Canonical Allele Identifier: CA2759127790

Gene: KPNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160508485_160508489del , CM000665.2:g.160508485_160508489del	GRCh38
NC_000003.11:g.160226273_160226277del , CM000665.1:g.160226273_160226277del	GRCh37
NC_000003.10:g.161708967_161708971del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334256.9:c.1210-216_1210-212del MANE Select	ENSP00000334373.4:n.1210-216_1210-212del
ENST00000483437.2:c.1210-216_1210-212del	ENSP00000417172.2:n.1210-216_1210-212del
ENST00000676799.1:c.*1159-216_*1159-212del	ENSP00000503839.1:n.*1159-216_*1159-212del
ENST00000676866.1:c.1138-216_1138-212del	ENSP00000503291.1:n.1138-216_1138-212del
ENST00000676958.1:c.1322-216_1322-212del	ENSP00000503083.1:n.1322-216_1322-212del
ENST00000678020.1:n.1390-216_1390-212del
ENST00000678630.1:c.*1175-216_*1175-212del	ENSP00000504510.1:n.*1175-216_*1175-212del
ENST00000678765.1:c.1078-216_1078-212del	ENSP00000503064.1:n.1078-216_1078-212del
ENST00000334256.8:c.1210-216_1210-212del	ENSP00000334373.4:n.1210-216_1210-212del
ENST00000483437.1:c.253-216_253-212del	ENSP00000417172.1:n.253-216_253-212del
NM_002268.4:c.1210-216_1210-212del	NP_002259.1:n.1210-216_1210-212del
NM_002268.5:c.1210-216_1210-212del MANE Select	NP_002259.1:n.1210-216_1210-212del