Canonical Allele Identifier: CA655069122
Gene: KPNA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.49732013T>G , CM000675.2:g.49732013T>G GRCh38
NC_000013.10:g.50306149T>G , CM000675.1:g.50306149T>G GRCh37
NC_000013.9:g.49204150T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261667.8:c.383+358A>C MANE Select ENSP00000261667.3:n.383+358A>C
ENST00000261667.7:c.383+358A>C ENSP00000261667.3:n.383+358A>C
NM_002267.3:c.383+358A>C NP_002258.2:n.383+358A>C
XM_017020561.1:c.311+358A>C XP_016876050.1:n.311+358A>C
NM_002267.4:c.383+358A>C MANE Select NP_002258.2:n.383+358A>C