Canonical Allele Identifier: CA355766013
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.247A>T MANE Select ENSP00000264734.3:p.Ile83Phe
ENST00000456423.2:c.115-5112A>T ENSP00000414136.2:n.115-5112A>T
ENST00000264734.2:c.457A>T ENSP00000264734.2:p.Ile153Phe
ENST00000456423.1:c.325-5112A>T ENSP00000414136.1:n.325-5112A>T
ENST00000468220.1:n.439A>T
NM_006580.3:c.457A>T NP_006571.1:p.Ile153Phe
NM_001378492.1:c.247A>T NP_001365421.1:p.Ile83Phe
NM_001378493.1:c.247A>T NP_001365422.1:p.Ile83Phe
NM_006580.4:c.247A>T MANE Select NP_006571.2:p.Ile83Phe