Canonical Allele Identifier: CA355202828

Gene: KPNA4

Linked Data

• MyVariant Identifiers: chr3:g.160226038T>C (hg19) ; chr3:g.160508250T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160508250T>C , CM000665.2:g.160508250T>C	GRCh38
NC_000003.11:g.160226038T>C , CM000665.1:g.160226038T>C	GRCh37
NC_000003.10:g.161708732T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334256.9:c.1229A>G MANE Select	ENSP00000334373.4:p.Gln410Arg
ENST00000483437.2:c.1229A>G	ENSP00000417172.2:p.Gln410Arg
ENST00000676799.1:c.*1178A>G	ENSP00000503839.1:n.*1178A>G
ENST00000676866.1:c.1157A>G	ENSP00000503291.1:p.Gln386Arg
ENST00000676958.1:c.1341A>G	ENSP00000503083.1:n.1341A>G
ENST00000678020.1:n.1409A>G
ENST00000678630.1:c.*1194A>G	ENSP00000504510.1:n.*1194A>G
ENST00000678765.1:c.1097A>G	ENSP00000503064.1:p.Gln366Arg
ENST00000334256.8:c.1229A>G	ENSP00000334373.4:p.Gln410Arg
ENST00000483437.1:c.272A>G	ENSP00000417172.1:p.Gln91Arg
NM_002268.4:c.1229A>G	NP_002259.1:p.Gln410Arg
NM_002268.5:c.1229A>G MANE Select	NP_002259.1:p.Gln410Arg