Canonical Allele Identifier: CA2418071818
Gene: PHKA2 HGNC NCBI
PHKA2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18893583C= , CM000685.2:g.18893583C= GRCh38
NC_000023.10:g.18911701C= , CM000685.1:g.18911701C= GRCh37
NC_000023.9:g.18821622C= NCBI36
NG_016622.1:g.95780G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379942.5:c.3610G= (PHKA2) MANE Select ENSP00000369274.4:p.Ala1204=
ENST00000379942.4:c.3610G= (PHKA2) ENSP00000369274.4:p.Ala1204=
ENST00000469485.5:n.1335G= (PHKA2)
ENST00000473597.1:n.379G= (PHKA2)
ENST00000481718.1:n.2504G= (PHKA2)
NM_000292.2:c.3610G= (PHKA2) NP_000283.1:p.Ala1204=
NR_029379.1:n.467+245C= (PHKA2-AS1)
XM_005274548.3:c.3556G= (PHKA2) XP_005274605.1:p.Ala1186=
XM_005274550.3:c.3526G= (PHKA2) XP_005274607.1:p.Ala1176=
XM_006724496.2:c.3634G= (PHKA2) XP_006724559.1:p.Ala1212=
XM_006724498.2:c.3088G= (PHKA2) XP_006724561.1:p.Ala1030=
XM_011545537.1:c.3535G= (PHKA2) XP_011543839.1:p.Ala1179=
XM_011545538.1:c.2617G= (PHKA2) XP_011543840.1:p.Ala873=
XM_005274548.5:c.3556G= (PHKA2) XP_005274605.1:p.Ala1186=
XM_005274550.5:c.3526G= (PHKA2) XP_005274607.1:p.Ala1176=
XM_006724496.4:c.3634G= (PHKA2) XP_006724559.1:p.Ala1212=
XM_006724498.4:c.3088G= (PHKA2) XP_006724561.1:p.Ala1030=
XM_011545537.3:c.3535G= (PHKA2) XP_011543839.1:p.Ala1179=
XM_011545538.3:c.2617G= (PHKA2) XP_011543840.1:p.Ala873=
XM_017029580.2:c.2728G= (PHKA2) XP_016885069.1:p.Ala910=
XR_001755698.2:n.5738G= (PHKA2)
NM_000292.3:c.3610G= (PHKA2) MANE Select NP_000283.1:p.Ala1204=