Canonical Allele Identifier: CA412374503

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18911722A>G (hg19) ; chrX:g.18893604A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893604A>G , CM000685.2:g.18893604A>G	GRCh38
NC_000023.10:g.18911722A>G , CM000685.1:g.18911722A>G	GRCh37
NC_000023.9:g.18821643A>G	NCBI36
NG_016622.1:g.95759T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3589T>C (PHKA2) MANE Select	ENSP00000369274.4:p.Cys1197Arg
ENST00000379942.4:c.3589T>C (PHKA2)	ENSP00000369274.4:p.Cys1197Arg
ENST00000469485.5:n.1314T>C (PHKA2)
ENST00000473597.1:n.358T>C (PHKA2)
ENST00000481718.1:n.2483T>C (PHKA2)
NM_000292.2:c.3589T>C (PHKA2)	NP_000283.1:p.Cys1197Arg
NR_029379.1:n.467+266A>G (PHKA2-AS1)
XM_005274548.3:c.3535T>C (PHKA2)	XP_005274605.1:p.Cys1179Arg
XM_005274550.3:c.3505T>C (PHKA2)	XP_005274607.1:p.Cys1169Arg
XM_006724496.2:c.3613T>C (PHKA2)	XP_006724559.1:p.Cys1205Arg
XM_006724498.2:c.3067T>C (PHKA2)	XP_006724561.1:p.Cys1023Arg
XM_011545537.1:c.3514T>C (PHKA2)	XP_011543839.1:p.Cys1172Arg
XM_011545538.1:c.2596T>C (PHKA2)	XP_011543840.1:p.Cys866Arg
XM_005274548.5:c.3535T>C (PHKA2)	XP_005274605.1:p.Cys1179Arg
XM_005274550.5:c.3505T>C (PHKA2)	XP_005274607.1:p.Cys1169Arg
XM_006724496.4:c.3613T>C (PHKA2)	XP_006724559.1:p.Cys1205Arg
XM_006724498.4:c.3067T>C (PHKA2)	XP_006724561.1:p.Cys1023Arg
XM_011545537.3:c.3514T>C (PHKA2)	XP_011543839.1:p.Cys1172Arg
XM_011545538.3:c.2596T>C (PHKA2)	XP_011543840.1:p.Cys866Arg
XM_017029580.2:c.2707T>C (PHKA2)	XP_016885069.1:p.Cys903Arg
XR_001755698.2:n.5717T>C (PHKA2)
NM_000292.3:c.3589T>C (PHKA2) MANE Select	NP_000283.1:p.Cys1197Arg