Canonical Allele Identifier: CA891862916

Gene: CLDN16

Linked Data

• ClinVar Variation Id: 591491
• ClinVar RCV Id: RCV000722670
• dbSNP Id: rs1560093684

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388187_190388189del , CM000665.2:g.190388187_190388189del	GRCh38
NC_000003.11:g.190105976_190105978del , CM000665.1:g.190105976_190105978del	GRCh37
NC_000003.10:g.191588670_191588672del	NCBI36
NG_008149.1:g.5136_5138del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.-143_-141del MANE Select	ENSP00000264734.3:n.-143_-141del
ENST00000456423.2:c.-143_-141del	ENSP00000414136.2:n.-143_-141del
ENST00000264734.2:c.68_70del	ENSP00000264734.2:p.Leu23del
ENST00000456423.1:c.68_70del	ENSP00000414136.1:p.Leu23del
ENST00000468220.1:n.306+13584_306+13586del
NM_006580.3:c.68_70del	NP_006571.1:p.Leu23del
NM_001378492.1:c.-93-50_-93-48del	NP_001365421.1:n.-93-50_-93-48del
NM_001378493.1:c.-93-50_-93-48del	NP_001365422.1:n.-93-50_-93-48del
NM_006580.4:c.-143_-141del MANE Select	NP_006571.2:n.-143_-141del