Canonical Allele Identifier: CA648077149

Gene: CLDN16

Linked Data

• COSMIC: COSN21909317

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388094_190388095insA , CM000665.2:g.190388094_190388095insA	GRCh38
NC_000003.11:g.190105883_190105884insA , CM000665.1:g.190105883_190105884insA	GRCh37
NC_000003.10:g.191588577_191588578insA	NCBI36
NG_008149.1:g.5043_5044insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.2:c.-26_-25insA	ENSP00000264734.2:n.-26_-25insA
ENST00000468220.1:n.306+13491_306+13492insA
NM_006580.3:c.-26_-25insA	NP_006571.1:n.-26_-25insA
NM_001378492.1:c.-93-143_-93-142insA	NP_001365421.1:n.-93-143_-93-142insA
NM_001378493.1:c.-93-143_-93-142insA	NP_001365422.1:n.-93-143_-93-142insA