Canonical Allele Identifier: CA1415222192
Gene: KPNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.160508264A= , CM000665.2:g.160508264A= GRCh38
NC_000003.11:g.160226052A= , CM000665.1:g.160226052A= GRCh37
NC_000003.10:g.161708746A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000334256.9:c.1215T= MANE Select ENSP00000334373.4:p.Ala405=
ENST00000483437.2:c.1215T= ENSP00000417172.2:p.Ala405=
ENST00000676799.1:c.*1164T= ENSP00000503839.1:n.*1164T=
ENST00000676866.1:c.1143T= ENSP00000503291.1:p.Ala381=
ENST00000676958.1:c.1327T= ENSP00000503083.1:n.1327T=
ENST00000678020.1:n.1395T=
ENST00000678630.1:c.*1180T= ENSP00000504510.1:n.*1180T=
ENST00000678765.1:c.1083T= ENSP00000503064.1:p.Ala361=
ENST00000334256.8:c.1215T= ENSP00000334373.4:p.Ala405=
ENST00000483437.1:c.258T= ENSP00000417172.1:p.Ala86=
NM_002268.4:c.1215T= NP_002259.1:p.Ala405=
NM_002268.5:c.1215T= MANE Select NP_002259.1:p.Ala405=