Canonical Allele Identifier: CA412374521

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18911727C>G (hg19) ; chrX:g.18893609C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893609C>G , CM000685.2:g.18893609C>G	GRCh38
NC_000023.10:g.18911727C>G , CM000685.1:g.18911727C>G	GRCh37
NC_000023.9:g.18821648C>G	NCBI36
NG_016622.1:g.95754G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3584G>C (PHKA2) MANE Select	ENSP00000369274.4:p.Gly1195Ala
ENST00000379942.4:c.3584G>C (PHKA2)	ENSP00000369274.4:p.Gly1195Ala
ENST00000469485.5:n.1309G>C (PHKA2)
ENST00000473597.1:n.353G>C (PHKA2)
ENST00000481718.1:n.2478G>C (PHKA2)
NM_000292.2:c.3584G>C (PHKA2)	NP_000283.1:p.Gly1195Ala
NR_029379.1:n.467+271C>G (PHKA2-AS1)
XM_005274548.3:c.3530G>C (PHKA2)	XP_005274605.1:p.Gly1177Ala
XM_005274550.3:c.3500G>C (PHKA2)	XP_005274607.1:p.Gly1167Ala
XM_006724496.2:c.3608G>C (PHKA2)	XP_006724559.1:p.Gly1203Ala
XM_006724498.2:c.3062G>C (PHKA2)	XP_006724561.1:p.Gly1021Ala
XM_011545537.1:c.3509G>C (PHKA2)	XP_011543839.1:p.Gly1170Ala
XM_011545538.1:c.2591G>C (PHKA2)	XP_011543840.1:p.Gly864Ala
XM_005274548.5:c.3530G>C (PHKA2)	XP_005274605.1:p.Gly1177Ala
XM_005274550.5:c.3500G>C (PHKA2)	XP_005274607.1:p.Gly1167Ala
XM_006724496.4:c.3608G>C (PHKA2)	XP_006724559.1:p.Gly1203Ala
XM_006724498.4:c.3062G>C (PHKA2)	XP_006724561.1:p.Gly1021Ala
XM_011545537.3:c.3509G>C (PHKA2)	XP_011543839.1:p.Gly1170Ala
XM_011545538.3:c.2591G>C (PHKA2)	XP_011543840.1:p.Gly864Ala
XM_017029580.2:c.2702G>C (PHKA2)	XP_016885069.1:p.Gly901Ala
XR_001755698.2:n.5712G>C (PHKA2)
NM_000292.3:c.3584G>C (PHKA2) MANE Select	NP_000283.1:p.Gly1195Ala