Canonical Allele Identifier: CA355762135

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190105927C>G (hg19) ; chr3:g.190388138C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388138C>G , CM000665.2:g.190388138C>G	GRCh38
NC_000003.11:g.190105927C>G , CM000665.1:g.190105927C>G	GRCh37
NC_000003.10:g.191588621C>G	NCBI36
NG_008149.1:g.5087C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-192C>G	ENSP00000414136.2:n.-192C>G
ENST00000264734.2:c.19C>G	ENSP00000264734.2:p.Leu7Val
ENST00000456423.1:c.19C>G	ENSP00000414136.1:p.Leu7Val
ENST00000468220.1:n.306+13535C>G
NM_006580.3:c.19C>G	NP_006571.1:p.Leu7Val
NM_001378492.1:c.-93-99C>G	NP_001365421.1:n.-93-99C>G
NM_001378493.1:c.-93-99C>G	NP_001365422.1:n.-93-99C>G