Canonical Allele Identifier: CA436486942

Gene: KPNA4

Linked Data

• MyVariant Identifiers: chr3:g.160226055C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160508267C>G , CM000665.2:g.160508267C>G	GRCh38
NC_000003.11:g.160226055C>G , CM000665.1:g.160226055C>G	GRCh37
NC_000003.10:g.161708749C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334256.9:c.1212G>C MANE Select	ENSP00000334373.4:p.Val404=
ENST00000483437.2:c.1212G>C	ENSP00000417172.2:p.Val404=
ENST00000676799.1:c.*1161G>C	ENSP00000503839.1:n.*1161G>C
ENST00000676866.1:c.1140G>C	ENSP00000503291.1:p.Val380=
ENST00000676958.1:c.1324G>C	ENSP00000503083.1:n.1324G>C
ENST00000678020.1:n.1392G>C
ENST00000678630.1:c.*1177G>C	ENSP00000504510.1:n.*1177G>C
ENST00000678765.1:c.1080G>C	ENSP00000503064.1:p.Val360=
ENST00000334256.8:c.1212G>C	ENSP00000334373.4:p.Val404=
ENST00000483437.1:c.255G>C	ENSP00000417172.1:p.Val85=
NM_002268.4:c.1212G>C	NP_002259.1:p.Val404=
NM_002268.5:c.1212G>C MANE Select	NP_002259.1:p.Val404=