Canonical Allele Identifier: CA2090579991

Gene: KPNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.49731995T= , CM000675.2:g.49731995T=	GRCh38
NC_000013.10:g.50306131T= , CM000675.1:g.50306131T=	GRCh37
NC_000013.9:g.49204132T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261667.8:c.383+376A= MANE Select	ENSP00000261667.3:n.383+376A=
ENST00000261667.7:c.383+376A=	ENSP00000261667.3:n.383+376A=
NM_002267.3:c.383+376A=	NP_002258.2:n.383+376A=
XM_017020561.1:c.311+376A=	XP_016876050.1:n.311+376A=
NM_002267.4:c.383+376A= MANE Select	NP_002258.2:n.383+376A=