Canonical Allele Identifier: CA2570597450

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404538_190404539insTAAT , CM000665.2:g.190404538_190404539insTAAT	GRCh38
NC_000003.11:g.190122327_190122328insTAAT , CM000665.1:g.190122327_190122328insTAAT	GRCh37
NC_000003.10:g.191605021_191605022insTAAT	NCBI36
NG_008149.1:g.21487_21488insTAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.218-224_218-223insTAAT MANE Select	ENSP00000264734.3:n.218-224_218-223insTAAT
ENST00000456423.2:c.115-5365_115-5364insTAAT	ENSP00000414136.2:n.115-5365_115-5364insTAAT
ENST00000264734.2:c.428-224_428-223insTAAT	ENSP00000264734.2:n.428-224_428-223insTAAT
ENST00000456423.1:c.325-5365_325-5364insTAAT	ENSP00000414136.1:n.325-5365_325-5364insTAAT
ENST00000468220.1:n.410-224_410-223insTAAT
NM_006580.3:c.428-224_428-223insTAAT	NP_006571.1:n.428-224_428-223insTAAT
NM_001378492.1:c.218-224_218-223insTAAT	NP_001365421.1:n.218-224_218-223insTAAT
NM_001378493.1:c.218-224_218-223insTAAT	NP_001365422.1:n.218-224_218-223insTAAT
NM_006580.4:c.218-224_218-223insTAAT MANE Select	NP_006571.2:n.218-224_218-223insTAAT