Canonical Allele Identifier: CA355202896

Gene: KPNA4

Linked Data

• gnomAD v4: 3-160508263-A-G
• MyVariant Identifiers: chr3:g.160226051A>G (hg19) ; chr3:g.160508263A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160508263A>G , CM000665.2:g.160508263A>G	GRCh38
NC_000003.11:g.160226051A>G , CM000665.1:g.160226051A>G	GRCh37
NC_000003.10:g.161708745A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334256.9:c.1216T>C MANE Select	ENSP00000334373.4:p.Tyr406His
ENST00000483437.2:c.1216T>C	ENSP00000417172.2:p.Tyr406His
ENST00000676799.1:c.*1165T>C	ENSP00000503839.1:n.*1165T>C
ENST00000676866.1:c.1144T>C	ENSP00000503291.1:p.Tyr382His
ENST00000676958.1:c.1328T>C	ENSP00000503083.1:n.1328T>C
ENST00000678020.1:n.1396T>C
ENST00000678630.1:c.*1181T>C	ENSP00000504510.1:n.*1181T>C
ENST00000678765.1:c.1084T>C	ENSP00000503064.1:p.Tyr362His
ENST00000334256.8:c.1216T>C	ENSP00000334373.4:p.Tyr406His
ENST00000483437.1:c.259T>C	ENSP00000417172.1:p.Tyr87His
NM_002268.4:c.1216T>C	NP_002259.1:p.Tyr406His
NM_002268.5:c.1216T>C MANE Select	NP_002259.1:p.Tyr406His