Canonical Allele Identifier: CA2090579988
Gene: KPNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.49731986T= , CM000675.2:g.49731986T= GRCh38
NC_000013.10:g.50306122T= , CM000675.1:g.50306122T= GRCh37
NC_000013.9:g.49204123T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261667.8:c.383+385A= MANE Select ENSP00000261667.3:n.383+385A=
ENST00000261667.7:c.383+385A= ENSP00000261667.3:n.383+385A=
NM_002267.3:c.383+385A= NP_002258.2:n.383+385A=
XM_017020561.1:c.311+385A= XP_016876050.1:n.311+385A=
NM_002267.4:c.383+385A= MANE Select NP_002258.2:n.383+385A=