Canonical Allele Identifier: CA1428758866

Gene: CLDN16

Linked Data

• dbSNP Id: rs1719035783

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404351del , CM000665.2:g.190404351del	GRCh38
NC_000003.11:g.190122140del , CM000665.1:g.190122140del	GRCh37
NC_000003.10:g.191604834del	NCBI36
NG_008149.1:g.21300del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.218-411del MANE Select	ENSP00000264734.3:n.218-411del
ENST00000456423.2:c.115-5552del	ENSP00000414136.2:n.115-5552del
ENST00000264734.2:c.428-411del	ENSP00000264734.2:n.428-411del
ENST00000456423.1:c.325-5552del	ENSP00000414136.1:n.325-5552del
ENST00000468220.1:n.410-411del
NM_006580.3:c.428-411del	NP_006571.1:n.428-411del
NM_001378492.1:c.218-411del	NP_001365421.1:n.218-411del
NM_001378493.1:c.218-411del	NP_001365422.1:n.218-411del
NM_006580.4:c.218-411del MANE Select	NP_006571.2:n.218-411del