Canonical Allele Identifier: CA412374529

Gene: PHKA2 PHKA2-AS1

Linked Data

• COSMIC: COSM4750724
• MyVariant Identifiers: chrX:g.18911728C>A (hg19) ; chrX:g.18893610C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893610C>A , CM000685.2:g.18893610C>A	GRCh38
NC_000023.10:g.18911728C>A , CM000685.1:g.18911728C>A	GRCh37
NC_000023.9:g.18821649C>A	NCBI36
NG_016622.1:g.95753G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3583G>T (PHKA2) MANE Select	ENSP00000369274.4:p.Gly1195Ter
ENST00000379942.4:c.3583G>T (PHKA2)	ENSP00000369274.4:p.Gly1195Ter
ENST00000469485.5:n.1308G>T (PHKA2)
ENST00000473597.1:n.352G>T (PHKA2)
ENST00000481718.1:n.2477G>T (PHKA2)
NM_000292.2:c.3583G>T (PHKA2)	NP_000283.1:p.Gly1195Ter
NR_029379.1:n.467+272C>A (PHKA2-AS1)
XM_005274548.3:c.3529G>T (PHKA2)	XP_005274605.1:p.Gly1177Ter
XM_005274550.3:c.3499G>T (PHKA2)	XP_005274607.1:p.Gly1167Ter
XM_006724496.2:c.3607G>T (PHKA2)	XP_006724559.1:p.Gly1203Ter
XM_006724498.2:c.3061G>T (PHKA2)	XP_006724561.1:p.Gly1021Ter
XM_011545537.1:c.3508G>T (PHKA2)	XP_011543839.1:p.Gly1170Ter
XM_011545538.1:c.2590G>T (PHKA2)	XP_011543840.1:p.Gly864Ter
XM_005274548.5:c.3529G>T (PHKA2)	XP_005274605.1:p.Gly1177Ter
XM_005274550.5:c.3499G>T (PHKA2)	XP_005274607.1:p.Gly1167Ter
XM_006724496.4:c.3607G>T (PHKA2)	XP_006724559.1:p.Gly1203Ter
XM_006724498.4:c.3061G>T (PHKA2)	XP_006724561.1:p.Gly1021Ter
XM_011545537.3:c.3508G>T (PHKA2)	XP_011543839.1:p.Gly1170Ter
XM_011545538.3:c.2590G>T (PHKA2)	XP_011543840.1:p.Gly864Ter
XM_017029580.2:c.2701G>T (PHKA2)	XP_016885069.1:p.Gly901Ter
XR_001755698.2:n.5711G>T (PHKA2)
NM_000292.3:c.3583G>T (PHKA2) MANE Select	NP_000283.1:p.Gly1195Ter