Canonical Allele Identifier: CA397076034

Gene: GALNS

Linked Data

• ClinVar Variation Id: 1048427
• ClinVar RCV Id: RCV001578529
• dbSNP Id: rs975409254
• MyVariant Identifiers: chr16:g.88901651C>G (hg19) ; chr16:g.88835243C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88835243C>G , CM000678.2:g.88835243C>G	GRCh38
NC_000016.9:g.88901651C>G , CM000678.1:g.88901651C>G	GRCh37
NC_000016.8:g.87429152C>G	NCBI36
NG_008667.1:g.26724G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.868G>C MANE Select	ENSP00000268695.5:p.Gly290Arg
ENST00000268695.9:c.868G>C	ENSP00000268695.5:p.Gly290Arg
ENST00000562593.5:n.4277G>C
ENST00000562931.5:n.456G>C
ENST00000567525.5:c.549G>C	ENSP00000454484.1:n.549G>C
ENST00000568613.5:c.987G>C	ENSP00000457921.1:n.987G>C
NM_000512.4:c.868G>C	NP_000503.1:p.Gly290Arg
XM_005256301.2:c.868G>C	XP_005256358.1:p.Gly290Arg
XM_005256302.1:c.886G>C	XP_005256359.1:p.Gly296Arg
XM_011522982.1:c.886G>C	XP_011521284.1:p.Gly296Arg
XM_011522984.1:c.886G>C	XP_011521286.1:p.Gly296Arg
NM_001323543.1:c.313G>C	NP_001310472.1:p.Gly105Arg
NM_001323544.1:c.886G>C	NP_001310473.1:p.Gly296Arg
XM_005256301.3:c.868G>C	XP_005256358.1:p.Gly290Arg
XM_011522982.2:c.886G>C	XP_011521284.1:p.Gly296Arg
XM_017023111.2:c.886G>C	XP_016878600.1:p.Gly296Arg
XM_017023112.2:c.886G>C	XP_016878601.1:p.Gly296Arg
XM_017023113.1:c.313G>C	XP_016878602.1:p.Gly105Arg
NM_000512.5:c.868G>C MANE Select	NP_000503.1:p.Gly290Arg
NM_001323543.2:c.313G>C	NP_001310472.1:p.Gly105Arg
NM_001323544.2:c.886G>C	NP_001310473.1:p.Gly296Arg