Canonical Allele Identifier: CA1304746980
Gene: GALNT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165792360A= , CM000664.2:g.165792360A= GRCh38
NC_000002.11:g.166648870A= , CM000664.1:g.166648870A= GRCh37
NC_000002.10:g.166357116A= NCBI36
NG_012069.1:g.6934T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392701.8:c.-109+1655T= MANE Select ENSP00000376465.3:n.-109+1655T=
ENST00000392701.7:c.-109+1655T= ENSP00000376465.3:n.-109+1655T=
ENST00000412248.5:c.-228+1965T= ENSP00000412643.1:n.-228+1965T=
ENST00000414977.5:c.-228+1360T= ENSP00000413477.1:n.-228+1360T=
ENST00000422973.1:c.-228+1655T= ENSP00000413694.1:n.-228+1655T=
ENST00000431484.1:c.-109+2129T= ENSP00000397112.1:n.-109+2129T=
NM_004482.3:c.-109+1655T= NP_004473.2:n.-109+1655T=
XM_006712402.2:c.-109+1655T= XP_006712465.1:n.-109+1655T=
XM_011510929.1:c.-109+2129T= XP_011509231.1:n.-109+2129T=
XM_017003770.1:c.-109+1965T= XP_016859259.1:n.-109+1965T=
XR_002959253.1:n.233+1655T=
NM_004482.4:c.-109+1655T= MANE Select NP_004473.2:n.-109+1655T=