Canonical Allele Identifier: CA86605571
Gene: KPNA4 HGNC NCBI

Linked Data

dbSNP Id: rs17236529

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.160508519C>T , CM000665.2:g.160508519C>T GRCh38
NC_000003.11:g.160226307C>T , CM000665.1:g.160226307C>T GRCh37
NC_000003.10:g.161709001C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000334256.9:c.1210-250G>A MANE Select ENSP00000334373.4:n.1210-250G>A
ENST00000483437.2:c.1210-250G>A ENSP00000417172.2:n.1210-250G>A
ENST00000676799.1:c.*1159-250G>A ENSP00000503839.1:n.*1159-250G>A
ENST00000676866.1:c.1138-250G>A ENSP00000503291.1:n.1138-250G>A
ENST00000676958.1:c.1322-250G>A ENSP00000503083.1:n.1322-250G>A
ENST00000678020.1:n.1390-250G>A
ENST00000678630.1:c.*1175-250G>A ENSP00000504510.1:n.*1175-250G>A
ENST00000678765.1:c.1078-250G>A ENSP00000503064.1:n.1078-250G>A
ENST00000334256.8:c.1210-250G>A ENSP00000334373.4:n.1210-250G>A
ENST00000483437.1:c.253-250G>A ENSP00000417172.1:n.253-250G>A
NM_002268.4:c.1210-250G>A NP_002259.1:n.1210-250G>A
NM_002268.5:c.1210-250G>A MANE Select NP_002259.1:n.1210-250G>A