Canonical Allele Identifier: CA355762588

Gene: CLDN16

Linked Data

• dbSNP Id: rs965435011
• gnomAD v3: 3-190388354-G-C
• gnomAD v4: 3-190388354-G-C
• MyVariant Identifiers: chr3:g.190106143G>C (hg19) ; chr3:g.190388354G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388354G>C , CM000665.2:g.190388354G>C	GRCh38
NC_000003.11:g.190106143G>C , CM000665.1:g.190106143G>C	GRCh37
NC_000003.10:g.191588837G>C	NCBI36
NG_008149.1:g.5303G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264734.3:c.25G>C MANE Select	ENSP00000264734.3:p.Ala9Pro
ENST00000456423.2:c.25G>C	ENSP00000414136.2:p.Ala9Pro
ENST00000264734.2:c.235G>C	ENSP00000264734.2:p.Ala79Pro
ENST00000456423.1:c.235G>C	ENSP00000414136.1:p.Ala79Pro
ENST00000468220.1:n.306+13751G>C
NM_006580.3:c.235G>C	NP_006571.1:p.Ala79Pro
NM_001378492.1:c.25G>C	NP_001365421.1:p.Ala9Pro
NM_001378493.1:c.25G>C	NP_001365422.1:p.Ala9Pro
NM_006580.4:c.25G>C MANE Select	NP_006571.2:p.Ala9Pro