NCBI36
NG_042831.1:g.7389_7390delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.867+18_867+19delinsTG MANE Select	ENSP00000316130.3:n.867+18_867+19delinsTG
ENST00000397428.8:c.67-968_67-967delinsTG
ENST00000465425.2:n.997_998delinsTG
ENST00000324444.7:c.867+18_867+19delinsTG	ENSP00000316130.3:n.867+18_867+19delinsTG
ENST00000340477.9:c.528+18_528+19delinsTG	ENSP00000343152.5:n.528+18_528+19delinsTG
ENST00000397428.7:c.40-968_40-967delinsTG	ENSP00000380572.3:n.40-968_40-967delinsTG
ENST00000465425.1:n.997_998delinsTG
ENST00000490730.1:c.688+197_688+198delinsTG	ENSP00000422716.1:n.688+197_688+198delinsTG
ENST00000503121.5:c.242+1812_242+1813delinsTG
ENST00000505054.2:n.395-968_395-967delinsTG
NM_001039876.1:c.867+18_867+19delinsTG	NP_001034965.1:n.867+18_867+19delinsTG
NM_001039876.2:c.867+18_867+19delinsTG	NP_001034965.1:n.867+18_867+19delinsTG
NM_001297735.1:c.528+18_528+19delinsTG	NP_001284664.1:n.528+18_528+19delinsTG
NM_001297735.2:c.528+18_528+19delinsTG	NP_001284664.1:n.528+18_528+19delinsTG
XM_005258598.2:c.688+197_688+198delinsTG	XP_005258655.1:n.688+197_688+198delinsTG
XM_005258601.2:c.618+345_618+346delinsTG	XP_005258658.1:n.618+345_618+346delinsTG
XM_005258604.3:c.688+197_688+198delinsTG	XP_005258661.1:n.688+197_688+198delinsTG
NM_001039876.3:c.867+18_867+19delinsTG MANE Select	NP_001034965.1:n.867+18_867+19delinsTG
NM_001297735.3:c.528+18_528+19delinsTG	NP_001284664.1:n.528+18_528+19delinsTG