Canonical Allele Identifier: CA1304733264
Gene: GALNT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165761928G= , CM000664.2:g.165761928G= GRCh38
NC_000002.11:g.166618438G= , CM000664.1:g.166618438G= GRCh37
NC_000002.10:g.166326684G= NCBI36
NG_012069.1:g.37366C=

Transcript Alleles

HGVS Amino-acid Change
NM_004482.4:c.815C= MANE Select NP_004473.2:p.Thr272=
ENST00000392701.8:c.815C= MANE Select ENSP00000376465.3:p.Thr272=
NM_004482.3:c.815C= NP_004473.2:p.Thr272=
ENST00000392701.7:c.815C= ENSP00000376465.3:p.Thr272=
ENST00000412248.5:c.815C= ENSP00000412643.1:p.Thr272=
ENST00000437849.1:c.203C= ENSP00000391104.1:p.Thr68=
ENST00000463254.1:n.98C=
XM_005246449.1:c.815C= XP_005246506.1:p.Thr272=
XM_006712402.2:c.815C= XP_006712465.1:p.Thr272=
XM_011510929.1:c.815C= XP_011509231.1:p.Thr272=
XM_017003770.1:c.815C= XP_016859259.1:p.Thr272=
XR_002959253.1:n.1156C=