Canonical Allele Identifier: CA412374604
Gene: PHKA2 HGNC NCBI
PHKA2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18893630A>C , CM000685.2:g.18893630A>C GRCh38
NC_000023.10:g.18911748A>C , CM000685.1:g.18911748A>C GRCh37
NC_000023.9:g.18821669A>C NCBI36
NG_016622.1:g.95733T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379942.5:c.3563T>G (PHKA2) MANE Select ENSP00000369274.4:p.Leu1188Arg
ENST00000379942.4:c.3563T>G (PHKA2) ENSP00000369274.4:p.Leu1188Arg
ENST00000469485.5:n.1288T>G (PHKA2)
ENST00000473597.1:n.332T>G (PHKA2)
ENST00000481718.1:n.2457T>G (PHKA2)
NM_000292.2:c.3563T>G (PHKA2) NP_000283.1:p.Leu1188Arg
NR_029379.1:n.467+292A>C (PHKA2-AS1)
XM_005274548.3:c.3509T>G (PHKA2) XP_005274605.1:p.Leu1170Arg
XM_005274550.3:c.3479T>G (PHKA2) XP_005274607.1:p.Leu1160Arg
XM_006724496.2:c.3587T>G (PHKA2) XP_006724559.1:p.Leu1196Arg
XM_006724498.2:c.3041T>G (PHKA2) XP_006724561.1:p.Leu1014Arg
XM_011545537.1:c.3488T>G (PHKA2) XP_011543839.1:p.Leu1163Arg
XM_011545538.1:c.2570T>G (PHKA2) XP_011543840.1:p.Leu857Arg
XM_005274548.5:c.3509T>G (PHKA2) XP_005274605.1:p.Leu1170Arg
XM_005274550.5:c.3479T>G (PHKA2) XP_005274607.1:p.Leu1160Arg
XM_006724496.4:c.3587T>G (PHKA2) XP_006724559.1:p.Leu1196Arg
XM_006724498.4:c.3041T>G (PHKA2) XP_006724561.1:p.Leu1014Arg
XM_011545537.3:c.3488T>G (PHKA2) XP_011543839.1:p.Leu1163Arg
XM_011545538.3:c.2570T>G (PHKA2) XP_011543840.1:p.Leu857Arg
XM_017029580.2:c.2681T>G (PHKA2) XP_016885069.1:p.Leu894Arg
XR_001755698.2:n.5691T>G (PHKA2)
NM_000292.3:c.3563T>G (PHKA2) MANE Select NP_000283.1:p.Leu1188Arg