Canonical Allele Identifier: CA355766941
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.397A>G MANE Select ENSP00000264734.3:p.Ile133Val
ENST00000456423.2:c.115-1575A>G ENSP00000414136.2:n.115-1575A>G
ENST00000264734.2:c.607A>G ENSP00000264734.2:p.Ile203Val
ENST00000456423.1:c.325-1575A>G ENSP00000414136.1:n.325-1575A>G
NM_006580.3:c.607A>G NP_006571.1:p.Ile203Val
NM_001378492.1:c.397A>G NP_001365421.1:p.Ile133Val
NM_001378493.1:c.397A>G NP_001365422.1:p.Ile133Val
NM_006580.4:c.397A>G MANE Select NP_006571.2:p.Ile133Val