Canonical Allele Identifier: CA327026050
Gene: PHKA2 HGNC NCBI
PHKA2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs749043832
gnomAD v3: X-18894408-C-A
gnomAD v4: X-18894408-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18894408C>A , CM000685.2:g.18894408C>A GRCh38
NC_000023.10:g.18912526C>A , CM000685.1:g.18912526C>A GRCh37
NC_000023.9:g.18822447C>A NCBI36
NG_016622.1:g.94955G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379942.5:c.3337-4G>T (PHKA2) MANE Select ENSP00000369274.4:n.3337-4G>T
ENST00000379942.4:c.3337-4G>T (PHKA2) ENSP00000369274.4:n.3337-4G>T
ENST00000469485.5:n.1062-4G>T (PHKA2)
ENST00000473597.1:n.106-4G>T (PHKA2)
ENST00000473739.5:n.429-4G>T (PHKA2)
ENST00000481718.1:n.2227G>T (PHKA2)
NM_000292.2:c.3337-4G>T (PHKA2) NP_000283.1:n.3337-4G>T
NR_029379.1:n.729C>A (PHKA2-AS1)
XM_005274548.3:c.3283-4G>T (PHKA2) XP_005274605.1:n.3283-4G>T
XM_005274550.3:c.3253-4G>T (PHKA2) XP_005274607.1:n.3253-4G>T
XM_006724496.2:c.3361-4G>T (PHKA2) XP_006724559.1:n.3361-4G>T
XM_006724498.2:c.2815-4G>T (PHKA2) XP_006724561.1:n.2815-4G>T
XM_011545537.1:c.3262-4G>T (PHKA2) XP_011543839.1:n.3262-4G>T
XM_011545538.1:c.2344-4G>T (PHKA2) XP_011543840.1:n.2344-4G>T
XM_005274548.5:c.3283-4G>T (PHKA2) XP_005274605.1:n.3283-4G>T
XM_005274550.5:c.3253-4G>T (PHKA2) XP_005274607.1:n.3253-4G>T
XM_006724496.4:c.3361-4G>T (PHKA2) XP_006724559.1:n.3361-4G>T
XM_006724498.4:c.2815-4G>T (PHKA2) XP_006724561.1:n.2815-4G>T
XM_011545537.3:c.3262-4G>T (PHKA2) XP_011543839.1:n.3262-4G>T
XM_011545538.3:c.2344-4G>T (PHKA2) XP_011543840.1:n.2344-4G>T
XM_017029580.2:c.2455-4G>T (PHKA2) XP_016885069.1:n.2455-4G>T
XR_001755698.2:n.5465-4G>T (PHKA2)
XR_002958777.1:n.3542-4G>T (PHKA2)
NM_000292.3:c.3337-4G>T (PHKA2) MANE Select NP_000283.1:n.3337-4G>T