Canonical Allele Identifier: CA1428775625

Gene: CLDN16

Linked Data

• dbSNP Id: rs1718552903
• gnomAD v4: 3-190388158-GTAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388163_190388165del , CM000665.2:g.190388163_190388165del	GRCh38
NC_000003.11:g.190105952_190105954del , CM000665.1:g.190105952_190105954del	GRCh37
NC_000003.10:g.191588646_191588648del	NCBI36
NG_008149.1:g.5112_5114del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-167_-165del	ENSP00000414136.2:n.-167_-165del
ENST00000264734.2:c.44_46del	ENSP00000264734.2:p.Tyr15del
ENST00000456423.1:c.44_46del	ENSP00000414136.1:p.Tyr15del
ENST00000468220.1:n.306+13560_306+13562del
NM_006580.3:c.44_46del	NP_006571.1:p.Tyr15del
NM_001378492.1:c.-93-74_-93-72del	NP_001365421.1:n.-93-74_-93-72del
NM_001378493.1:c.-93-74_-93-72del	NP_001365422.1:n.-93-74_-93-72del