Canonical Allele Identifier: CA1428775623

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388158_190388161delinsGTAT , CM000665.2:g.190388158_190388161delinsGTAT	GRCh38
NC_000003.11:g.190105947_190105950delinsGTAT , CM000665.1:g.190105947_190105950delinsGTAT	GRCh37
NC_000003.10:g.191588641_191588644delinsGTAT	NCBI36
NG_008149.1:g.5107_5110delinsGTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-172_-169delinsGTAT	ENSP00000414136.2:n.-172_-169delinsGTAT
ENST00000264734.2:c.39_42delinsGTAT	ENSP00000264734.2:p.Leu13=
ENST00000456423.1:c.39_42delinsGTAT	ENSP00000414136.1:p.Leu13=
ENST00000468220.1:n.306+13555_306+13558delinsGTAT
NM_006580.3:c.39_42delinsGTAT	NP_006571.1:p.Leu13=
NM_001378492.1:c.-93-79_-93-76delinsGTAT	NP_001365421.1:n.-93-79_-93-76delinsGTAT
NM_001378493.1:c.-93-79_-93-76delinsGTAT	NP_001365422.1:n.-93-79_-93-76delinsGTAT