Canonical Allele Identifier: CA355762152

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190105936A>C (hg19) ; chr3:g.190388147A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388147A>C , CM000665.2:g.190388147A>C	GRCh38
NC_000003.11:g.190105936A>C , CM000665.1:g.190105936A>C	GRCh37
NC_000003.10:g.191588630A>C	NCBI36
NG_008149.1:g.5096A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-183A>C	ENSP00000414136.2:n.-183A>C
ENST00000264734.2:c.28A>C	ENSP00000264734.2:p.Thr10Pro
ENST00000456423.1:c.28A>C	ENSP00000414136.1:p.Thr10Pro
ENST00000468220.1:n.306+13544A>C
NM_006580.3:c.28A>C	NP_006571.1:p.Thr10Pro
NM_001378492.1:c.-93-90A>C	NP_001365421.1:n.-93-90A>C
NM_001378493.1:c.-93-90A>C	NP_001365422.1:n.-93-90A>C