Canonical Allele Identifier: CA1415222423

Gene: KPNA4

Linked Data

• dbSNP Id: rs1721029340

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160508477_160508478del , CM000665.2:g.160508477_160508478del	GRCh38
NC_000003.11:g.160226265_160226266del , CM000665.1:g.160226265_160226266del	GRCh37
NC_000003.10:g.161708959_161708960del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000334256.9:c.1210-208_1210-207del MANE Select	ENSP00000334373.4:n.1210-208_1210-207del
ENST00000483437.2:c.1210-208_1210-207del	ENSP00000417172.2:n.1210-208_1210-207del
ENST00000676799.1:c.*1159-208_*1159-207del	ENSP00000503839.1:n.*1159-208_*1159-207del
ENST00000676866.1:c.1138-208_1138-207del	ENSP00000503291.1:n.1138-208_1138-207del
ENST00000676958.1:c.1322-208_1322-207del	ENSP00000503083.1:n.1322-208_1322-207del
ENST00000678020.1:n.1390-208_1390-207del
ENST00000678630.1:c.*1175-208_*1175-207del	ENSP00000504510.1:n.*1175-208_*1175-207del
ENST00000678765.1:c.1078-208_1078-207del	ENSP00000503064.1:n.1078-208_1078-207del
ENST00000334256.8:c.1210-208_1210-207del	ENSP00000334373.4:n.1210-208_1210-207del
ENST00000483437.1:c.253-208_253-207del	ENSP00000417172.1:n.253-208_253-207del
NM_002268.4:c.1210-208_1210-207del	NP_002259.1:n.1210-208_1210-207del
NM_002268.5:c.1210-208_1210-207del MANE Select	NP_002259.1:n.1210-208_1210-207del