Canonical Allele Identifier: CA2466480565

Gene: SSR4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153798098A= , CM000685.2:g.153798098A=	GRCh38
NC_000023.10:g.153063553A= , CM000685.1:g.153063553A=	GRCh37
NC_000023.9:g.152716747A=	NCBI36
NG_041795.1:g.8924A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.379A= MANE Select	ENSP00000359103.3:p.Ile127=
ENST00000320857.7:c.379A=	ENSP00000317331.3:p.Ile127=
ENST00000370085.3:c.304A=	ENSP00000359102.3:p.Ile102=
ENST00000370086.7:c.379A=	ENSP00000359103.3:p.Ile127=
ENST00000370087.5:c.379A=	ENSP00000359104.1:p.Ile127=
ENST00000447375.1:n.219A=
ENST00000460616.5:n.2087A=
ENST00000471880.5:n.582A=
ENST00000482902.5:n.2206A=
ENST00000485612.5:n.494A=
ENST00000486204.5:n.451A=
NM_001204526.1:c.412A=	NP_001191455.1:p.Ile138=
NM_001204527.1:c.403A=	NP_001191456.1:p.Ile135=
NM_006280.2:c.379A=	NP_006271.1:p.Ile127=
NR_037927.1:n.724A=
XM_011531186.1:c.379A=	XP_011529488.1:p.Ile127=
XM_011531187.1:c.379A=	XP_011529489.1:p.Ile127=
XM_017029756.1:c.190A=	XP_016885245.1:p.Ile64=
XM_017029757.1:c.190A=	XP_016885246.1:p.Ile64=
XM_024452428.1:c.190A=	XP_024308196.1:p.Ile64=
NM_001204527.2:c.403A=	NP_001191456.1:p.Ile135=
NM_006280.3:c.379A= MANE Select	NP_006271.1:p.Ile127=