Canonical Allele Identifier: CA412374484

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18911719G>A (hg19) ; chrX:g.18893601G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893601G>A , CM000685.2:g.18893601G>A	GRCh38
NC_000023.10:g.18911719G>A , CM000685.1:g.18911719G>A	GRCh37
NC_000023.9:g.18821640G>A	NCBI36
NG_016622.1:g.95762C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3592C>T (PHKA2) MANE Select	ENSP00000369274.4:p.His1198Tyr
ENST00000379942.4:c.3592C>T (PHKA2)	ENSP00000369274.4:p.His1198Tyr
ENST00000469485.5:n.1317C>T (PHKA2)
ENST00000473597.1:n.361C>T (PHKA2)
ENST00000481718.1:n.2486C>T (PHKA2)
NM_000292.2:c.3592C>T (PHKA2)	NP_000283.1:p.His1198Tyr
NR_029379.1:n.467+263G>A (PHKA2-AS1)
XM_005274548.3:c.3538C>T (PHKA2)	XP_005274605.1:p.His1180Tyr
XM_005274550.3:c.3508C>T (PHKA2)	XP_005274607.1:p.His1170Tyr
XM_006724496.2:c.3616C>T (PHKA2)	XP_006724559.1:p.His1206Tyr
XM_006724498.2:c.3070C>T (PHKA2)	XP_006724561.1:p.His1024Tyr
XM_011545537.1:c.3517C>T (PHKA2)	XP_011543839.1:p.His1173Tyr
XM_011545538.1:c.2599C>T (PHKA2)	XP_011543840.1:p.His867Tyr
XM_005274548.5:c.3538C>T (PHKA2)	XP_005274605.1:p.His1180Tyr
XM_005274550.5:c.3508C>T (PHKA2)	XP_005274607.1:p.His1170Tyr
XM_006724496.4:c.3616C>T (PHKA2)	XP_006724559.1:p.His1206Tyr
XM_006724498.4:c.3070C>T (PHKA2)	XP_006724561.1:p.His1024Tyr
XM_011545537.3:c.3517C>T (PHKA2)	XP_011543839.1:p.His1173Tyr
XM_011545538.3:c.2599C>T (PHKA2)	XP_011543840.1:p.His867Tyr
XM_017029580.2:c.2710C>T (PHKA2)	XP_016885069.1:p.His904Tyr
XR_001755698.2:n.5720C>T (PHKA2)
NM_000292.3:c.3592C>T (PHKA2) MANE Select	NP_000283.1:p.His1198Tyr