Canonical Allele Identifier: CA355762267
Gene: CLDN16 HGNC NCBI

Linked Data

gnomAD v4: 3-190388199-T-A
MyVariant Identifiers: chr3:g.190105988T>A (hg19) chr3:g.190388199T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388199T>A , CM000665.2:g.190388199T>A GRCh38
NC_000003.11:g.190105988T>A , CM000665.1:g.190105988T>A GRCh37
NC_000003.10:g.191588682T>A NCBI36
NG_008149.1:g.5148T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.-131T>A MANE Select ENSP00000264734.3:n.-131T>A
ENST00000456423.2:c.-131T>A ENSP00000414136.2:n.-131T>A
ENST00000264734.2:c.80T>A ENSP00000264734.2:p.Val27Glu
ENST00000456423.1:c.80T>A ENSP00000414136.1:p.Val27Glu
ENST00000468220.1:n.306+13596T>A
NM_006580.3:c.80T>A NP_006571.1:p.Val27Glu
NM_001378492.1:c.-93-38T>A NP_001365421.1:n.-93-38T>A
NM_001378493.1:c.-93-38T>A NP_001365422.1:n.-93-38T>A
NM_006580.4:c.-131T>A MANE Select NP_006571.2:n.-131T>A
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