Canonical Allele Identifier: CA8235193

Gene: GALNS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88841084C>A , CM000678.2:g.88841084C>A	GRCh38
NC_000016.9:g.88907492C>A , CM000678.1:g.88907492C>A	GRCh37
NC_000016.8:g.87434993C>A	NCBI36
NG_008667.1:g.20883G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000512.5:c.330G>T MANE Select	NP_000503.1:p.Pro110=
ENST00000268695.10:c.330G>T MANE Select	ENSP00000268695.5:p.Pro110=
NM_000512.4:c.330G>T	NP_000503.1:p.Pro110=
NM_001323543.1:c.-226G>T	NP_001310472.1:n.-226G>T
NM_001323543.2:c.-226G>T	NP_001310472.1:n.-226G>T
NM_001323544.1:c.348G>T	NP_001310473.1:p.Pro116=
NM_001323544.2:c.348G>T	NP_001310473.1:p.Pro116=
ENST00000268695.9:c.330G>T	ENSP00000268695.5:p.Pro110=
ENST00000562593.5:n.3739G>T
ENST00000562831.1:c.114G>T	ENSP00000455174.1:p.Pro38=
ENST00000565364.1:n.465G>T
ENST00000567525.5:c.155G>T	ENSP00000454484.1:p.Arg52Leu
ENST00000567779.1:n.160G>T
ENST00000568613.5:c.449G>T	ENSP00000457921.1:n.449G>T
XM_005256301.2:c.330G>T	XP_005256358.1:p.Pro110=
XM_005256301.3:c.330G>T	XP_005256358.1:p.Pro110=
XM_005256302.1:c.348G>T	XP_005256359.1:p.Pro116=
XM_011522982.1:c.348G>T	XP_011521284.1:p.Pro116=
XM_011522982.2:c.348G>T	XP_011521284.1:p.Pro116=
XM_011522984.1:c.348G>T	XP_011521286.1:p.Pro116=
XM_017023111.2:c.348G>T	XP_016878600.1:p.Pro116=
XM_017023112.2:c.348G>T	XP_016878601.1:p.Pro116=
XM_017023113.1:c.-226G>T	XP_016878602.1:n.-226G>T