Canonical Allele Identifier: CA355762137

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190388139-T-C
• MyVariant Identifiers: chr3:g.190105928T>C (hg19) ; chr3:g.190388139T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388139T>C , CM000665.2:g.190388139T>C	GRCh38
NC_000003.11:g.190105928T>C , CM000665.1:g.190105928T>C	GRCh37
NC_000003.10:g.191588622T>C	NCBI36
NG_008149.1:g.5088T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-191T>C	ENSP00000414136.2:n.-191T>C
ENST00000264734.2:c.20T>C	ENSP00000264734.2:p.Leu7Pro
ENST00000456423.1:c.20T>C	ENSP00000414136.1:p.Leu7Pro
ENST00000468220.1:n.306+13536T>C
NM_006580.3:c.20T>C	NP_006571.1:p.Leu7Pro
NM_001378492.1:c.-93-98T>C	NP_001365421.1:n.-93-98T>C
NM_001378493.1:c.-93-98T>C	NP_001365422.1:n.-93-98T>C