Canonical Allele Identifier: CA2669041648

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190405072-AGCCCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190405075_190405079del , CM000665.2:g.190405075_190405079del	GRCh38
NC_000003.11:g.190122864_190122868del , CM000665.1:g.190122864_190122868del	GRCh37
NC_000003.10:g.191605558_191605562del	NCBI36
NG_008149.1:g.22024_22028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.382+149_382+153del MANE Select	ENSP00000264734.3:n.382+149_382+153del
ENST00000456423.2:c.115-4828_115-4824del	ENSP00000414136.2:n.115-4828_115-4824del
ENST00000264734.2:c.592+149_592+153del	ENSP00000264734.2:n.592+149_592+153del
ENST00000456423.1:c.325-4828_325-4824del	ENSP00000414136.1:n.325-4828_325-4824del
NM_006580.3:c.592+149_592+153del	NP_006571.1:n.592+149_592+153del
NM_001378492.1:c.382+149_382+153del	NP_001365421.1:n.382+149_382+153del
NM_001378493.1:c.382+149_382+153del	NP_001365422.1:n.382+149_382+153del
NM_006580.4:c.382+149_382+153del MANE Select	NP_006571.2:n.382+149_382+153del