Canonical Allele Identifier: CA2361424950

Gene: GSS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34936976T= , CM000682.2:g.34936976T=	GRCh38
NC_000020.10:g.33524779T= , CM000682.1:g.33524779T=	GRCh37
NC_000020.9:g.32988440T=	NCBI36
NG_008848.1:g.23823A=
NG_008848.2:g.24052A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000178.4:c.656A= MANE Select	NP_000169.1:p.Asp219=
ENST00000651619.1:c.656A= MANE Select	ENSP00000498303.1:p.Asp219=
NM_000178.2:c.656A=	NP_000169.1:p.Asp219=
NM_001322494.1:c.656A=	NP_001309423.1:p.Asp219=
NM_001322495.1:c.656A=	NP_001309424.1:p.Asp219=
ENST00000216951.6:c.656A=	ENSP00000216951.2:p.Asp219=
ENST00000451957.2:c.323A=	ENSP00000407517.2:p.Asp108=
ENST00000642493.1:c.*363A=	ENSP00000493524.1:n.*363A=
ENST00000642498.1:c.656A=	ENSP00000493631.1:p.Asp219=
ENST00000642538.1:c.399A=	ENSP00000493927.1:p.Ter133=
ENST00000643188.1:c.656A=	ENSP00000493903.1:p.Asp219=
ENST00000643443.1:c.*363A=	ENSP00000495572.1:n.*363A=
ENST00000643502.1:c.313A=
ENST00000643908.1:n.1019A=
ENST00000644538.1:n.933A=
ENST00000644793.1:c.656A=	ENSP00000495750.1:p.Asp219=
ENST00000645328.1:c.34A=
ENST00000645408.1:c.256A=
ENST00000645723.1:n.1895A=
ENST00000646405.1:c.*141A=	ENSP00000493744.1:n.*141A=
ENST00000646497.1:n.603A=
ENST00000646502.1:n.1138A=
ENST00000646512.1:n.869A=
ENST00000646735.1:c.323A=	ENSP00000493763.1:p.Asp108=
ENST00000646766.1:c.*286A=	ENSP00000494333.1:n.*286A=
XM_005260406.3:c.656A=	XP_005260463.1:p.Asp219=
XM_011528796.1:c.656A=	XP_011527098.1:p.Asp219=