Canonical Allele Identifier: CA904287079

Gene: CLDN16

Linked Data

• dbSNP Id: rs542542114
• gnomAD v3: 3-190402076-A-C
• gnomAD v4: 3-190402076-A-C
• MyVariant Identifiers: chr3:g.190119865A>C (hg19) ; chr3:g.190402076A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402076A>C , CM000665.2:g.190402076A>C	GRCh38
NC_000003.11:g.190119865A>C , CM000665.1:g.190119865A>C	GRCh37
NC_000003.10:g.191602559A>C	NCBI36
NG_008149.1:g.19025A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-261A>C MANE Select	ENSP00000264734.3:n.115-261A>C
ENST00000456423.2:c.115-7827A>C	ENSP00000414136.2:n.115-7827A>C
ENST00000264734.2:c.325-261A>C	ENSP00000264734.2:n.325-261A>C
ENST00000456423.1:c.325-7827A>C	ENSP00000414136.1:n.325-7827A>C
ENST00000468220.1:n.307-261A>C
NM_006580.3:c.325-261A>C	NP_006571.1:n.325-261A>C
NM_001378492.1:c.115-261A>C	NP_001365421.1:n.115-261A>C
NM_001378493.1:c.115-261A>C	NP_001365422.1:n.115-261A>C
NM_006580.4:c.115-261A>C MANE Select	NP_006571.2:n.115-261A>C