Canonical Allele Identifier: CA1304728082
Gene: GALNT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165747867T= , CM000664.2:g.165747867T= GRCh38
NC_000002.11:g.166604377T= , CM000664.1:g.166604377T= GRCh37
NC_000002.10:g.166312623T= NCBI36
NG_012069.1:g.51427A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392701.8:c.*914A= MANE Select ENSP00000376465.3:n.*914A=
ENST00000392701.7:c.*914A= ENSP00000376465.3:n.*914A=
ENST00000409882.5:c.*914A= ENSP00000386955.1:n.*914A=
NM_004482.3:c.*914A= NP_004473.2:n.*914A=
XM_005246449.1:c.*914A= XP_005246506.1:n.*914A=
XM_011510929.1:c.*914A= XP_011509231.1:n.*914A=
XM_017003770.1:c.*914A= XP_016859259.1:n.*914A=
NM_004482.4:c.*914A= MANE Select NP_004473.2:n.*914A=