Canonical Allele Identifier: CA2669041645

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190405069-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190405071del , CM000665.2:g.190405071del	GRCh38
NC_000003.11:g.190122860del , CM000665.1:g.190122860del	GRCh37
NC_000003.10:g.191605554del	NCBI36
NG_008149.1:g.22020del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.382+145del MANE Select	ENSP00000264734.3:n.382+145del
ENST00000456423.2:c.115-4832del	ENSP00000414136.2:n.115-4832del
ENST00000264734.2:c.592+145del	ENSP00000264734.2:n.592+145del
ENST00000456423.1:c.325-4832del	ENSP00000414136.1:n.325-4832del
NM_006580.3:c.592+145del	NP_006571.1:n.592+145del
NM_001378492.1:c.382+145del	NP_001365421.1:n.382+145del
NM_001378493.1:c.382+145del	NP_001365422.1:n.382+145del
NM_006580.4:c.382+145del MANE Select	NP_006571.2:n.382+145del