Canonical Allele Identifier: CA412374568

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18911739T>G (hg19) ; chrX:g.18893621T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893621T>G , CM000685.2:g.18893621T>G	GRCh38
NC_000023.10:g.18911739T>G , CM000685.1:g.18911739T>G	GRCh37
NC_000023.9:g.18821660T>G	NCBI36
NG_016622.1:g.95742A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3572A>C (PHKA2) MANE Select	ENSP00000369274.4:p.Asp1191Ala
ENST00000379942.4:c.3572A>C (PHKA2)	ENSP00000369274.4:p.Asp1191Ala
ENST00000469485.5:n.1297A>C (PHKA2)
ENST00000473597.1:n.341A>C (PHKA2)
ENST00000481718.1:n.2466A>C (PHKA2)
NM_000292.2:c.3572A>C (PHKA2)	NP_000283.1:p.Asp1191Ala
NR_029379.1:n.467+283T>G (PHKA2-AS1)
XM_005274548.3:c.3518A>C (PHKA2)	XP_005274605.1:p.Asp1173Ala
XM_005274550.3:c.3488A>C (PHKA2)	XP_005274607.1:p.Asp1163Ala
XM_006724496.2:c.3596A>C (PHKA2)	XP_006724559.1:p.Asp1199Ala
XM_006724498.2:c.3050A>C (PHKA2)	XP_006724561.1:p.Asp1017Ala
XM_011545537.1:c.3497A>C (PHKA2)	XP_011543839.1:p.Asp1166Ala
XM_011545538.1:c.2579A>C (PHKA2)	XP_011543840.1:p.Asp860Ala
XM_005274548.5:c.3518A>C (PHKA2)	XP_005274605.1:p.Asp1173Ala
XM_005274550.5:c.3488A>C (PHKA2)	XP_005274607.1:p.Asp1163Ala
XM_006724496.4:c.3596A>C (PHKA2)	XP_006724559.1:p.Asp1199Ala
XM_006724498.4:c.3050A>C (PHKA2)	XP_006724561.1:p.Asp1017Ala
XM_011545537.3:c.3497A>C (PHKA2)	XP_011543839.1:p.Asp1166Ala
XM_011545538.3:c.2579A>C (PHKA2)	XP_011543840.1:p.Asp860Ala
XM_017029580.2:c.2690A>C (PHKA2)	XP_016885069.1:p.Asp897Ala
XR_001755698.2:n.5700A>C (PHKA2)
NM_000292.3:c.3572A>C (PHKA2) MANE Select	NP_000283.1:p.Asp1191Ala