Canonical Allele Identifier: CA2669041625

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190405048-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190405053dup , CM000665.2:g.190405053dup	GRCh38
NC_000003.11:g.190122842dup , CM000665.1:g.190122842dup	GRCh37
NC_000003.10:g.191605536dup	NCBI36
NG_008149.1:g.22002dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.382+127dup MANE Select	ENSP00000264734.3:n.382+127dup
ENST00000456423.2:c.115-4850dup	ENSP00000414136.2:n.115-4850dup
ENST00000264734.2:c.592+127dup	ENSP00000264734.2:n.592+127dup
ENST00000456423.1:c.325-4850dup	ENSP00000414136.1:n.325-4850dup
NM_006580.3:c.592+127dup	NP_006571.1:n.592+127dup
NM_001378492.1:c.382+127dup	NP_001365421.1:n.382+127dup
NM_001378493.1:c.382+127dup	NP_001365422.1:n.382+127dup
NM_006580.4:c.382+127dup MANE Select	NP_006571.2:n.382+127dup