Canonical Allele Identifier: CA412374694
Gene: PHKA2 HGNC NCBI
PHKA2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000379942.5:c.3544A>T (PHKA2) MANE Select ENSP00000369274.4:p.Ile1182Phe
ENST00000379942.4:c.3544A>T (PHKA2) ENSP00000369274.4:p.Ile1182Phe
ENST00000469485.5:n.1269A>T (PHKA2)
ENST00000473597.1:n.313A>T (PHKA2)
ENST00000481718.1:n.2438A>T (PHKA2)
NM_000292.2:c.3544A>T (PHKA2) NP_000283.1:p.Ile1182Phe
NR_029379.1:n.467+311T>A (PHKA2-AS1)
XM_005274548.3:c.3490A>T (PHKA2) XP_005274605.1:p.Ile1164Phe
XM_005274550.3:c.3460A>T (PHKA2) XP_005274607.1:p.Ile1154Phe
XM_006724496.2:c.3568A>T (PHKA2) XP_006724559.1:p.Ile1190Phe
XM_006724498.2:c.3022A>T (PHKA2) XP_006724561.1:p.Ile1008Phe
XM_011545537.1:c.3469A>T (PHKA2) XP_011543839.1:p.Ile1157Phe
XM_011545538.1:c.2551A>T (PHKA2) XP_011543840.1:p.Ile851Phe
XM_005274548.5:c.3490A>T (PHKA2) XP_005274605.1:p.Ile1164Phe
XM_005274550.5:c.3460A>T (PHKA2) XP_005274607.1:p.Ile1154Phe
XM_006724496.4:c.3568A>T (PHKA2) XP_006724559.1:p.Ile1190Phe
XM_006724498.4:c.3022A>T (PHKA2) XP_006724561.1:p.Ile1008Phe
XM_011545537.3:c.3469A>T (PHKA2) XP_011543839.1:p.Ile1157Phe
XM_011545538.3:c.2551A>T (PHKA2) XP_011543840.1:p.Ile851Phe
XM_017029580.2:c.2662A>T (PHKA2) XP_016885069.1:p.Ile888Phe
XR_001755698.2:n.5672A>T (PHKA2)
NM_000292.3:c.3544A>T (PHKA2) MANE Select NP_000283.1:p.Ile1182Phe