Canonical Allele Identifier: CA86605421

Gene: KPNA4

Linked Data

• dbSNP Id: rs952022927
• gnomAD v3: 3-160508321-C-T
• gnomAD v4: 3-160508321-C-T
• MyVariant Identifiers: chr3:g.160226109C>T (hg19) ; chr3:g.160508321C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160508321C>T , CM000665.2:g.160508321C>T	GRCh38
NC_000003.11:g.160226109C>T , CM000665.1:g.160226109C>T	GRCh37
NC_000003.10:g.161708803C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334256.9:c.1210-52G>A MANE Select	ENSP00000334373.4:n.1210-52G>A
ENST00000483437.2:c.1210-52G>A	ENSP00000417172.2:n.1210-52G>A
ENST00000676799.1:c.*1159-52G>A	ENSP00000503839.1:n.*1159-52G>A
ENST00000676866.1:c.1138-52G>A	ENSP00000503291.1:n.1138-52G>A
ENST00000676958.1:c.1322-52G>A	ENSP00000503083.1:n.1322-52G>A
ENST00000678020.1:n.1390-52G>A
ENST00000678630.1:c.*1175-52G>A	ENSP00000504510.1:n.*1175-52G>A
ENST00000678765.1:c.1078-52G>A	ENSP00000503064.1:n.1078-52G>A
ENST00000334256.8:c.1210-52G>A	ENSP00000334373.4:n.1210-52G>A
ENST00000483437.1:c.253-52G>A	ENSP00000417172.1:n.253-52G>A
NM_002268.4:c.1210-52G>A	NP_002259.1:n.1210-52G>A
NM_002268.5:c.1210-52G>A MANE Select	NP_002259.1:n.1210-52G>A