Canonical Allele Identifier: CA412374488
Gene: PHKA2 HGNC NCBI
PHKA2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18893601G>T , CM000685.2:g.18893601G>T GRCh38
NC_000023.10:g.18911719G>T , CM000685.1:g.18911719G>T GRCh37
NC_000023.9:g.18821640G>T NCBI36
NG_016622.1:g.95762C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379942.5:c.3592C>A (PHKA2) MANE Select ENSP00000369274.4:p.His1198Asn
ENST00000379942.4:c.3592C>A (PHKA2) ENSP00000369274.4:p.His1198Asn
ENST00000469485.5:n.1317C>A (PHKA2)
ENST00000473597.1:n.361C>A (PHKA2)
ENST00000481718.1:n.2486C>A (PHKA2)
NM_000292.2:c.3592C>A (PHKA2) NP_000283.1:p.His1198Asn
NR_029379.1:n.467+263G>T (PHKA2-AS1)
XM_005274548.3:c.3538C>A (PHKA2) XP_005274605.1:p.His1180Asn
XM_005274550.3:c.3508C>A (PHKA2) XP_005274607.1:p.His1170Asn
XM_006724496.2:c.3616C>A (PHKA2) XP_006724559.1:p.His1206Asn
XM_006724498.2:c.3070C>A (PHKA2) XP_006724561.1:p.His1024Asn
XM_011545537.1:c.3517C>A (PHKA2) XP_011543839.1:p.His1173Asn
XM_011545538.1:c.2599C>A (PHKA2) XP_011543840.1:p.His867Asn
XM_005274548.5:c.3538C>A (PHKA2) XP_005274605.1:p.His1180Asn
XM_005274550.5:c.3508C>A (PHKA2) XP_005274607.1:p.His1170Asn
XM_006724496.4:c.3616C>A (PHKA2) XP_006724559.1:p.His1206Asn
XM_006724498.4:c.3070C>A (PHKA2) XP_006724561.1:p.His1024Asn
XM_011545537.3:c.3517C>A (PHKA2) XP_011543839.1:p.His1173Asn
XM_011545538.3:c.2599C>A (PHKA2) XP_011543840.1:p.His867Asn
XM_017029580.2:c.2710C>A (PHKA2) XP_016885069.1:p.His904Asn
XR_001755698.2:n.5720C>A (PHKA2)
NM_000292.3:c.3592C>A (PHKA2) MANE Select NP_000283.1:p.His1198Asn