Canonical Allele Identifier: CA397089370

Gene: GALNS

Linked Data

• MyVariant Identifiers: chr16:g.88908367A>T (hg19) ; chr16:g.88841959A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88841959A>T , CM000678.2:g.88841959A>T	GRCh38
NC_000016.9:g.88908367A>T , CM000678.1:g.88908367A>T	GRCh37
NC_000016.8:g.87435868A>T	NCBI36
NG_008667.1:g.20008T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000268695.10:c.257T>A MANE Select	ENSP00000268695.5:p.Leu86Gln
ENST00000268695.9:c.257T>A	ENSP00000268695.5:p.Leu86Gln
ENST00000562593.5:n.3666T>A
ENST00000562831.1:c.41T>A	ENSP00000455174.1:p.Leu14Gln
ENST00000565364.1:n.392T>A
ENST00000567525.5:c.82T>A	ENSP00000454484.1:p.Cys28Ser
ENST00000567779.1:n.87T>A
ENST00000568613.5:c.376T>A	ENSP00000457921.1:n.376T>A
NM_000512.4:c.257T>A	NP_000503.1:p.Leu86Gln
XM_005256301.2:c.257T>A	XP_005256358.1:p.Leu86Gln
XM_005256302.1:c.275T>A	XP_005256359.1:p.Leu92Gln
XM_011522982.1:c.275T>A	XP_011521284.1:p.Leu92Gln
XM_011522984.1:c.275T>A	XP_011521286.1:p.Leu92Gln
NM_001323543.1:c.-299T>A	NP_001310472.1:n.-299T>A
NM_001323544.1:c.275T>A	NP_001310473.1:p.Leu92Gln
XM_005256301.3:c.257T>A	XP_005256358.1:p.Leu86Gln
XM_011522982.2:c.275T>A	XP_011521284.1:p.Leu92Gln
XM_017023111.2:c.275T>A	XP_016878600.1:p.Leu92Gln
XM_017023112.2:c.275T>A	XP_016878601.1:p.Leu92Gln
XM_017023113.1:c.-299T>A	XP_016878602.1:n.-299T>A
NM_000512.5:c.257T>A MANE Select	NP_000503.1:p.Leu86Gln
NM_001323543.2:c.-299T>A	NP_001310472.1:n.-299T>A
NM_001323544.2:c.275T>A	NP_001310473.1:p.Leu92Gln