Canonical Allele Identifier: CA901529358

Gene: KPNA4

Linked Data

• dbSNP Id: rs1264905926
• MyVariant Identifiers: chr3:g.160226126A>C (hg19) ; chr3:g.160508338A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160508338A>C , CM000665.2:g.160508338A>C	GRCh38
NC_000003.11:g.160226126A>C , CM000665.1:g.160226126A>C	GRCh37
NC_000003.10:g.161708820A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334256.9:c.1210-69T>G MANE Select	ENSP00000334373.4:n.1210-69T>G
ENST00000483437.2:c.1210-69T>G	ENSP00000417172.2:n.1210-69T>G
ENST00000676799.1:c.*1159-69T>G	ENSP00000503839.1:n.*1159-69T>G
ENST00000676866.1:c.1138-69T>G	ENSP00000503291.1:n.1138-69T>G
ENST00000676958.1:c.1322-69T>G	ENSP00000503083.1:n.1322-69T>G
ENST00000678020.1:n.1390-69T>G
ENST00000678630.1:c.*1175-69T>G	ENSP00000504510.1:n.*1175-69T>G
ENST00000678765.1:c.1078-69T>G	ENSP00000503064.1:n.1078-69T>G
ENST00000334256.8:c.1210-69T>G	ENSP00000334373.4:n.1210-69T>G
ENST00000483437.1:c.253-69T>G	ENSP00000417172.1:n.253-69T>G
NM_002268.4:c.1210-69T>G	NP_002259.1:n.1210-69T>G
NM_002268.5:c.1210-69T>G MANE Select	NP_002259.1:n.1210-69T>G