Canonical Allele Identifier: CA2669041733

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190408426-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190408427del , CM000665.2:g.190408427del	GRCh38
NC_000003.11:g.190126216del , CM000665.1:g.190126216del	GRCh37
NC_000003.10:g.191608910del	NCBI36
NG_008149.1:g.25376del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.496del MANE Select	ENSP00000264734.3:p.Cys166ValfsTer?
ENST00000456423.2:c.115-1476del	ENSP00000414136.2:n.115-1476del
ENST00000264734.2:c.706del	ENSP00000264734.2:p.Cys236ValfsTer?
ENST00000456423.1:c.325-1476del	ENSP00000414136.1:n.325-1476del
NM_006580.3:c.706del	NP_006571.1:p.Cys236ValfsTer?
NM_001378492.1:c.496del	NP_001365421.1:p.Cys166ValfsTer?
NM_001378493.1:c.496del	NP_001365422.1:p.Cys166ValfsTer?
NM_006580.4:c.496del MANE Select	NP_006571.2:p.Cys166ValfsTer?