Canonical Allele Identifier: CA497077944

Gene: GALNS

Linked Data

• MyVariant Identifiers: chr16:g.88907420G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88841012G>A , CM000678.2:g.88841012G>A	GRCh38
NC_000016.9:g.88907420G>A , CM000678.1:g.88907420G>A	GRCh37
NC_000016.8:g.87434921G>A	NCBI36
NG_008667.1:g.20955C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.402C>T MANE Select	ENSP00000268695.5:p.Val134=
ENST00000268695.9:c.402C>T	ENSP00000268695.5:p.Val134=
ENST00000562593.5:n.3811C>T
ENST00000562831.1:c.186C>T	ENSP00000455174.1:p.Val62=
ENST00000565364.1:n.537C>T
ENST00000567525.5:c.227C>T	ENSP00000454484.1:n.227C>T
ENST00000567779.1:n.232C>T
ENST00000568613.5:c.521C>T	ENSP00000457921.1:n.521C>T
NM_000512.4:c.402C>T	NP_000503.1:p.Val134=
XM_005256301.2:c.402C>T	XP_005256358.1:p.Val134=
XM_005256302.1:c.420C>T	XP_005256359.1:p.Val140=
XM_011522982.1:c.420C>T	XP_011521284.1:p.Val140=
XM_011522984.1:c.420C>T	XP_011521286.1:p.Val140=
NM_001323543.1:c.-154C>T	NP_001310472.1:n.-154C>T
NM_001323544.1:c.420C>T	NP_001310473.1:p.Val140=
XM_005256301.3:c.402C>T	XP_005256358.1:p.Val134=
XM_011522982.2:c.420C>T	XP_011521284.1:p.Val140=
XM_017023111.2:c.420C>T	XP_016878600.1:p.Val140=
XM_017023112.2:c.420C>T	XP_016878601.1:p.Val140=
XM_017023113.1:c.-154C>T	XP_016878602.1:n.-154C>T
NM_000512.5:c.402C>T MANE Select	NP_000503.1:p.Val134=
NM_001323543.2:c.-154C>T	NP_001310472.1:n.-154C>T
NM_001323544.2:c.420C>T	NP_001310473.1:p.Val140=