Canonical Allele Identifier: CA2669041564

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190404820-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404823del , CM000665.2:g.190404823del	GRCh38
NC_000003.11:g.190122612del , CM000665.1:g.190122612del	GRCh37
NC_000003.10:g.191605306del	NCBI36
NG_008149.1:g.21772del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.279del MANE Select	ENSP00000264734.3:p.Leu94SerfsTer10
ENST00000456423.2:c.115-5080del	ENSP00000414136.2:n.115-5080del
ENST00000264734.2:c.489del	ENSP00000264734.2:p.Leu164SerfsTer10
ENST00000456423.1:c.325-5080del	ENSP00000414136.1:n.325-5080del
ENST00000468220.1:n.471del
NM_006580.3:c.489del	NP_006571.1:p.Leu164SerfsTer10
NM_001378492.1:c.279del	NP_001365421.1:p.Leu94SerfsTer10
NM_001378493.1:c.279del	NP_001365422.1:p.Leu94SerfsTer10
NM_006580.4:c.279del MANE Select	NP_006571.2:p.Leu94SerfsTer10