Canonical Allele Identifier: CA2418071838
Gene: PHKA2 HGNC NCBI
PHKA2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18893649T= , CM000685.2:g.18893649T= GRCh38
NC_000023.10:g.18911767T= , CM000685.1:g.18911767T= GRCh37
NC_000023.9:g.18821688T= NCBI36
NG_016622.1:g.95714A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379942.5:c.3544A= (PHKA2) MANE Select ENSP00000369274.4:p.Ile1182=
ENST00000379942.4:c.3544A= (PHKA2) ENSP00000369274.4:p.Ile1182=
ENST00000469485.5:n.1269A= (PHKA2)
ENST00000473597.1:n.313A= (PHKA2)
ENST00000481718.1:n.2438A= (PHKA2)
NM_000292.2:c.3544A= (PHKA2) NP_000283.1:p.Ile1182=
NR_029379.1:n.467+311T= (PHKA2-AS1)
XM_005274548.3:c.3490A= (PHKA2) XP_005274605.1:p.Ile1164=
XM_005274550.3:c.3460A= (PHKA2) XP_005274607.1:p.Ile1154=
XM_006724496.2:c.3568A= (PHKA2) XP_006724559.1:p.Ile1190=
XM_006724498.2:c.3022A= (PHKA2) XP_006724561.1:p.Ile1008=
XM_011545537.1:c.3469A= (PHKA2) XP_011543839.1:p.Ile1157=
XM_011545538.1:c.2551A= (PHKA2) XP_011543840.1:p.Ile851=
XM_005274548.5:c.3490A= (PHKA2) XP_005274605.1:p.Ile1164=
XM_005274550.5:c.3460A= (PHKA2) XP_005274607.1:p.Ile1154=
XM_006724496.4:c.3568A= (PHKA2) XP_006724559.1:p.Ile1190=
XM_006724498.4:c.3022A= (PHKA2) XP_006724561.1:p.Ile1008=
XM_011545537.3:c.3469A= (PHKA2) XP_011543839.1:p.Ile1157=
XM_011545538.3:c.2551A= (PHKA2) XP_011543840.1:p.Ile851=
XM_017029580.2:c.2662A= (PHKA2) XP_016885069.1:p.Ile888=
XR_001755698.2:n.5672A= (PHKA2)
NM_000292.3:c.3544A= (PHKA2) MANE Select NP_000283.1:p.Ile1182=