Canonical Allele Identifier: CA397094501

Gene: GALNS

Linked Data

• dbSNP Id: rs1909828056
• gnomAD v4: 16-88818088-C-A
• MyVariant Identifiers: chr16:g.88884496C>A (hg19) ; chr16:g.88818088C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88818088C>A , CM000678.2:g.88818088C>A	GRCh38
NC_000016.9:g.88884496C>A , CM000678.1:g.88884496C>A	GRCh37
NC_000016.8:g.87411997C>A	NCBI36
NG_008667.1:g.43879G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.1401G>T MANE Select	ENSP00000268695.5:p.Arg467Ser
ENST00000268695.9:c.1401G>T	ENSP00000268695.5:p.Arg467Ser
ENST00000562593.5:n.4810G>T
ENST00000567525.5:c.1082G>T	ENSP00000454484.1:n.1082G>T
ENST00000568613.5:c.1520G>T	ENSP00000457921.1:n.1520G>T
NM_000512.4:c.1401G>T	NP_000503.1:p.Arg467Ser
XM_005256301.2:c.1401G>T	XP_005256358.1:p.Arg467Ser
XM_005256302.1:c.1419G>T	XP_005256359.1:p.Arg473Ser
XM_011522982.1:c.1419G>T	XP_011521284.1:p.Arg473Ser
XM_011522984.1:c.1419G>T	XP_011521286.1:p.Arg473Ser
NM_001323543.1:c.846G>T	NP_001310472.1:p.Arg282Ser
NM_001323544.1:c.1419G>T	NP_001310473.1:p.Arg473Ser
XM_005256301.3:c.1401G>T	XP_005256358.1:p.Arg467Ser
XM_011522982.2:c.1419G>T	XP_011521284.1:p.Arg473Ser
XM_017023111.2:c.1419G>T	XP_016878600.1:p.Arg473Ser
XM_017023112.2:c.1419G>T	XP_016878601.1:p.Arg473Ser
XM_017023113.1:c.846G>T	XP_016878602.1:p.Arg282Ser
NM_000512.5:c.1401G>T MANE Select	NP_000503.1:p.Arg467Ser
NM_001323543.2:c.846G>T	NP_001310472.1:p.Arg282Ser
NM_001323544.2:c.1419G>T	NP_001310473.1:p.Arg473Ser