Canonical Allele Identifier: CA2669041589

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190404993-GAGTTGTGCTGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404996_190405006del , CM000665.2:g.190404996_190405006del	GRCh38
NC_000003.11:g.190122785_190122795del , CM000665.1:g.190122785_190122795del	GRCh37
NC_000003.10:g.191605479_191605489del	NCBI36
NG_008149.1:g.21945_21955del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.382+70_382+80del MANE Select	ENSP00000264734.3:n.382+70_382+80del
ENST00000456423.2:c.115-4907_115-4897del	ENSP00000414136.2:n.115-4907_115-4897del
ENST00000264734.2:c.592+70_592+80del	ENSP00000264734.2:n.592+70_592+80del
ENST00000456423.1:c.325-4907_325-4897del	ENSP00000414136.1:n.325-4907_325-4897del
NM_006580.3:c.592+70_592+80del	NP_006571.1:n.592+70_592+80del
NM_001378492.1:c.382+70_382+80del	NP_001365421.1:n.382+70_382+80del
NM_001378493.1:c.382+70_382+80del	NP_001365422.1:n.382+70_382+80del
NM_006580.4:c.382+70_382+80del MANE Select	NP_006571.2:n.382+70_382+80del