Canonical Allele Identifier: CA2466480557

Gene: SSR4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798082T= , CM000685.2:g.153798082T=	GRCh38
NC_000023.10:g.153063537T= , CM000685.1:g.153063537T=	GRCh37
NC_000023.9:g.152716731T=	NCBI36
NG_041795.1:g.8908T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.363T= MANE Select	ENSP00000359103.3:p.Asn121=
ENST00000320857.7:c.363T=	ENSP00000317331.3:p.Asn121=
ENST00000370085.3:c.288T=	ENSP00000359102.3:p.Asn96=
ENST00000370086.7:c.363T=	ENSP00000359103.3:p.Asn121=
ENST00000370087.5:c.363T=	ENSP00000359104.1:p.Asn121=
ENST00000447375.1:n.203T=
ENST00000460616.5:n.2071T=
ENST00000471880.5:n.566T=
ENST00000482902.5:n.2190T=
ENST00000485612.5:n.478T=
ENST00000486204.5:n.435T=
NM_001204526.1:c.396T=	NP_001191455.1:p.Asn132=
NM_001204527.1:c.387T=	NP_001191456.1:p.Asn129=
NM_006280.2:c.363T=	NP_006271.1:p.Asn121=
NR_037927.1:n.708T=
XM_011531186.1:c.363T=	XP_011529488.1:p.Asn121=
XM_011531187.1:c.363T=	XP_011529489.1:p.Asn121=
XM_017029756.1:c.174T=	XP_016885245.1:p.Asn58=
XM_017029757.1:c.174T=	XP_016885246.1:p.Asn58=
XM_024452428.1:c.174T=	XP_024308196.1:p.Asn58=
NM_001204527.2:c.387T=	NP_001191456.1:p.Asn129=
NM_006280.3:c.363T= MANE Select	NP_006271.1:p.Asn121=