Canonical Allele Identifier: CA412374542

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18911733G>T (hg19) ; chrX:g.18893615G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893615G>T , CM000685.2:g.18893615G>T	GRCh38
NC_000023.10:g.18911733G>T , CM000685.1:g.18911733G>T	GRCh37
NC_000023.9:g.18821654G>T	NCBI36
NG_016622.1:g.95748C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3578C>A (PHKA2) MANE Select	ENSP00000369274.4:p.Ala1193Asp
ENST00000379942.4:c.3578C>A (PHKA2)	ENSP00000369274.4:p.Ala1193Asp
ENST00000469485.5:n.1303C>A (PHKA2)
ENST00000473597.1:n.347C>A (PHKA2)
ENST00000481718.1:n.2472C>A (PHKA2)
NM_000292.2:c.3578C>A (PHKA2)	NP_000283.1:p.Ala1193Asp
NR_029379.1:n.467+277G>T (PHKA2-AS1)
XM_005274548.3:c.3524C>A (PHKA2)	XP_005274605.1:p.Ala1175Asp
XM_005274550.3:c.3494C>A (PHKA2)	XP_005274607.1:p.Ala1165Asp
XM_006724496.2:c.3602C>A (PHKA2)	XP_006724559.1:p.Ala1201Asp
XM_006724498.2:c.3056C>A (PHKA2)	XP_006724561.1:p.Ala1019Asp
XM_011545537.1:c.3503C>A (PHKA2)	XP_011543839.1:p.Ala1168Asp
XM_011545538.1:c.2585C>A (PHKA2)	XP_011543840.1:p.Ala862Asp
XM_005274548.5:c.3524C>A (PHKA2)	XP_005274605.1:p.Ala1175Asp
XM_005274550.5:c.3494C>A (PHKA2)	XP_005274607.1:p.Ala1165Asp
XM_006724496.4:c.3602C>A (PHKA2)	XP_006724559.1:p.Ala1201Asp
XM_006724498.4:c.3056C>A (PHKA2)	XP_006724561.1:p.Ala1019Asp
XM_011545537.3:c.3503C>A (PHKA2)	XP_011543839.1:p.Ala1168Asp
XM_011545538.3:c.2585C>A (PHKA2)	XP_011543840.1:p.Ala862Asp
XM_017029580.2:c.2696C>A (PHKA2)	XP_016885069.1:p.Ala899Asp
XR_001755698.2:n.5706C>A (PHKA2)
NM_000292.3:c.3578C>A (PHKA2) MANE Select	NP_000283.1:p.Ala1193Asp