Canonical Allele Identifier: CA2581803393
Gene: GALNT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165761940G= , CM000664.2:g.165761940G= GRCh38
NC_000002.11:g.166618450G= , CM000664.1:g.166618450G= GRCh37
NC_000002.10:g.166326696G= NCBI36
NG_012069.1:g.37354C=

Transcript Alleles

HGVS Amino-acid Change
NM_004482.4:c.803C= MANE Select NP_004473.2:p.Ala268=
ENST00000392701.8:c.803C= MANE Select ENSP00000376465.3:p.Ala268=
NM_004482.3:c.803C= NP_004473.2:p.Ala268=
ENST00000392701.7:c.803C= ENSP00000376465.3:p.Ala268=
ENST00000412248.5:c.803C= ENSP00000412643.1:p.Ala268=
ENST00000437849.1:c.191C= ENSP00000391104.1:p.Ala64=
ENST00000463254.1:n.86C=
XM_005246449.1:c.803C= XP_005246506.1:p.Ala268=
XM_006712402.2:c.803C= XP_006712465.1:p.Ala268=
XM_011510929.1:c.803C= XP_011509231.1:p.Ala268=
XM_017003770.1:c.803C= XP_016859259.1:p.Ala268=
XR_002959253.1:n.1144C=