Canonical Allele Identifier: CA1428759346
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404791A= , CM000665.2:g.190404791A= GRCh38
NC_000003.11:g.190122580A= , CM000665.1:g.190122580A= GRCh37
NC_000003.10:g.191605274A= NCBI36
NG_008149.1:g.21740A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.247A= MANE Select ENSP00000264734.3:p.Ile83=
ENST00000456423.2:c.115-5112A= ENSP00000414136.2:n.115-5112A=
ENST00000264734.2:c.457A= ENSP00000264734.2:p.Ile153=
ENST00000456423.1:c.325-5112A= ENSP00000414136.1:n.325-5112A=
ENST00000468220.1:n.439A=
NM_006580.3:c.457A= NP_006571.1:p.Ile153=
NM_001378492.1:c.247A= NP_001365421.1:p.Ile83=
NM_001378493.1:c.247A= NP_001365422.1:p.Ile83=
NM_006580.4:c.247A= MANE Select NP_006571.2:p.Ile83=