Canonical Allele Identifier: CA201629

Gene: GALNT3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165770569T>C , CM000664.2:g.165770569T>C	GRCh38
NC_000002.11:g.166627079T>C , CM000664.1:g.166627079T>C	GRCh37
NC_000002.10:g.166335325T>C	NCBI36
NG_012069.1:g.28725A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392701.8:c.132A>G MANE Select	ENSP00000376465.3:p.Gln44=
ENST00000392701.7:c.132A>G	ENSP00000376465.3:p.Gln44=
ENST00000412248.5:c.132A>G	ENSP00000412643.1:p.Gln44=
ENST00000414977.5:c.132A>G	ENSP00000413477.1:p.Gln44=
ENST00000431484.1:c.132A>G	ENSP00000397112.1:p.Gln44=
NM_004482.3:c.132A>G	NP_004473.2:p.Gln44=
XM_005246449.1:c.132A>G	XP_005246506.1:p.Gln44=
XM_006712402.2:c.132A>G	XP_006712465.1:p.Gln44=
XM_011510929.1:c.132A>G	XP_011509231.1:p.Gln44=
XM_017003770.1:c.132A>G	XP_016859259.1:p.Gln44=
XR_002959253.1:n.473A>G
NM_004482.4:c.132A>G MANE Select	NP_004473.2:p.Gln44=