Canonical Allele Identifier: CA355767142
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408421T>A , CM000665.2:g.190408421T>A GRCh38
NC_000003.11:g.190126210T>A , CM000665.1:g.190126210T>A GRCh37
NC_000003.10:g.191608904T>A NCBI36
NG_008149.1:g.25370T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.490T>A MANE Select ENSP00000264734.3:p.Trp164Arg
ENST00000456423.2:c.115-1482T>A ENSP00000414136.2:n.115-1482T>A
ENST00000264734.2:c.700T>A ENSP00000264734.2:p.Trp234Arg
ENST00000456423.1:c.325-1482T>A ENSP00000414136.1:n.325-1482T>A
NM_006580.3:c.700T>A NP_006571.1:p.Trp234Arg
NM_001378492.1:c.490T>A NP_001365421.1:p.Trp164Arg
NM_001378493.1:c.490T>A NP_001365422.1:p.Trp164Arg
NM_006580.4:c.490T>A MANE Select NP_006571.2:p.Trp164Arg