Canonical Allele Identifier: CA1428775658

Gene: CLDN16

Linked Data

• dbSNP Id: rs1718553402

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388175del , CM000665.2:g.190388175del	GRCh38
NC_000003.11:g.190105964del , CM000665.1:g.190105964del	GRCh37
NC_000003.10:g.191588658del	NCBI36
NG_008149.1:g.5124del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.-155del MANE Select	ENSP00000264734.3:n.-155del
ENST00000456423.2:c.-155del	ENSP00000414136.2:n.-155del
ENST00000264734.2:c.56del	ENSP00000264734.2:p.Asn19ThrfsTer9
ENST00000456423.1:c.56del	ENSP00000414136.1:p.Asn19ThrfsTer9
ENST00000468220.1:n.306+13572del
NM_006580.3:c.56del	NP_006571.1:p.Asn19ThrfsTer9
NM_001378492.1:c.-93-62del	NP_001365421.1:n.-93-62del
NM_001378493.1:c.-93-62del	NP_001365422.1:n.-93-62del
NM_006580.4:c.-155del MANE Select	NP_006571.2:n.-155del