Canonical Allele Identifier: CA355762124

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190105921A>T (hg19) ; chr3:g.190388132A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388132A>T , CM000665.2:g.190388132A>T	GRCh38
NC_000003.11:g.190105921A>T , CM000665.1:g.190105921A>T	GRCh37
NC_000003.10:g.191588615A>T	NCBI36
NG_008149.1:g.5081A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-198A>T	ENSP00000414136.2:n.-198A>T
ENST00000264734.2:c.13A>T	ENSP00000264734.2:p.Thr5Ser
ENST00000456423.1:c.13A>T	ENSP00000414136.1:p.Thr5Ser
ENST00000468220.1:n.306+13529A>T
NM_006580.3:c.13A>T	NP_006571.1:p.Thr5Ser
NM_001378492.1:c.-93-105A>T	NP_001365421.1:n.-93-105A>T
NM_001378493.1:c.-93-105A>T	NP_001365422.1:n.-93-105A>T