Canonical Allele Identifier: CA2669040786

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190402281-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402281G>A , CM000665.2:g.190402281G>A	GRCh38
NC_000003.11:g.190120070G>A , CM000665.1:g.190120070G>A	GRCh37
NC_000003.10:g.191602764G>A	NCBI36
NG_008149.1:g.19230G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-56G>A MANE Select	ENSP00000264734.3:n.115-56G>A
ENST00000456423.2:c.115-7622G>A	ENSP00000414136.2:n.115-7622G>A
ENST00000264734.2:c.325-56G>A	ENSP00000264734.2:n.325-56G>A
ENST00000456423.1:c.325-7622G>A	ENSP00000414136.1:n.325-7622G>A
ENST00000468220.1:n.307-56G>A
NM_006580.3:c.325-56G>A	NP_006571.1:n.325-56G>A
NM_001378492.1:c.115-56G>A	NP_001365421.1:n.115-56G>A
NM_001378493.1:c.115-56G>A	NP_001365422.1:n.115-56G>A
NM_006580.4:c.115-56G>A MANE Select	NP_006571.2:n.115-56G>A