Canonical Allele Identifier: CA397096415

Gene: GALNS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88822694G>C , CM000678.2:g.88822694G>C	GRCh38
NC_000016.9:g.88889102G>C , CM000678.1:g.88889102G>C	GRCh37
NC_000016.8:g.87416603G>C	NCBI36
NG_008667.1:g.39273C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000512.5:c.1259C>G MANE Select	NP_000503.1:p.Pro420Arg
ENST00000268695.10:c.1259C>G MANE Select	ENSP00000268695.5:p.Pro420Arg
NM_000512.4:c.1259C>G	NP_000503.1:p.Pro420Arg
NM_001323543.1:c.704C>G	NP_001310472.1:p.Pro235Arg
NM_001323543.2:c.704C>G	NP_001310472.1:p.Pro235Arg
NM_001323544.1:c.1277C>G	NP_001310473.1:p.Pro426Arg
NM_001323544.2:c.1277C>G	NP_001310473.1:p.Pro426Arg
ENST00000268695.9:c.1259C>G	ENSP00000268695.5:p.Pro420Arg
ENST00000562593.5:n.4668C>G
ENST00000567525.5:c.940C>G	ENSP00000454484.1:n.940C>G
ENST00000568613.5:c.1378C>G	ENSP00000457921.1:n.1378C>G
XM_005256301.2:c.1259C>G	XP_005256358.1:p.Pro420Arg
XM_005256301.3:c.1259C>G	XP_005256358.1:p.Pro420Arg
XM_005256302.1:c.1277C>G	XP_005256359.1:p.Pro426Arg
XM_011522982.1:c.1277C>G	XP_011521284.1:p.Pro426Arg
XM_011522982.2:c.1277C>G	XP_011521284.1:p.Pro426Arg
XM_011522984.1:c.1277C>G	XP_011521286.1:p.Pro426Arg
XM_017023111.2:c.1277C>G	XP_016878600.1:p.Pro426Arg
XM_017023112.2:c.1277C>G	XP_016878601.1:p.Pro426Arg
XM_017023113.1:c.704C>G	XP_016878602.1:p.Pro235Arg