Canonical Allele Identifier: CA397081267

Gene: GALNS

Linked Data

• MyVariant Identifiers: chr16:g.88902641C>A (hg19) ; chr16:g.88836233C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88836233C>A , CM000678.2:g.88836233C>A	GRCh38
NC_000016.9:g.88902641C>A , CM000678.1:g.88902641C>A	GRCh37
NC_000016.8:g.87430142C>A	NCBI36
NG_008667.1:g.25734G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000268695.10:c.601G>T MANE Select	ENSP00000268695.5:p.Gly201Trp
ENST00000268695.9:c.601G>T	ENSP00000268695.5:p.Gly201Trp
ENST00000562593.5:n.4010G>T
ENST00000562831.1:c.385G>T	ENSP00000455174.1:p.Gly129Trp
ENST00000562931.5:n.189G>T
ENST00000566563.1:n.303G>T
ENST00000567525.5:c.282G>T	ENSP00000454484.1:n.282G>T
ENST00000568613.5:c.720G>T	ENSP00000457921.1:n.720G>T
NM_000512.4:c.601G>T	NP_000503.1:p.Gly201Trp
XM_005256301.2:c.601G>T	XP_005256358.1:p.Gly201Trp
XM_005256302.1:c.619G>T	XP_005256359.1:p.Gly207Trp
XM_011522982.1:c.619G>T	XP_011521284.1:p.Gly207Trp
XM_011522984.1:c.619G>T	XP_011521286.1:p.Gly207Trp
NM_001323543.1:c.46G>T	NP_001310472.1:p.Gly16Trp
NM_001323544.1:c.619G>T	NP_001310473.1:p.Gly207Trp
XM_005256301.3:c.601G>T	XP_005256358.1:p.Gly201Trp
XM_011522982.2:c.619G>T	XP_011521284.1:p.Gly207Trp
XM_017023111.2:c.619G>T	XP_016878600.1:p.Gly207Trp
XM_017023112.2:c.619G>T	XP_016878601.1:p.Gly207Trp
XM_017023113.1:c.46G>T	XP_016878602.1:p.Gly16Trp
NM_000512.5:c.601G>T MANE Select	NP_000503.1:p.Gly201Trp
NM_001323543.2:c.46G>T	NP_001310472.1:p.Gly16Trp
NM_001323544.2:c.619G>T	NP_001310473.1:p.Gly207Trp