Canonical Allele Identifier: CA1304728101
Gene: GALNT3 HGNC NCBI

Linked Data

dbSNP Id: rs1688287401

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165747883C>A , CM000664.2:g.165747883C>A GRCh38
NC_000002.11:g.166604393C>A , CM000664.1:g.166604393C>A GRCh37
NC_000002.10:g.166312639C>A NCBI36
NG_012069.1:g.51411G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392701.8:c.*898G>T MANE Select ENSP00000376465.3:n.*898G>T
ENST00000392701.7:c.*898G>T ENSP00000376465.3:n.*898G>T
ENST00000409882.5:c.*898G>T ENSP00000386955.1:n.*898G>T
NM_004482.3:c.*898G>T NP_004473.2:n.*898G>T
XM_005246449.1:c.*898G>T XP_005246506.1:n.*898G>T
XM_011510929.1:c.*898G>T XP_011509231.1:n.*898G>T
XM_017003770.1:c.*898G>T XP_016859259.1:n.*898G>T
NM_004482.4:c.*898G>T MANE Select NP_004473.2:n.*898G>T