Canonical Allele Identifier: CA10361316
Community Standard Title: NM_000292.3(PHKA2):c.3357G>A (p.Lys1119=)
Gene: PHKA2 HGNC NCBI
PHKA2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18894384C>T , CM000685.2:g.18894384C>T GRCh38
NC_000023.10:g.18912502C>T , CM000685.1:g.18912502C>T GRCh37
NC_000023.9:g.18822423C>T NCBI36
NG_016622.1:g.94979G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000292.3:c.3357G>A (PHKA2) MANE Select NP_000283.1:p.Lys1119=
ENST00000379942.5:c.3357G>A (PHKA2) MANE Select ENSP00000369274.4:p.Lys1119=
NM_000292.2:c.3357G>A (PHKA2) NP_000283.1:p.Lys1119=
NR_029379.1:n.705C>T (PHKA2-AS1)
ENST00000379942.4:c.3357G>A (PHKA2) ENSP00000369274.4:p.Lys1119=
ENST00000469485.5:n.1082G>A (PHKA2)
ENST00000473597.1:n.126G>A (PHKA2)
ENST00000473739.5:n.449G>A (PHKA2)
ENST00000481718.1:n.2251G>A (PHKA2)
XM_005274548.3:c.3303G>A (PHKA2) XP_005274605.1:p.Lys1101=
XM_005274548.5:c.3303G>A (PHKA2) XP_005274605.1:p.Lys1101=
XM_005274550.3:c.3273G>A (PHKA2) XP_005274607.1:p.Lys1091=
XM_005274550.5:c.3273G>A (PHKA2) XP_005274607.1:p.Lys1091=
XM_006724496.2:c.3381G>A (PHKA2) XP_006724559.1:p.Lys1127=
XM_006724496.4:c.3381G>A (PHKA2) XP_006724559.1:p.Lys1127=
XM_006724498.2:c.2835G>A (PHKA2) XP_006724561.1:p.Lys945=
XM_006724498.4:c.2835G>A (PHKA2) XP_006724561.1:p.Lys945=
XM_011545537.1:c.3282G>A (PHKA2) XP_011543839.1:p.Lys1094=
XM_011545537.3:c.3282G>A (PHKA2) XP_011543839.1:p.Lys1094=
XM_011545538.1:c.2364G>A (PHKA2) XP_011543840.1:p.Lys788=
XM_011545538.3:c.2364G>A (PHKA2) XP_011543840.1:p.Lys788=
XM_017029580.2:c.2475G>A (PHKA2) XP_016885069.1:p.Lys825=
XR_001755698.2:n.5485G>A (PHKA2)
XR_002958777.1:n.3562G>A (PHKA2)