Canonical Allele Identifier: CA355762521
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388322T>A , CM000665.2:g.190388322T>A GRCh38
NC_000003.11:g.190106111T>A , CM000665.1:g.190106111T>A GRCh37
NC_000003.10:g.191588805T>A NCBI36
NG_008149.1:g.5271T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.-8T>A MANE Select ENSP00000264734.3:n.-8T>A
ENST00000456423.2:c.-8T>A ENSP00000414136.2:n.-8T>A
ENST00000264734.2:c.203T>A ENSP00000264734.2:p.Leu68His
ENST00000456423.1:c.203T>A ENSP00000414136.1:p.Leu68His
ENST00000468220.1:n.306+13719T>A
NM_006580.3:c.203T>A NP_006571.1:p.Leu68His
NM_001378492.1:c.-8T>A NP_001365421.1:n.-8T>A
NM_001378493.1:c.-8T>A NP_001365422.1:n.-8T>A
NM_006580.4:c.-8T>A MANE Select NP_006571.2:n.-8T>A