Canonical Allele Identifier: CA1428762759

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190408397_190408398delinsCT , CM000665.2:g.190408397_190408398delinsCT	GRCh38
NC_000003.11:g.190126186_190126187delinsCT , CM000665.1:g.190126186_190126187delinsCT	GRCh37
NC_000003.10:g.191608880_191608881delinsCT	NCBI36
NG_008149.1:g.25346_25347delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.466_467delinsCT MANE Select	ENSP00000264734.3:p.Leu156=
ENST00000456423.2:c.115-1506_115-1505delinsCT	ENSP00000414136.2:n.115-1506_115-1505delinsCT
ENST00000264734.2:c.676_677delinsCT	ENSP00000264734.2:p.Leu226=
ENST00000456423.1:c.325-1506_325-1505delinsCT	ENSP00000414136.1:n.325-1506_325-1505delinsCT
NM_006580.3:c.676_677delinsCT	NP_006571.1:p.Leu226=
NM_001378492.1:c.466_467delinsCT	NP_001365421.1:p.Leu156=
NM_001378493.1:c.466_467delinsCT	NP_001365422.1:p.Leu156=
NM_006580.4:c.466_467delinsCT MANE Select	NP_006571.2:p.Leu156=