Canonical Allele Identifier: CA397087506

Gene: GALNS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88840991C>T , CM000678.2:g.88840991C>T	GRCh38
NC_000016.9:g.88907399C>T , CM000678.1:g.88907399C>T	GRCh37
NC_000016.8:g.87434900C>T	NCBI36
NG_008667.1:g.20976G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000512.5:c.422+1G>A MANE Select	NP_000503.1:n.422+1G>A
ENST00000268695.10:c.422+1G>A MANE Select	ENSP00000268695.5:n.422+1G>A
NM_000512.4:c.422+1G>A	NP_000503.1:n.422+1G>A
NM_001323543.1:c.-134+1G>A	NP_001310472.1:n.-134+1G>A
NM_001323543.2:c.-134+1G>A	NP_001310472.1:n.-134+1G>A
NM_001323544.1:c.440+1G>A	NP_001310473.1:n.440+1G>A
NM_001323544.2:c.440+1G>A	NP_001310473.1:n.440+1G>A
ENST00000268695.9:c.422+1G>A	ENSP00000268695.5:n.422+1G>A
ENST00000562593.5:n.3831+1G>A
ENST00000562831.1:c.206+1G>A	ENSP00000455174.1:n.206+1G>A
ENST00000565364.1:n.557+1G>A
ENST00000567525.5:c.247+1G>A	ENSP00000454484.1:n.247+1G>A
ENST00000567779.1:n.253G>A
ENST00000568613.5:c.541+1G>A	ENSP00000457921.1:n.541+1G>A
XM_005256301.2:c.422+1G>A	XP_005256358.1:n.422+1G>A
XM_005256301.3:c.422+1G>A	XP_005256358.1:n.422+1G>A
XM_005256302.1:c.440+1G>A	XP_005256359.1:n.440+1G>A
XM_011522982.1:c.440+1G>A	XP_011521284.1:n.440+1G>A
XM_011522982.2:c.440+1G>A	XP_011521284.1:n.440+1G>A
XM_011522984.1:c.440+1G>A	XP_011521286.1:n.440+1G>A
XM_017023111.2:c.440+1G>A	XP_016878600.1:n.440+1G>A
XM_017023112.2:c.440+1G>A	XP_016878601.1:n.440+1G>A
XM_017023113.1:c.-134+1G>A	XP_016878602.1:n.-134+1G>A