Canonical Allele Identifier: CA412374633

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18911755C>A (hg19) ; chrX:g.18893637C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893637C>A , CM000685.2:g.18893637C>A	GRCh38
NC_000023.10:g.18911755C>A , CM000685.1:g.18911755C>A	GRCh37
NC_000023.9:g.18821676C>A	NCBI36
NG_016622.1:g.95726G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3556G>T (PHKA2) MANE Select	ENSP00000369274.4:p.Asp1186Tyr
ENST00000379942.4:c.3556G>T (PHKA2)	ENSP00000369274.4:p.Asp1186Tyr
ENST00000469485.5:n.1281G>T (PHKA2)
ENST00000473597.1:n.325G>T (PHKA2)
ENST00000481718.1:n.2450G>T (PHKA2)
NM_000292.2:c.3556G>T (PHKA2)	NP_000283.1:p.Asp1186Tyr
NR_029379.1:n.467+299C>A (PHKA2-AS1)
XM_005274548.3:c.3502G>T (PHKA2)	XP_005274605.1:p.Asp1168Tyr
XM_005274550.3:c.3472G>T (PHKA2)	XP_005274607.1:p.Asp1158Tyr
XM_006724496.2:c.3580G>T (PHKA2)	XP_006724559.1:p.Asp1194Tyr
XM_006724498.2:c.3034G>T (PHKA2)	XP_006724561.1:p.Asp1012Tyr
XM_011545537.1:c.3481G>T (PHKA2)	XP_011543839.1:p.Asp1161Tyr
XM_011545538.1:c.2563G>T (PHKA2)	XP_011543840.1:p.Asp855Tyr
XM_005274548.5:c.3502G>T (PHKA2)	XP_005274605.1:p.Asp1168Tyr
XM_005274550.5:c.3472G>T (PHKA2)	XP_005274607.1:p.Asp1158Tyr
XM_006724496.4:c.3580G>T (PHKA2)	XP_006724559.1:p.Asp1194Tyr
XM_006724498.4:c.3034G>T (PHKA2)	XP_006724561.1:p.Asp1012Tyr
XM_011545537.3:c.3481G>T (PHKA2)	XP_011543839.1:p.Asp1161Tyr
XM_011545538.3:c.2563G>T (PHKA2)	XP_011543840.1:p.Asp855Tyr
XM_017029580.2:c.2674G>T (PHKA2)	XP_016885069.1:p.Asp892Tyr
XR_001755698.2:n.5684G>T (PHKA2)
NM_000292.3:c.3556G>T (PHKA2) MANE Select	NP_000283.1:p.Asp1186Tyr