Canonical Allele Identifier: CA2669041584

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190404988-GGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404994_190404995del , CM000665.2:g.190404994_190404995del	GRCh38
NC_000003.11:g.190122783_190122784del , CM000665.1:g.190122783_190122784del	GRCh37
NC_000003.10:g.191605477_191605478del	NCBI36
NG_008149.1:g.21943_21944del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.382+68_382+69del MANE Select	ENSP00000264734.3:n.382+68_382+69del
ENST00000456423.2:c.115-4909_115-4908del	ENSP00000414136.2:n.115-4909_115-4908del
ENST00000264734.2:c.592+68_592+69del	ENSP00000264734.2:n.592+68_592+69del
ENST00000456423.1:c.325-4909_325-4908del	ENSP00000414136.1:n.325-4909_325-4908del
NM_006580.3:c.592+68_592+69del	NP_006571.1:n.592+68_592+69del
NM_001378492.1:c.382+68_382+69del	NP_001365421.1:n.382+68_382+69del
NM_001378493.1:c.382+68_382+69del	NP_001365422.1:n.382+68_382+69del
NM_006580.4:c.382+68_382+69del MANE Select	NP_006571.2:n.382+68_382+69del