Canonical Allele Identifier: CA397081258

Gene: GALNS

Linked Data

• MyVariant Identifiers: chr16:g.88902640C>G (hg19) ; chr16:g.88836232C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88836232C>G , CM000678.2:g.88836232C>G	GRCh38
NC_000016.9:g.88902640C>G , CM000678.1:g.88902640C>G	GRCh37
NC_000016.8:g.87430141C>G	NCBI36
NG_008667.1:g.25735G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000268695.10:c.602G>C MANE Select	ENSP00000268695.5:p.Gly201Ala
ENST00000268695.9:c.602G>C	ENSP00000268695.5:p.Gly201Ala
ENST00000562593.5:n.4011G>C
ENST00000562831.1:c.386G>C	ENSP00000455174.1:p.Gly129Ala
ENST00000562931.5:n.190G>C
ENST00000566563.1:n.304G>C
ENST00000567525.5:c.283G>C	ENSP00000454484.1:n.283G>C
ENST00000568613.5:c.721G>C	ENSP00000457921.1:n.721G>C
NM_000512.4:c.602G>C	NP_000503.1:p.Gly201Ala
XM_005256301.2:c.602G>C	XP_005256358.1:p.Gly201Ala
XM_005256302.1:c.620G>C	XP_005256359.1:p.Gly207Ala
XM_011522982.1:c.620G>C	XP_011521284.1:p.Gly207Ala
XM_011522984.1:c.620G>C	XP_011521286.1:p.Gly207Ala
NM_001323543.1:c.47G>C	NP_001310472.1:p.Gly16Ala
NM_001323544.1:c.620G>C	NP_001310473.1:p.Gly207Ala
XM_005256301.3:c.602G>C	XP_005256358.1:p.Gly201Ala
XM_011522982.2:c.620G>C	XP_011521284.1:p.Gly207Ala
XM_017023111.2:c.620G>C	XP_016878600.1:p.Gly207Ala
XM_017023112.2:c.620G>C	XP_016878601.1:p.Gly207Ala
XM_017023113.1:c.47G>C	XP_016878602.1:p.Gly16Ala
NM_000512.5:c.602G>C MANE Select	NP_000503.1:p.Gly201Ala
NM_001323543.2:c.47G>C	NP_001310472.1:p.Gly16Ala
NM_001323544.2:c.620G>C	NP_001310473.1:p.Gly207Ala