Canonical Allele Identifier: CA760162638
Gene: GALNT3 HGNC NCBI

Linked Data

dbSNP Id: rs1339218761
gnomAD v3: 2-165747859-CT-C
gnomAD v4: 2-165747859-CT-C
MyVariant Identifiers: chr2:g.166604370del (hg19) chr2:g.165747860del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165747864del , CM000664.2:g.165747864del GRCh38
NC_000002.11:g.166604374del , CM000664.1:g.166604374del GRCh37
NC_000002.10:g.166312620del NCBI36
NG_012069.1:g.51434del

Transcript Alleles

HGVS Amino-acid Change
ENST00000392701.8:c.*921del MANE Select ENSP00000376465.3:n.*921del
ENST00000392701.7:c.*921del ENSP00000376465.3:n.*921del
ENST00000409882.5:c.*921del ENSP00000386955.1:n.*921del
NM_004482.3:c.*921del NP_004473.2:n.*921del
XM_005246449.1:c.*921del XP_005246506.1:n.*921del
XM_011510929.1:c.*921del XP_011509231.1:n.*921del
XM_017003770.1:c.*921del XP_016859259.1:n.*921del
NM_004482.4:c.*921del MANE Select NP_004473.2:n.*921del
Search 100 bp 5'
Search 100 bp 3'