Canonical Allele Identifier: CA2241328033

Gene: GALNS

Linked Data

• dbSNP Id: rs1966933744

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88840898T>G , CM000678.2:g.88840898T>G	GRCh38
NC_000016.9:g.88907306T>G , CM000678.1:g.88907306T>G	GRCh37
NC_000016.8:g.87434807T>G	NCBI36
NG_008667.1:g.21069A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.422+94A>C MANE Select	ENSP00000268695.5:n.422+94A>C
ENST00000268695.9:c.422+94A>C	ENSP00000268695.5:n.422+94A>C
ENST00000562593.5:n.3831+94A>C
ENST00000562831.1:c.206+94A>C	ENSP00000455174.1:n.206+94A>C
ENST00000565364.1:n.558-46A>C
ENST00000567525.5:c.247+94A>C	ENSP00000454484.1:n.247+94A>C
ENST00000567779.1:n.346A>C
ENST00000568613.5:c.541+94A>C	ENSP00000457921.1:n.541+94A>C
NM_000512.4:c.422+94A>C	NP_000503.1:n.422+94A>C
XM_005256301.2:c.422+94A>C	XP_005256358.1:n.422+94A>C
XM_005256302.1:c.440+94A>C	XP_005256359.1:n.440+94A>C
XM_011522982.1:c.440+94A>C	XP_011521284.1:n.440+94A>C
XM_011522984.1:c.440+94A>C	XP_011521286.1:n.440+94A>C
NM_001323543.1:c.-134+94A>C	NP_001310472.1:n.-134+94A>C
NM_001323544.1:c.440+94A>C	NP_001310473.1:n.440+94A>C
XM_005256301.3:c.422+94A>C	XP_005256358.1:n.422+94A>C
XM_011522982.2:c.440+94A>C	XP_011521284.1:n.440+94A>C
XM_017023111.2:c.440+94A>C	XP_016878600.1:n.440+94A>C
XM_017023112.2:c.440+94A>C	XP_016878601.1:n.440+94A>C
XM_017023113.1:c.-134+94A>C	XP_016878602.1:n.-134+94A>C
NM_000512.5:c.422+94A>C MANE Select	NP_000503.1:n.422+94A>C
NM_001323543.2:c.-134+94A>C	NP_001310472.1:n.-134+94A>C
NM_001323544.2:c.440+94A>C	NP_001310473.1:n.440+94A>C