Canonical Allele Identifier: CA412374662

Gene: PHKA2 PHKA2-AS1

Linked Data

• dbSNP Id: rs2047470583
• MyVariant Identifiers: chrX:g.18911760G>C (hg19) ; chrX:g.18893642G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893642G>C , CM000685.2:g.18893642G>C	GRCh38
NC_000023.10:g.18911760G>C , CM000685.1:g.18911760G>C	GRCh37
NC_000023.9:g.18821681G>C	NCBI36
NG_016622.1:g.95721C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3551C>G (PHKA2) MANE Select	ENSP00000369274.4:p.Ala1184Gly
ENST00000379942.4:c.3551C>G (PHKA2)	ENSP00000369274.4:p.Ala1184Gly
ENST00000469485.5:n.1276C>G (PHKA2)
ENST00000473597.1:n.320C>G (PHKA2)
ENST00000481718.1:n.2445C>G (PHKA2)
NM_000292.2:c.3551C>G (PHKA2)	NP_000283.1:p.Ala1184Gly
NR_029379.1:n.467+304G>C (PHKA2-AS1)
XM_005274548.3:c.3497C>G (PHKA2)	XP_005274605.1:p.Ala1166Gly
XM_005274550.3:c.3467C>G (PHKA2)	XP_005274607.1:p.Ala1156Gly
XM_006724496.2:c.3575C>G (PHKA2)	XP_006724559.1:p.Ala1192Gly
XM_006724498.2:c.3029C>G (PHKA2)	XP_006724561.1:p.Ala1010Gly
XM_011545537.1:c.3476C>G (PHKA2)	XP_011543839.1:p.Ala1159Gly
XM_011545538.1:c.2558C>G (PHKA2)	XP_011543840.1:p.Ala853Gly
XM_005274548.5:c.3497C>G (PHKA2)	XP_005274605.1:p.Ala1166Gly
XM_005274550.5:c.3467C>G (PHKA2)	XP_005274607.1:p.Ala1156Gly
XM_006724496.4:c.3575C>G (PHKA2)	XP_006724559.1:p.Ala1192Gly
XM_006724498.4:c.3029C>G (PHKA2)	XP_006724561.1:p.Ala1010Gly
XM_011545537.3:c.3476C>G (PHKA2)	XP_011543839.1:p.Ala1159Gly
XM_011545538.3:c.2558C>G (PHKA2)	XP_011543840.1:p.Ala853Gly
XM_017029580.2:c.2669C>G (PHKA2)	XP_016885069.1:p.Ala890Gly
XR_001755698.2:n.5679C>G (PHKA2)
NM_000292.3:c.3551C>G (PHKA2) MANE Select	NP_000283.1:p.Ala1184Gly