Canonical Allele Identifier: CA355762377
Gene: CLDN16 HGNC NCBI

Linked Data

gnomAD v4: 3-190388250-A-G
MyVariant Identifiers: chr3:g.190106039A>G (hg19) chr3:g.190388250A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388250A>G , CM000665.2:g.190388250A>G GRCh38
NC_000003.11:g.190106039A>G , CM000665.1:g.190106039A>G GRCh37
NC_000003.10:g.191588733A>G NCBI36
NG_008149.1:g.5199A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.-80A>G MANE Select ENSP00000264734.3:n.-80A>G
ENST00000456423.2:c.-80A>G ENSP00000414136.2:n.-80A>G
ENST00000264734.2:c.131A>G ENSP00000264734.2:p.Gln44Arg
ENST00000456423.1:c.131A>G ENSP00000414136.1:p.Gln44Arg
ENST00000468220.1:n.306+13647A>G
NM_006580.3:c.131A>G NP_006571.1:p.Gln44Arg
NM_001378492.1:c.-80A>G NP_001365421.1:n.-80A>G
NM_001378493.1:c.-80A>G NP_001365422.1:n.-80A>G
NM_006580.4:c.-80A>G MANE Select NP_006571.2:n.-80A>G
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