Canonical Allele Identifier: CA2466480574

Gene: SSR4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798125G= , CM000685.2:g.153798125G=	GRCh38
NC_000023.10:g.153063580G= , CM000685.1:g.153063580G=	GRCh37
NC_000023.9:g.152716774G=	NCBI36
NG_041795.1:g.8951G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.406G= MANE Select	ENSP00000359103.3:p.Val136=
ENST00000320857.7:c.406G=	ENSP00000317331.3:p.Val136=
ENST00000370085.3:c.331G=	ENSP00000359102.3:p.Val111=
ENST00000370086.7:c.406G=	ENSP00000359103.3:p.Val136=
ENST00000370087.5:c.406G=	ENSP00000359104.1:p.Val136=
ENST00000447375.1:n.246G=
ENST00000460616.5:n.2114G=
ENST00000471880.5:n.609G=
ENST00000482902.5:n.2233G=
ENST00000485612.5:n.521G=
ENST00000486204.5:n.478G=
NM_001204526.1:c.439G=	NP_001191455.1:p.Val147=
NM_001204527.1:c.430G=	NP_001191456.1:p.Val144=
NM_006280.2:c.406G=	NP_006271.1:p.Val136=
NR_037927.1:n.751G=
XM_011531186.1:c.406G=	XP_011529488.1:p.Val136=
XM_011531187.1:c.406G=	XP_011529489.1:p.Val136=
XM_017029756.1:c.217G=	XP_016885245.1:p.Val73=
XM_017029757.1:c.217G=	XP_016885246.1:p.Val73=
XM_024452428.1:c.217G=	XP_024308196.1:p.Val73=
NM_001204527.2:c.430G=	NP_001191456.1:p.Val144=
NM_006280.3:c.406G= MANE Select	NP_006271.1:p.Val136=