Canonical Allele Identifier: CA1415222453
Gene: KPNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.160508496A= , CM000665.2:g.160508496A= GRCh38
NC_000003.11:g.160226284A= , CM000665.1:g.160226284A= GRCh37
NC_000003.10:g.161708978A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000334256.9:c.1210-227T= MANE Select ENSP00000334373.4:n.1210-227T=
ENST00000483437.2:c.1210-227T= ENSP00000417172.2:n.1210-227T=
ENST00000676799.1:c.*1159-227T= ENSP00000503839.1:n.*1159-227T=
ENST00000676866.1:c.1138-227T= ENSP00000503291.1:n.1138-227T=
ENST00000676958.1:c.1322-227T= ENSP00000503083.1:n.1322-227T=
ENST00000678020.1:n.1390-227T=
ENST00000678630.1:c.*1175-227T= ENSP00000504510.1:n.*1175-227T=
ENST00000678765.1:c.1078-227T= ENSP00000503064.1:n.1078-227T=
ENST00000334256.8:c.1210-227T= ENSP00000334373.4:n.1210-227T=
ENST00000483437.1:c.253-227T= ENSP00000417172.1:n.253-227T=
NM_002268.4:c.1210-227T= NP_002259.1:n.1210-227T=
NM_002268.5:c.1210-227T= MANE Select NP_002259.1:n.1210-227T=