Canonical Allele Identifier: CA397101085

Gene: GALNS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88832024A>G , CM000678.2:g.88832024A>G	GRCh38
NC_000016.9:g.88898432A>G , CM000678.1:g.88898432A>G	GRCh37
NC_000016.8:g.87425933A>G	NCBI36
NG_008667.1:g.29943T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.976T>C MANE Select	ENSP00000268695.5:p.Trp326Arg
ENST00000268695.9:c.976T>C	ENSP00000268695.5:p.Trp326Arg
ENST00000562593.5:n.4385T>C
ENST00000567525.5:c.657T>C	ENSP00000454484.1:n.657T>C
ENST00000568613.5:c.1095T>C	ENSP00000457921.1:n.1095T>C
NM_000512.4:c.976T>C	NP_000503.1:p.Trp326Arg
XM_005256301.2:c.976T>C	XP_005256358.1:p.Trp326Arg
XM_005256302.1:c.994T>C	XP_005256359.1:p.Trp332Arg
XM_011522982.1:c.994T>C	XP_011521284.1:p.Trp332Arg
XM_011522984.1:c.994T>C	XP_011521286.1:p.Trp332Arg
NM_001323543.1:c.421T>C	NP_001310472.1:p.Trp141Arg
NM_001323544.1:c.994T>C	NP_001310473.1:p.Trp332Arg
XM_005256301.3:c.976T>C	XP_005256358.1:p.Trp326Arg
XM_011522982.2:c.994T>C	XP_011521284.1:p.Trp332Arg
XM_017023111.2:c.994T>C	XP_016878600.1:p.Trp332Arg
XM_017023112.2:c.994T>C	XP_016878601.1:p.Trp332Arg
XM_017023113.1:c.421T>C	XP_016878602.1:p.Trp141Arg
NM_000512.5:c.976T>C MANE Select	NP_000503.1:p.Trp326Arg
NM_001323543.2:c.421T>C	NP_001310472.1:p.Trp141Arg
NM_001323544.2:c.994T>C	NP_001310473.1:p.Trp332Arg