Canonical Allele Identifier: CA648077145

Gene: CLDN16

Linked Data

• COSMIC: COSN17677212

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388070_190388071insG , CM000665.2:g.190388070_190388071insG	GRCh38
NC_000003.11:g.190105859_190105860insG , CM000665.1:g.190105859_190105860insG	GRCh37
NC_000003.10:g.191588553_191588554insG	NCBI36
NG_008149.1:g.5019_5020insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.2:c.-50_-49insG	ENSP00000264734.2:n.-50_-49insG
ENST00000468220.1:n.306+13467_306+13468insG
NM_006580.3:c.-50_-49insG	NP_006571.1:n.-50_-49insG
NM_001378492.1:c.-93-167_-93-166insG	NP_001365421.1:n.-93-167_-93-166insG
NM_001378493.1:c.-93-167_-93-166insG	NP_001365422.1:n.-93-167_-93-166insG