Canonical Allele Identifier: CA2090580139
Gene: KPNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.49732153A= , CM000675.2:g.49732153A= GRCh38
NC_000013.10:g.50306289A= , CM000675.1:g.50306289A= GRCh37
NC_000013.9:g.49204290A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261667.8:c.383+218T= MANE Select ENSP00000261667.3:n.383+218T=
ENST00000261667.7:c.383+218T= ENSP00000261667.3:n.383+218T=
NM_002267.3:c.383+218T= NP_002258.2:n.383+218T=
XM_017020561.1:c.311+218T= XP_016876050.1:n.311+218T=
NM_002267.4:c.383+218T= MANE Select NP_002258.2:n.383+218T=