Canonical Allele Identifier: CA1304733148
Gene: GALNT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165759443A= , CM000664.2:g.165759443A= GRCh38
NC_000002.11:g.166615953A= , CM000664.1:g.166615953A= GRCh37
NC_000002.10:g.166324199A= NCBI36
NG_012069.1:g.39851T=

Transcript Alleles

HGVS Amino-acid Change
NM_004482.4:c.966T= MANE Select NP_004473.2:p.Tyr322=
ENST00000392701.8:c.966T= MANE Select ENSP00000376465.3:p.Tyr322=
NM_004482.3:c.966T= NP_004473.2:p.Tyr322=
ENST00000392701.7:c.966T= ENSP00000376465.3:p.Tyr322=
ENST00000409882.5:c.180T= ENSP00000386955.1:p.Tyr60=
ENST00000412248.5:c.966T= ENSP00000412643.1:p.Tyr322=
ENST00000437849.1:c.394T= ENSP00000391104.1:n.394T=
ENST00000463254.1:n.249T=
XM_005246449.1:c.966T= XP_005246506.1:p.Tyr322=
XM_006712402.2:c.966T= XP_006712465.1:p.Tyr322=
XM_011510929.1:c.966T= XP_011509231.1:p.Tyr322=
XM_017003770.1:c.966T= XP_016859259.1:p.Tyr322=
XR_002959253.1:n.1307T=