Canonical Allele Identifier: CA412374691

Gene: PHKA2 PHKA2-AS1

Linked Data

• gnomAD v4: X-18893648-A-T
• MyVariant Identifiers: chrX:g.18911766A>T (hg19) ; chrX:g.18893648A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893648A>T , CM000685.2:g.18893648A>T	GRCh38
NC_000023.10:g.18911766A>T , CM000685.1:g.18911766A>T	GRCh37
NC_000023.9:g.18821687A>T	NCBI36
NG_016622.1:g.95715T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3545T>A (PHKA2) MANE Select	ENSP00000369274.4:p.Ile1182Asn
ENST00000379942.4:c.3545T>A (PHKA2)	ENSP00000369274.4:p.Ile1182Asn
ENST00000469485.5:n.1270T>A (PHKA2)
ENST00000473597.1:n.314T>A (PHKA2)
ENST00000481718.1:n.2439T>A (PHKA2)
NM_000292.2:c.3545T>A (PHKA2)	NP_000283.1:p.Ile1182Asn
NR_029379.1:n.467+310A>T (PHKA2-AS1)
XM_005274548.3:c.3491T>A (PHKA2)	XP_005274605.1:p.Ile1164Asn
XM_005274550.3:c.3461T>A (PHKA2)	XP_005274607.1:p.Ile1154Asn
XM_006724496.2:c.3569T>A (PHKA2)	XP_006724559.1:p.Ile1190Asn
XM_006724498.2:c.3023T>A (PHKA2)	XP_006724561.1:p.Ile1008Asn
XM_011545537.1:c.3470T>A (PHKA2)	XP_011543839.1:p.Ile1157Asn
XM_011545538.1:c.2552T>A (PHKA2)	XP_011543840.1:p.Ile851Asn
XM_005274548.5:c.3491T>A (PHKA2)	XP_005274605.1:p.Ile1164Asn
XM_005274550.5:c.3461T>A (PHKA2)	XP_005274607.1:p.Ile1154Asn
XM_006724496.4:c.3569T>A (PHKA2)	XP_006724559.1:p.Ile1190Asn
XM_006724498.4:c.3023T>A (PHKA2)	XP_006724561.1:p.Ile1008Asn
XM_011545537.3:c.3470T>A (PHKA2)	XP_011543839.1:p.Ile1157Asn
XM_011545538.3:c.2552T>A (PHKA2)	XP_011543840.1:p.Ile851Asn
XM_017029580.2:c.2663T>A (PHKA2)	XP_016885069.1:p.Ile888Asn
XR_001755698.2:n.5673T>A (PHKA2)
NM_000292.3:c.3545T>A (PHKA2) MANE Select	NP_000283.1:p.Ile1182Asn