Canonical Allele Identifier: CA2241324527

Gene: GALNS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88835226G= , CM000678.2:g.88835226G=	GRCh38
NC_000016.9:g.88901634G= , CM000678.1:g.88901634G=	GRCh37
NC_000016.8:g.87429135G=	NCBI36
NG_008667.1:g.26741C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.885C= MANE Select	ENSP00000268695.5:p.Ser295=
ENST00000268695.9:c.885C=	ENSP00000268695.5:p.Ser295=
ENST00000562593.5:n.4294C=
ENST00000562931.5:n.473C=
ENST00000567525.5:c.566C=	ENSP00000454484.1:n.566C=
ENST00000568613.5:c.1004C=	ENSP00000457921.1:n.1004C=
NM_000512.4:c.885C=	NP_000503.1:p.Ser295=
XM_005256301.2:c.885C=	XP_005256358.1:p.Ser295=
XM_005256302.1:c.903C=	XP_005256359.1:p.Ser301=
XM_011522982.1:c.903C=	XP_011521284.1:p.Ser301=
XM_011522984.1:c.903C=	XP_011521286.1:p.Ser301=
NM_001323543.1:c.330C=	NP_001310472.1:p.Ser110=
NM_001323544.1:c.903C=	NP_001310473.1:p.Ser301=
XM_005256301.3:c.885C=	XP_005256358.1:p.Ser295=
XM_011522982.2:c.903C=	XP_011521284.1:p.Ser301=
XM_017023111.2:c.903C=	XP_016878600.1:p.Ser301=
XM_017023112.2:c.903C=	XP_016878601.1:p.Ser301=
XM_017023113.1:c.330C=	XP_016878602.1:p.Ser110=
NM_000512.5:c.885C= MANE Select	NP_000503.1:p.Ser295=
NM_001323543.2:c.330C=	NP_001310472.1:p.Ser110=
NM_001323544.2:c.903C=	NP_001310473.1:p.Ser301=