Canonical Allele Identifier: CA2693234335
Gene: PHKA2 HGNC NCBI
PHKA2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18894423_18894426del , CM000685.2:g.18894423_18894426del GRCh38
NC_000023.10:g.18912541_18912544del , CM000685.1:g.18912541_18912544del GRCh37
NC_000023.9:g.18822462_18822465del NCBI36
NG_016622.1:g.94943_94946del

Transcript Alleles

HGVS Amino-acid change
ENST00000379942.5:c.3337-16_3337-13del (PHKA2) MANE Select ENSP00000369274.4:n.3337-16_3337-13del
ENST00000379942.4:c.3337-16_3337-13del (PHKA2) ENSP00000369274.4:n.3337-16_3337-13del
ENST00000469485.5:n.1062-16_1062-13del (PHKA2)
ENST00000473597.1:n.106-16_106-13del (PHKA2)
ENST00000473739.5:n.429-16_429-13del (PHKA2)
ENST00000481718.1:n.2215_2218del (PHKA2)
NM_000292.2:c.3337-16_3337-13del (PHKA2) NP_000283.1:n.3337-16_3337-13del
NR_029379.1:n.744_747del (PHKA2-AS1)
XM_005274548.3:c.3283-16_3283-13del (PHKA2) XP_005274605.1:n.3283-16_3283-13del
XM_005274550.3:c.3253-16_3253-13del (PHKA2) XP_005274607.1:n.3253-16_3253-13del
XM_006724496.2:c.3361-16_3361-13del (PHKA2) XP_006724559.1:n.3361-16_3361-13del
XM_006724498.2:c.2815-16_2815-13del (PHKA2) XP_006724561.1:n.2815-16_2815-13del
XM_011545537.1:c.3262-16_3262-13del (PHKA2) XP_011543839.1:n.3262-16_3262-13del
XM_011545538.1:c.2344-16_2344-13del (PHKA2) XP_011543840.1:n.2344-16_2344-13del
XM_005274548.5:c.3283-16_3283-13del (PHKA2) XP_005274605.1:n.3283-16_3283-13del
XM_005274550.5:c.3253-16_3253-13del (PHKA2) XP_005274607.1:n.3253-16_3253-13del
XM_006724496.4:c.3361-16_3361-13del (PHKA2) XP_006724559.1:n.3361-16_3361-13del
XM_006724498.4:c.2815-16_2815-13del (PHKA2) XP_006724561.1:n.2815-16_2815-13del
XM_011545537.3:c.3262-16_3262-13del (PHKA2) XP_011543839.1:n.3262-16_3262-13del
XM_011545538.3:c.2344-16_2344-13del (PHKA2) XP_011543840.1:n.2344-16_2344-13del
XM_017029580.2:c.2455-16_2455-13del (PHKA2) XP_016885069.1:n.2455-16_2455-13del
XR_001755698.2:n.5465-16_5465-13del (PHKA2)
XR_002958777.1:n.3542-16_3542-13del (PHKA2)
NM_000292.3:c.3337-16_3337-13del (PHKA2) MANE Select NP_000283.1:n.3337-16_3337-13del