Canonical Allele Identifier: CA904279047

Gene: CLDN16

Linked Data

• dbSNP Id: rs1248163247
• gnomAD v3: 3-190388072-GC-G
• gnomAD v4: 3-190388072-GC-G
• MyVariant Identifiers: chr3:g.190105862del (hg19) ; chr3:g.190388073del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388075del , CM000665.2:g.190388075del	GRCh38
NC_000003.11:g.190105864del , CM000665.1:g.190105864del	GRCh37
NC_000003.10:g.191588558del	NCBI36
NG_008149.1:g.5024del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.2:c.-45del	ENSP00000264734.2:n.-45del
ENST00000468220.1:n.306+13472del
NM_006580.3:c.-45del	NP_006571.1:n.-45del
NM_001378492.1:c.-93-162del	NP_001365421.1:n.-93-162del
NM_001378493.1:c.-93-162del	NP_001365422.1:n.-93-162del