Canonical Allele Identifier: CA412374551

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18911735T>A (hg19) ; chrX:g.18893617T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893617T>A , CM000685.2:g.18893617T>A	GRCh38
NC_000023.10:g.18911735T>A , CM000685.1:g.18911735T>A	GRCh37
NC_000023.9:g.18821656T>A	NCBI36
NG_016622.1:g.95746A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3576A>T (PHKA2) MANE Select	ENSP00000369274.4:p.Gln1192His
ENST00000379942.4:c.3576A>T (PHKA2)	ENSP00000369274.4:p.Gln1192His
ENST00000469485.5:n.1301A>T (PHKA2)
ENST00000473597.1:n.345A>T (PHKA2)
ENST00000481718.1:n.2470A>T (PHKA2)
NM_000292.2:c.3576A>T (PHKA2)	NP_000283.1:p.Gln1192His
NR_029379.1:n.467+279T>A (PHKA2-AS1)
XM_005274548.3:c.3522A>T (PHKA2)	XP_005274605.1:p.Gln1174His
XM_005274550.3:c.3492A>T (PHKA2)	XP_005274607.1:p.Gln1164His
XM_006724496.2:c.3600A>T (PHKA2)	XP_006724559.1:p.Gln1200His
XM_006724498.2:c.3054A>T (PHKA2)	XP_006724561.1:p.Gln1018His
XM_011545537.1:c.3501A>T (PHKA2)	XP_011543839.1:p.Gln1167His
XM_011545538.1:c.2583A>T (PHKA2)	XP_011543840.1:p.Gln861His
XM_005274548.5:c.3522A>T (PHKA2)	XP_005274605.1:p.Gln1174His
XM_005274550.5:c.3492A>T (PHKA2)	XP_005274607.1:p.Gln1164His
XM_006724496.4:c.3600A>T (PHKA2)	XP_006724559.1:p.Gln1200His
XM_006724498.4:c.3054A>T (PHKA2)	XP_006724561.1:p.Gln1018His
XM_011545537.3:c.3501A>T (PHKA2)	XP_011543839.1:p.Gln1167His
XM_011545538.3:c.2583A>T (PHKA2)	XP_011543840.1:p.Gln861His
XM_017029580.2:c.2694A>T (PHKA2)	XP_016885069.1:p.Gln898His
XR_001755698.2:n.5704A>T (PHKA2)
NM_000292.3:c.3576A>T (PHKA2) MANE Select	NP_000283.1:p.Gln1192His