Canonical Allele Identifier: CA2577990755

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190402419-CCAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402420_190402422del , CM000665.2:g.190402420_190402422del	GRCh38
NC_000003.11:g.190120209_190120211del , CM000665.1:g.190120209_190120211del	GRCh37
NC_000003.10:g.191602903_191602905del	NCBI36
NG_008149.1:g.19369_19371del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.198_200del MANE Select	ENSP00000264734.3:p.Ile67del
ENST00000456423.2:c.115-7483_115-7481del	ENSP00000414136.2:n.115-7483_115-7481del
ENST00000264734.2:c.408_410del	ENSP00000264734.2:p.Ile137del
ENST00000456423.1:c.325-7483_325-7481del	ENSP00000414136.1:n.325-7483_325-7481del
ENST00000468220.1:n.390_392del
NM_006580.3:c.408_410del	NP_006571.1:p.Ile137del
NM_001378492.1:c.198_200del	NP_001365421.1:p.Ile67del
NM_001378493.1:c.198_200del	NP_001365422.1:p.Ile67del
NM_006580.4:c.198_200del MANE Select	NP_006571.2:p.Ile67del