Canonical Allele Identifier: CA412374531

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18911730G>C (hg19) ; chrX:g.18893612G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893612G>C , CM000685.2:g.18893612G>C	GRCh38
NC_000023.10:g.18911730G>C , CM000685.1:g.18911730G>C	GRCh37
NC_000023.9:g.18821651G>C	NCBI36
NG_016622.1:g.95751C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3581C>G (PHKA2) MANE Select	ENSP00000369274.4:p.Thr1194Arg
ENST00000379942.4:c.3581C>G (PHKA2)	ENSP00000369274.4:p.Thr1194Arg
ENST00000469485.5:n.1306C>G (PHKA2)
ENST00000473597.1:n.350C>G (PHKA2)
ENST00000481718.1:n.2475C>G (PHKA2)
NM_000292.2:c.3581C>G (PHKA2)	NP_000283.1:p.Thr1194Arg
NR_029379.1:n.467+274G>C (PHKA2-AS1)
XM_005274548.3:c.3527C>G (PHKA2)	XP_005274605.1:p.Thr1176Arg
XM_005274550.3:c.3497C>G (PHKA2)	XP_005274607.1:p.Thr1166Arg
XM_006724496.2:c.3605C>G (PHKA2)	XP_006724559.1:p.Thr1202Arg
XM_006724498.2:c.3059C>G (PHKA2)	XP_006724561.1:p.Thr1020Arg
XM_011545537.1:c.3506C>G (PHKA2)	XP_011543839.1:p.Thr1169Arg
XM_011545538.1:c.2588C>G (PHKA2)	XP_011543840.1:p.Thr863Arg
XM_005274548.5:c.3527C>G (PHKA2)	XP_005274605.1:p.Thr1176Arg
XM_005274550.5:c.3497C>G (PHKA2)	XP_005274607.1:p.Thr1166Arg
XM_006724496.4:c.3605C>G (PHKA2)	XP_006724559.1:p.Thr1202Arg
XM_006724498.4:c.3059C>G (PHKA2)	XP_006724561.1:p.Thr1020Arg
XM_011545537.3:c.3506C>G (PHKA2)	XP_011543839.1:p.Thr1169Arg
XM_011545538.3:c.2588C>G (PHKA2)	XP_011543840.1:p.Thr863Arg
XM_017029580.2:c.2699C>G (PHKA2)	XP_016885069.1:p.Thr900Arg
XR_001755698.2:n.5709C>G (PHKA2)
NM_000292.3:c.3581C>G (PHKA2) MANE Select	NP_000283.1:p.Thr1194Arg