Canonical Allele Identifier: CA436486939

Gene: KPNA4

Linked Data

• MyVariant Identifiers: chr3:g.160226052A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160508264A>T , CM000665.2:g.160508264A>T	GRCh38
NC_000003.11:g.160226052A>T , CM000665.1:g.160226052A>T	GRCh37
NC_000003.10:g.161708746A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334256.9:c.1215T>A MANE Select	ENSP00000334373.4:p.Ala405=
ENST00000483437.2:c.1215T>A	ENSP00000417172.2:p.Ala405=
ENST00000676799.1:c.*1164T>A	ENSP00000503839.1:n.*1164T>A
ENST00000676866.1:c.1143T>A	ENSP00000503291.1:p.Ala381=
ENST00000676958.1:c.1327T>A	ENSP00000503083.1:n.1327T>A
ENST00000678020.1:n.1395T>A
ENST00000678630.1:c.*1180T>A	ENSP00000504510.1:n.*1180T>A
ENST00000678765.1:c.1083T>A	ENSP00000503064.1:p.Ala361=
ENST00000334256.8:c.1215T>A	ENSP00000334373.4:p.Ala405=
ENST00000483437.1:c.258T>A	ENSP00000417172.1:p.Ala86=
NM_002268.4:c.1215T>A	NP_002259.1:p.Ala405=
NM_002268.5:c.1215T>A MANE Select	NP_002259.1:p.Ala405=