Canonical Allele Identifier: CA904278978

Gene: CLDN16

Linked Data

• dbSNP Id: rs1220410147
• gnomAD v3: 3-190387968-TC-T
• gnomAD v4: 3-190387968-TC-T
• MyVariant Identifiers: chr3:g.190105758del (hg19) ; chr3:g.190387969del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190387973del , CM000665.2:g.190387973del	GRCh38
NC_000003.11:g.190105762del , CM000665.1:g.190105762del	GRCh37
NC_000003.10:g.191588456del	NCBI36
NG_008149.1:g.4922del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.2:c.-147del	ENSP00000264734.2:n.-147del
ENST00000468220.1:n.306+13370del
NM_006580.3:c.-147del	NP_006571.1:n.-147del
NM_001378492.1:c.-93-264del	NP_001365421.1:n.-93-264del
NM_001378493.1:c.-93-264del	NP_001365422.1:n.-93-264del