Canonical Allele Identifier: CA2570061056

Gene: PHKA2 PHKA2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18894407A>G , CM000685.2:g.18894407A>G	GRCh38
NC_000023.10:g.18912525A>G , CM000685.1:g.18912525A>G	GRCh37
NC_000023.9:g.18822446A>G	NCBI36
NG_016622.1:g.94956T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3337-3T>C (PHKA2) MANE Select	ENSP00000369274.4:n.3337-3T>C
ENST00000379942.4:c.3337-3T>C (PHKA2)	ENSP00000369274.4:n.3337-3T>C
ENST00000469485.5:n.1062-3T>C (PHKA2)
ENST00000473597.1:n.106-3T>C (PHKA2)
ENST00000473739.5:n.429-3T>C (PHKA2)
ENST00000481718.1:n.2228T>C (PHKA2)
NM_000292.2:c.3337-3T>C (PHKA2)	NP_000283.1:n.3337-3T>C
NR_029379.1:n.728A>G (PHKA2-AS1)
XM_005274548.3:c.3283-3T>C (PHKA2)	XP_005274605.1:n.3283-3T>C
XM_005274550.3:c.3253-3T>C (PHKA2)	XP_005274607.1:n.3253-3T>C
XM_006724496.2:c.3361-3T>C (PHKA2)	XP_006724559.1:n.3361-3T>C
XM_006724498.2:c.2815-3T>C (PHKA2)	XP_006724561.1:n.2815-3T>C
XM_011545537.1:c.3262-3T>C (PHKA2)	XP_011543839.1:n.3262-3T>C
XM_011545538.1:c.2344-3T>C (PHKA2)	XP_011543840.1:n.2344-3T>C
XM_005274548.5:c.3283-3T>C (PHKA2)	XP_005274605.1:n.3283-3T>C
XM_005274550.5:c.3253-3T>C (PHKA2)	XP_005274607.1:n.3253-3T>C
XM_006724496.4:c.3361-3T>C (PHKA2)	XP_006724559.1:n.3361-3T>C
XM_006724498.4:c.2815-3T>C (PHKA2)	XP_006724561.1:n.2815-3T>C
XM_011545537.3:c.3262-3T>C (PHKA2)	XP_011543839.1:n.3262-3T>C
XM_011545538.3:c.2344-3T>C (PHKA2)	XP_011543840.1:n.2344-3T>C
XM_017029580.2:c.2455-3T>C (PHKA2)	XP_016885069.1:n.2455-3T>C
XR_001755698.2:n.5465-3T>C (PHKA2)
XR_002958777.1:n.3542-3T>C (PHKA2)
NM_000292.3:c.3337-3T>C (PHKA2) MANE Select	NP_000283.1:n.3337-3T>C