Canonical Allele Identifier: CA904287184

Gene: CLDN16

Linked Data

• dbSNP Id: rs1268468646
• gnomAD v3: 3-190402248-AAC-A
• gnomAD v4: 3-190402248-AAC-A
• MyVariant Identifiers: chr3:g.190120038_190120039del (hg19) ; chr3:g.190402249_190402250del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402252_190402253del , CM000665.2:g.190402252_190402253del	GRCh38
NC_000003.11:g.190120041_190120042del , CM000665.1:g.190120041_190120042del	GRCh37
NC_000003.10:g.191602735_191602736del	NCBI36
NG_008149.1:g.19201_19202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-85_115-84del MANE Select	ENSP00000264734.3:n.115-85_115-84del
ENST00000456423.2:c.115-7651_115-7650del	ENSP00000414136.2:n.115-7651_115-7650del
ENST00000264734.2:c.325-85_325-84del	ENSP00000264734.2:n.325-85_325-84del
ENST00000456423.1:c.325-7651_325-7650del	ENSP00000414136.1:n.325-7651_325-7650del
ENST00000468220.1:n.307-85_307-84del
NM_006580.3:c.325-85_325-84del	NP_006571.1:n.325-85_325-84del
NM_001378492.1:c.115-85_115-84del	NP_001365421.1:n.115-85_115-84del
NM_001378493.1:c.115-85_115-84del	NP_001365422.1:n.115-85_115-84del
NM_006580.4:c.115-85_115-84del MANE Select	NP_006571.2:n.115-85_115-84del