Canonical Allele Identifier: CA2466480564

Gene: SSR4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798096C= , CM000685.2:g.153798096C=	GRCh38
NC_000023.10:g.153063551C= , CM000685.1:g.153063551C=	GRCh37
NC_000023.9:g.152716745C=	NCBI36
NG_041795.1:g.8922C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.377C= MANE Select	ENSP00000359103.3:p.Ser126=
ENST00000320857.7:c.377C=	ENSP00000317331.3:p.Ser126=
ENST00000370085.3:c.302C=	ENSP00000359102.3:p.Ser101=
ENST00000370086.7:c.377C=	ENSP00000359103.3:p.Ser126=
ENST00000370087.5:c.377C=	ENSP00000359104.1:p.Ser126=
ENST00000447375.1:n.217C=
ENST00000460616.5:n.2085C=
ENST00000471880.5:n.580C=
ENST00000482902.5:n.2204C=
ENST00000485612.5:n.492C=
ENST00000486204.5:n.449C=
NM_001204526.1:c.410C=	NP_001191455.1:p.Ser137=
NM_001204527.1:c.401C=	NP_001191456.1:p.Ser134=
NM_006280.2:c.377C=	NP_006271.1:p.Ser126=
NR_037927.1:n.722C=
XM_011531186.1:c.377C=	XP_011529488.1:p.Ser126=
XM_011531187.1:c.377C=	XP_011529489.1:p.Ser126=
XM_017029756.1:c.188C=	XP_016885245.1:p.Ser63=
XM_017029757.1:c.188C=	XP_016885246.1:p.Ser63=
XM_024452428.1:c.188C=	XP_024308196.1:p.Ser63=
NM_001204527.2:c.401C=	NP_001191456.1:p.Ser134=
NM_006280.3:c.377C= MANE Select	NP_006271.1:p.Ser126=