Canonical Allele Identifier: CA2090580161
Gene: KPNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.49732172T= , CM000675.2:g.49732172T= GRCh38
NC_000013.10:g.50306308T= , CM000675.1:g.50306308T= GRCh37
NC_000013.9:g.49204309T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261667.8:c.383+199A= MANE Select ENSP00000261667.3:n.383+199A=
ENST00000261667.7:c.383+199A= ENSP00000261667.3:n.383+199A=
NM_002267.3:c.383+199A= NP_002258.2:n.383+199A=
XM_017020561.1:c.311+199A= XP_016876050.1:n.311+199A=
NM_002267.4:c.383+199A= MANE Select NP_002258.2:n.383+199A=