Canonical Allele Identifier: CA355202851

Gene: KPNA4

Linked Data

• MyVariant Identifiers: chr3:g.160226042G>A (hg19) ; chr3:g.160508254G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160508254G>A , CM000665.2:g.160508254G>A	GRCh38
NC_000003.11:g.160226042G>A , CM000665.1:g.160226042G>A	GRCh37
NC_000003.10:g.161708736G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334256.9:c.1225C>T MANE Select	ENSP00000334373.4:p.Gln409Ter
ENST00000483437.2:c.1225C>T	ENSP00000417172.2:p.Gln409Ter
ENST00000676799.1:c.*1174C>T	ENSP00000503839.1:n.*1174C>T
ENST00000676866.1:c.1153C>T	ENSP00000503291.1:p.Gln385Ter
ENST00000676958.1:c.1337C>T	ENSP00000503083.1:n.1337C>T
ENST00000678020.1:n.1405C>T
ENST00000678630.1:c.*1190C>T	ENSP00000504510.1:n.*1190C>T
ENST00000678765.1:c.1093C>T	ENSP00000503064.1:p.Gln365Ter
ENST00000334256.8:c.1225C>T	ENSP00000334373.4:p.Gln409Ter
ENST00000483437.1:c.268C>T	ENSP00000417172.1:p.Gln90Ter
NM_002268.4:c.1225C>T	NP_002259.1:p.Gln409Ter
NM_002268.5:c.1225C>T MANE Select	NP_002259.1:p.Gln409Ter