Canonical Allele Identifier: CA2466480562

Gene: SSR4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798091C= , CM000685.2:g.153798091C=	GRCh38
NC_000023.10:g.153063546C= , CM000685.1:g.153063546C=	GRCh37
NC_000023.9:g.152716740C=	NCBI36
NG_041795.1:g.8917C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.372C= MANE Select	ENSP00000359103.3:p.Asp124=
ENST00000320857.7:c.372C=	ENSP00000317331.3:p.Asp124=
ENST00000370085.3:c.297C=	ENSP00000359102.3:p.Asp99=
ENST00000370086.7:c.372C=	ENSP00000359103.3:p.Asp124=
ENST00000370087.5:c.372C=	ENSP00000359104.1:p.Asp124=
ENST00000447375.1:n.212C=
ENST00000460616.5:n.2080C=
ENST00000471880.5:n.575C=
ENST00000482902.5:n.2199C=
ENST00000485612.5:n.487C=
ENST00000486204.5:n.444C=
NM_001204526.1:c.405C=	NP_001191455.1:p.Asp135=
NM_001204527.1:c.396C=	NP_001191456.1:p.Asp132=
NM_006280.2:c.372C=	NP_006271.1:p.Asp124=
NR_037927.1:n.717C=
XM_011531186.1:c.372C=	XP_011529488.1:p.Asp124=
XM_011531187.1:c.372C=	XP_011529489.1:p.Asp124=
XM_017029756.1:c.183C=	XP_016885245.1:p.Asp61=
XM_017029757.1:c.183C=	XP_016885246.1:p.Asp61=
XM_024452428.1:c.183C=	XP_024308196.1:p.Asp61=
NM_001204527.2:c.396C=	NP_001191456.1:p.Asp132=
NM_006280.3:c.372C= MANE Select	NP_006271.1:p.Asp124=