Canonical Allele Identifier: CA2518992808

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402666_190402670del , CM000665.2:g.190402666_190402670del	GRCh38
NC_000003.11:g.190120455_190120459del , CM000665.1:g.190120455_190120459del	GRCh37
NC_000003.10:g.191603149_191603153del	NCBI36
NG_008149.1:g.19615_19619del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.217+227_217+231del MANE Select	ENSP00000264734.3:n.217+227_217+231del
ENST00000456423.2:c.115-7237_115-7233del	ENSP00000414136.2:n.115-7237_115-7233del
ENST00000264734.2:c.427+227_427+231del	ENSP00000264734.2:n.427+227_427+231del
ENST00000456423.1:c.325-7237_325-7233del	ENSP00000414136.1:n.325-7237_325-7233del
ENST00000468220.1:n.409+227_409+231del
NM_006580.3:c.427+227_427+231del	NP_006571.1:n.427+227_427+231del
NM_001378492.1:c.217+227_217+231del	NP_001365421.1:n.217+227_217+231del
NM_001378493.1:c.217+227_217+231del	NP_001365422.1:n.217+227_217+231del
NM_006580.4:c.217+227_217+231del MANE Select	NP_006571.2:n.217+227_217+231del