Canonical Allele Identifier: CA2241324543

Gene: GALNS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88835251G= , CM000678.2:g.88835251G=	GRCh38
NC_000016.9:g.88901659G= , CM000678.1:g.88901659G=	GRCh37
NC_000016.8:g.87429160G=	NCBI36
NG_008667.1:g.26716C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.860C= MANE Select	ENSP00000268695.5:p.Ser287=
ENST00000268695.9:c.860C=	ENSP00000268695.5:p.Ser287=
ENST00000562593.5:n.4269C=
ENST00000562931.5:n.448C=
ENST00000567525.5:c.541C=	ENSP00000454484.1:n.541C=
ENST00000568613.5:c.979C=	ENSP00000457921.1:n.979C=
NM_000512.4:c.860C=	NP_000503.1:p.Ser287=
XM_005256301.2:c.860C=	XP_005256358.1:p.Ser287=
XM_005256302.1:c.878C=	XP_005256359.1:p.Ser293=
XM_011522982.1:c.878C=	XP_011521284.1:p.Ser293=
XM_011522984.1:c.878C=	XP_011521286.1:p.Ser293=
NM_001323543.1:c.305C=	NP_001310472.1:p.Ser102=
NM_001323544.1:c.878C=	NP_001310473.1:p.Ser293=
XM_005256301.3:c.860C=	XP_005256358.1:p.Ser287=
XM_011522982.2:c.878C=	XP_011521284.1:p.Ser293=
XM_017023111.2:c.878C=	XP_016878600.1:p.Ser293=
XM_017023112.2:c.878C=	XP_016878601.1:p.Ser293=
XM_017023113.1:c.305C=	XP_016878602.1:p.Ser102=
NM_000512.5:c.860C= MANE Select	NP_000503.1:p.Ser287=
NM_001323543.2:c.305C=	NP_001310472.1:p.Ser102=
NM_001323544.2:c.878C=	NP_001310473.1:p.Ser293=