Canonical Allele Identifier: CA397088429
Community Standard Title: NM_000512.5(GALNS):c.320-1G>T
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88841095C>A , CM000678.2:g.88841095C>A GRCh38
NC_000016.9:g.88907503C>A , CM000678.1:g.88907503C>A GRCh37
NC_000016.8:g.87435004C>A NCBI36
NG_008667.1:g.20872G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000512.5:c.320-1G>T MANE Select NP_000503.1:n.320-1G>T
ENST00000268695.10:c.320-1G>T MANE Select ENSP00000268695.5:n.320-1G>T
NM_000512.4:c.320-1G>T NP_000503.1:n.320-1G>T
NM_001323543.1:c.-236-1G>T NP_001310472.1:n.-236-1G>T
NM_001323543.2:c.-236-1G>T NP_001310472.1:n.-236-1G>T
NM_001323544.1:c.338-1G>T NP_001310473.1:n.338-1G>T
NM_001323544.2:c.338-1G>T NP_001310473.1:n.338-1G>T
ENST00000268695.9:c.320-1G>T ENSP00000268695.5:n.320-1G>T
ENST00000562593.5:n.3729-1G>T
ENST00000562831.1:c.104-1G>T ENSP00000455174.1:n.104-1G>T
ENST00000565364.1:n.455-1G>T
ENST00000567525.5:c.145-1G>T ENSP00000454484.1:n.145-1G>T
ENST00000567779.1:n.150-1G>T
ENST00000568613.5:c.439-1G>T ENSP00000457921.1:n.439-1G>T
XM_005256301.2:c.320-1G>T XP_005256358.1:n.320-1G>T
XM_005256301.3:c.320-1G>T XP_005256358.1:n.320-1G>T
XM_005256302.1:c.338-1G>T XP_005256359.1:n.338-1G>T
XM_011522982.1:c.338-1G>T XP_011521284.1:n.338-1G>T
XM_011522982.2:c.338-1G>T XP_011521284.1:n.338-1G>T
XM_011522984.1:c.338-1G>T XP_011521286.1:n.338-1G>T
XM_017023111.2:c.338-1G>T XP_016878600.1:n.338-1G>T
XM_017023112.2:c.338-1G>T XP_016878601.1:n.338-1G>T
XM_017023113.1:c.-236-1G>T XP_016878602.1:n.-236-1G>T