Canonical Allele Identifier: CA355202797

Gene: KPNA4

Linked Data

• MyVariant Identifiers: chr3:g.160226032A>C (hg19) ; chr3:g.160508244A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160508244A>C , CM000665.2:g.160508244A>C	GRCh38
NC_000003.11:g.160226032A>C , CM000665.1:g.160226032A>C	GRCh37
NC_000003.10:g.161708726A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334256.9:c.1235T>G MANE Select	ENSP00000334373.4:p.Val412Gly
ENST00000483437.2:c.1235T>G	ENSP00000417172.2:p.Val412Gly
ENST00000676799.1:c.*1184T>G	ENSP00000503839.1:n.*1184T>G
ENST00000676866.1:c.1163T>G	ENSP00000503291.1:p.Val388Gly
ENST00000676958.1:c.1347T>G	ENSP00000503083.1:n.1347T>G
ENST00000678020.1:n.1415T>G
ENST00000678630.1:c.*1200T>G	ENSP00000504510.1:n.*1200T>G
ENST00000678765.1:c.1103T>G	ENSP00000503064.1:p.Val368Gly
ENST00000334256.8:c.1235T>G	ENSP00000334373.4:p.Val412Gly
ENST00000483437.1:c.278T>G	ENSP00000417172.1:p.Val93Gly
NM_002268.4:c.1235T>G	NP_002259.1:p.Val412Gly
NM_002268.5:c.1235T>G MANE Select	NP_002259.1:p.Val412Gly