Canonical Allele Identifier: CA2661746026

Gene: GALNT3

Linked Data

• gnomAD v4: 2-165747905-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165747905T>C , CM000664.2:g.165747905T>C	GRCh38
NC_000002.11:g.166604415T>C , CM000664.1:g.166604415T>C	GRCh37
NC_000002.10:g.166312661T>C	NCBI36
NG_012069.1:g.51389A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392701.8:c.*876A>G MANE Select	ENSP00000376465.3:n.*876A>G
ENST00000392701.7:c.*876A>G	ENSP00000376465.3:n.*876A>G
ENST00000409882.5:c.*876A>G	ENSP00000386955.1:n.*876A>G
NM_004482.3:c.*876A>G	NP_004473.2:n.*876A>G
XM_005246449.1:c.*876A>G	XP_005246506.1:n.*876A>G
XM_011510929.1:c.*876A>G	XP_011509231.1:n.*876A>G
XM_017003770.1:c.*876A>G	XP_016859259.1:n.*876A>G
NM_004482.4:c.*876A>G MANE Select	NP_004473.2:n.*876A>G