Canonical Allele Identifier: CA2668394352

Gene: KPNA4

Linked Data

• gnomAD v4: 3-160508347-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160508347G>T , CM000665.2:g.160508347G>T	GRCh38
NC_000003.11:g.160226135G>T , CM000665.1:g.160226135G>T	GRCh37
NC_000003.10:g.161708829G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000334256.9:c.1210-78C>A MANE Select	ENSP00000334373.4:n.1210-78C>A
ENST00000483437.2:c.1210-78C>A	ENSP00000417172.2:n.1210-78C>A
ENST00000676799.1:c.*1159-78C>A	ENSP00000503839.1:n.*1159-78C>A
ENST00000676866.1:c.1138-78C>A	ENSP00000503291.1:n.1138-78C>A
ENST00000676958.1:c.1322-78C>A	ENSP00000503083.1:n.1322-78C>A
ENST00000678020.1:n.1390-78C>A
ENST00000678630.1:c.*1175-78C>A	ENSP00000504510.1:n.*1175-78C>A
ENST00000678765.1:c.1078-78C>A	ENSP00000503064.1:n.1078-78C>A
ENST00000334256.8:c.1210-78C>A	ENSP00000334373.4:n.1210-78C>A
ENST00000483437.1:c.253-78C>A	ENSP00000417172.1:n.253-78C>A
NM_002268.4:c.1210-78C>A	NP_002259.1:n.1210-78C>A
NM_002268.5:c.1210-78C>A MANE Select	NP_002259.1:n.1210-78C>A