Canonical Allele Identifier: CA2512887584

Gene: KPNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160508541_160508598del , CM000665.2:g.160508541_160508598del	GRCh38
NC_000003.11:g.160226329_160226386del , CM000665.1:g.160226329_160226386del	GRCh37
NC_000003.10:g.161709023_161709080del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000334256.9:c.1210-329_1210-272del MANE Select	ENSP00000334373.4:n.1210-329_1210-272del
ENST00000483437.2:c.1210-329_1210-272del	ENSP00000417172.2:n.1210-329_1210-272del
ENST00000676799.1:c.*1159-329_*1159-272del	ENSP00000503839.1:n.*1159-329_*1159-272de...
ENST00000676866.1:c.1138-329_1138-272del	ENSP00000503291.1:n.1138-329_1138-272del
ENST00000676958.1:c.1322-329_1322-272del	ENSP00000503083.1:n.1322-329_1322-272del
ENST00000678020.1:n.1390-329_1390-272del
ENST00000678630.1:c.*1175-329_*1175-272del	ENSP00000504510.1:n.*1175-329_*1175-272de...
ENST00000678765.1:c.1078-329_1078-272del	ENSP00000503064.1:n.1078-329_1078-272del
ENST00000334256.8:c.1210-329_1210-272del	ENSP00000334373.4:n.1210-329_1210-272del
ENST00000483437.1:c.253-329_253-272del	ENSP00000417172.1:n.253-329_253-272del
NM_002268.4:c.1210-329_1210-272del	NP_002259.1:n.1210-329_1210-272del
NM_002268.5:c.1210-329_1210-272del MANE Select	NP_002259.1:n.1210-329_1210-272del