Canonical Allele Identifier: CA2241324729

Gene: GALNS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88835559A= , CM000678.2:g.88835559A=	GRCh38
NC_000016.9:g.88901967A= , CM000678.1:g.88901967A=	GRCh37
NC_000016.8:g.87429468A=	NCBI36
NG_008667.1:g.26408T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.758+166T= MANE Select	ENSP00000268695.5:n.758+166T=
ENST00000268695.9:c.758+166T=	ENSP00000268695.5:n.758+166T=
ENST00000562593.5:n.4167+166T=
ENST00000562931.5:n.346+166T=
ENST00000567525.5:c.439+166T=	ENSP00000454484.1:n.439+166T=
ENST00000568613.5:c.877+166T=	ENSP00000457921.1:n.877+166T=
NM_000512.4:c.758+166T=	NP_000503.1:n.758+166T=
XM_005256301.2:c.758+166T=	XP_005256358.1:n.758+166T=
XM_005256302.1:c.776+166T=	XP_005256359.1:n.776+166T=
XM_011522982.1:c.776+166T=	XP_011521284.1:n.776+166T=
XM_011522984.1:c.776+166T=	XP_011521286.1:n.776+166T=
NM_001323543.1:c.203+166T=	NP_001310472.1:n.203+166T=
NM_001323544.1:c.776+166T=	NP_001310473.1:n.776+166T=
XM_005256301.3:c.758+166T=	XP_005256358.1:n.758+166T=
XM_011522982.2:c.776+166T=	XP_011521284.1:n.776+166T=
XM_017023111.2:c.776+166T=	XP_016878600.1:n.776+166T=
XM_017023112.2:c.776+166T=	XP_016878601.1:n.776+166T=
XM_017023113.1:c.203+166T=	XP_016878602.1:n.203+166T=
NM_000512.5:c.758+166T= MANE Select	NP_000503.1:n.758+166T=
NM_001323543.2:c.203+166T=	NP_001310472.1:n.203+166T=
NM_001323544.2:c.776+166T=	NP_001310473.1:n.776+166T=