Canonical Allele Identifier: CA412376290

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18912521A>G (hg19) ; chrX:g.18894403A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18894403A>G , CM000685.2:g.18894403A>G	GRCh38
NC_000023.10:g.18912521A>G , CM000685.1:g.18912521A>G	GRCh37
NC_000023.9:g.18822442A>G	NCBI36
NG_016622.1:g.94960T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379942.5:c.3338T>C (PHKA2) MANE Select	ENSP00000369274.4:p.Met1113Thr
ENST00000379942.4:c.3338T>C (PHKA2)	ENSP00000369274.4:p.Met1113Thr
ENST00000469485.5:n.1063T>C (PHKA2)
ENST00000473597.1:n.107T>C (PHKA2)
ENST00000473739.5:n.430T>C (PHKA2)
ENST00000481718.1:n.2232T>C (PHKA2)
NM_000292.2:c.3338T>C (PHKA2)	NP_000283.1:p.Met1113Thr
NR_029379.1:n.724A>G (PHKA2-AS1)
XM_005274548.3:c.3284T>C (PHKA2)	XP_005274605.1:p.Met1095Thr
XM_005274550.3:c.3254T>C (PHKA2)	XP_005274607.1:p.Met1085Thr
XM_006724496.2:c.3362T>C (PHKA2)	XP_006724559.1:p.Met1121Thr
XM_006724498.2:c.2816T>C (PHKA2)	XP_006724561.1:p.Met939Thr
XM_011545537.1:c.3263T>C (PHKA2)	XP_011543839.1:p.Met1088Thr
XM_011545538.1:c.2345T>C (PHKA2)	XP_011543840.1:p.Met782Thr
XM_005274548.5:c.3284T>C (PHKA2)	XP_005274605.1:p.Met1095Thr
XM_005274550.5:c.3254T>C (PHKA2)	XP_005274607.1:p.Met1085Thr
XM_006724496.4:c.3362T>C (PHKA2)	XP_006724559.1:p.Met1121Thr
XM_006724498.4:c.2816T>C (PHKA2)	XP_006724561.1:p.Met939Thr
XM_011545537.3:c.3263T>C (PHKA2)	XP_011543839.1:p.Met1088Thr
XM_011545538.3:c.2345T>C (PHKA2)	XP_011543840.1:p.Met782Thr
XM_017029580.2:c.2456T>C (PHKA2)	XP_016885069.1:p.Met819Thr
XR_001755698.2:n.5466T>C (PHKA2)
XR_002958777.1:n.3543T>C (PHKA2)
NM_000292.3:c.3338T>C (PHKA2) MANE Select	NP_000283.1:p.Met1113Thr