Canonical Allele Identifier: CA2241325039

Gene: GALNS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88836032T= , CM000678.2:g.88836032T=	GRCh38
NC_000016.9:g.88902440T= , CM000678.1:g.88902440T=	GRCh37
NC_000016.8:g.87429941T=	NCBI36
NG_008667.1:g.25935A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.633+169A= MANE Select	ENSP00000268695.5:n.633+169A=
ENST00000268695.9:c.633+169A=	ENSP00000268695.5:n.633+169A=
ENST00000562593.5:n.4042+169A=
ENST00000562831.1:c.417+169A=	ENSP00000455174.1:n.417+169A=
ENST00000562931.5:n.221+169A=
ENST00000566563.1:n.335+169A=
ENST00000567525.5:c.314+169A=	ENSP00000454484.1:n.314+169A=
ENST00000568613.5:c.752+169A=	ENSP00000457921.1:n.752+169A=
NM_000512.4:c.633+169A=	NP_000503.1:n.633+169A=
XM_005256301.2:c.633+169A=	XP_005256358.1:n.633+169A=
XM_005256302.1:c.651+169A=	XP_005256359.1:n.651+169A=
XM_011522982.1:c.651+169A=	XP_011521284.1:n.651+169A=
XM_011522984.1:c.651+169A=	XP_011521286.1:n.651+169A=
NM_001323543.1:c.78+169A=	NP_001310472.1:n.78+169A=
NM_001323544.1:c.651+169A=	NP_001310473.1:n.651+169A=
XM_005256301.3:c.633+169A=	XP_005256358.1:n.633+169A=
XM_011522982.2:c.651+169A=	XP_011521284.1:n.651+169A=
XM_017023111.2:c.651+169A=	XP_016878600.1:n.651+169A=
XM_017023112.2:c.651+169A=	XP_016878601.1:n.651+169A=
XM_017023113.1:c.78+169A=	XP_016878602.1:n.78+169A=
NM_000512.5:c.633+169A= MANE Select	NP_000503.1:n.633+169A=
NM_001323543.2:c.78+169A=	NP_001310472.1:n.78+169A=
NM_001323544.2:c.651+169A=	NP_001310473.1:n.651+169A=