Canonical Allele Identifier: CA412374395

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18911700G>T (hg19) ; chrX:g.18893582G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893582G>T , CM000685.2:g.18893582G>T	GRCh38
NC_000023.10:g.18911700G>T , CM000685.1:g.18911700G>T	GRCh37
NC_000023.9:g.18821621G>T	NCBI36
NG_016622.1:g.95781C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3611C>A (PHKA2) MANE Select	ENSP00000369274.4:p.Ala1204Asp
ENST00000379942.4:c.3611C>A (PHKA2)	ENSP00000369274.4:p.Ala1204Asp
ENST00000469485.5:n.1336C>A (PHKA2)
ENST00000473597.1:n.380C>A (PHKA2)
ENST00000481718.1:n.2505C>A (PHKA2)
NM_000292.2:c.3611C>A (PHKA2)	NP_000283.1:p.Ala1204Asp
NR_029379.1:n.467+244G>T (PHKA2-AS1)
XM_005274548.3:c.3557C>A (PHKA2)	XP_005274605.1:p.Ala1186Asp
XM_005274550.3:c.3527C>A (PHKA2)	XP_005274607.1:p.Ala1176Asp
XM_006724496.2:c.3635C>A (PHKA2)	XP_006724559.1:p.Ala1212Asp
XM_006724498.2:c.3089C>A (PHKA2)	XP_006724561.1:p.Ala1030Asp
XM_011545537.1:c.3536C>A (PHKA2)	XP_011543839.1:p.Ala1179Asp
XM_011545538.1:c.2618C>A (PHKA2)	XP_011543840.1:p.Ala873Asp
XM_005274548.5:c.3557C>A (PHKA2)	XP_005274605.1:p.Ala1186Asp
XM_005274550.5:c.3527C>A (PHKA2)	XP_005274607.1:p.Ala1176Asp
XM_006724496.4:c.3635C>A (PHKA2)	XP_006724559.1:p.Ala1212Asp
XM_006724498.4:c.3089C>A (PHKA2)	XP_006724561.1:p.Ala1030Asp
XM_011545537.3:c.3536C>A (PHKA2)	XP_011543839.1:p.Ala1179Asp
XM_011545538.3:c.2618C>A (PHKA2)	XP_011543840.1:p.Ala873Asp
XM_017029580.2:c.2729C>A (PHKA2)	XP_016885069.1:p.Ala910Asp
XR_001755698.2:n.5739C>A (PHKA2)
NM_000292.3:c.3611C>A (PHKA2) MANE Select	NP_000283.1:p.Ala1204Asp