Canonical Allele Identifier: CA1446399

Gene: GALNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230255312G>A , CM000663.2:g.230255312G>A	GRCh38
NC_000001.10:g.230391058G>A , CM000663.1:g.230391058G>A	GRCh37
NC_000001.9:g.228457681G>A	NCBI36
NG_011854.1:g.193103G>A
NG_011854.2:g.202524G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366672.5:c.1104G>A MANE Select	ENSP00000355632.4:p.Thr368=
ENST00000366672.4:c.1104G>A	ENSP00000355632.4:p.Thr368=
NM_001291866.1:c.990G>A	NP_001278795.1:p.Thr330=
NM_004481.4:c.1104G>A	NP_004472.1:p.Thr368=
XM_011544154.1:c.1032G>A	XP_011542456.1:p.Thr344=
XM_011544155.1:c.903G>A	XP_011542457.1:p.Thr301=
XM_017000963.2:c.1104G>A	XP_016856452.1:p.Thr368=
XM_017000964.2:c.1011G>A	XP_016856453.1:p.Thr337=
XM_017000965.1:c.990G>A	XP_016856454.1:p.Thr330=
XM_017000966.1:c.903G>A	XP_016856455.1:p.Thr301=
NM_004481.5:c.1104G>A MANE Select	NP_004472.1:p.Thr368=
NM_001291866.2:c.990G>A	NP_001278795.1:p.Thr330=