Canonical Allele Identifier: CA355766942
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408328A>T , CM000665.2:g.190408328A>T GRCh38
NC_000003.11:g.190126117A>T , CM000665.1:g.190126117A>T GRCh37
NC_000003.10:g.191608811A>T NCBI36
NG_008149.1:g.25277A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.397A>T MANE Select ENSP00000264734.3:p.Ile133Phe
ENST00000456423.2:c.115-1575A>T ENSP00000414136.2:n.115-1575A>T
ENST00000264734.2:c.607A>T ENSP00000264734.2:p.Ile203Phe
ENST00000456423.1:c.325-1575A>T ENSP00000414136.1:n.325-1575A>T
NM_006580.3:c.607A>T NP_006571.1:p.Ile203Phe
NM_001378492.1:c.397A>T NP_001365421.1:p.Ile133Phe
NM_001378493.1:c.397A>T NP_001365422.1:p.Ile133Phe
NM_006580.4:c.397A>T MANE Select NP_006571.2:p.Ile133Phe