Canonical Allele Identifier: CA412374582

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18911742T>G (hg19) ; chrX:g.18893624T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893624T>G , CM000685.2:g.18893624T>G	GRCh38
NC_000023.10:g.18911742T>G , CM000685.1:g.18911742T>G	GRCh37
NC_000023.9:g.18821663T>G	NCBI36
NG_016622.1:g.95739A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3569A>C (PHKA2) MANE Select	ENSP00000369274.4:p.Lys1190Thr
ENST00000379942.4:c.3569A>C (PHKA2)	ENSP00000369274.4:p.Lys1190Thr
ENST00000469485.5:n.1294A>C (PHKA2)
ENST00000473597.1:n.338A>C (PHKA2)
ENST00000481718.1:n.2463A>C (PHKA2)
NM_000292.2:c.3569A>C (PHKA2)	NP_000283.1:p.Lys1190Thr
NR_029379.1:n.467+286T>G (PHKA2-AS1)
XM_005274548.3:c.3515A>C (PHKA2)	XP_005274605.1:p.Lys1172Thr
XM_005274550.3:c.3485A>C (PHKA2)	XP_005274607.1:p.Lys1162Thr
XM_006724496.2:c.3593A>C (PHKA2)	XP_006724559.1:p.Lys1198Thr
XM_006724498.2:c.3047A>C (PHKA2)	XP_006724561.1:p.Lys1016Thr
XM_011545537.1:c.3494A>C (PHKA2)	XP_011543839.1:p.Lys1165Thr
XM_011545538.1:c.2576A>C (PHKA2)	XP_011543840.1:p.Lys859Thr
XM_005274548.5:c.3515A>C (PHKA2)	XP_005274605.1:p.Lys1172Thr
XM_005274550.5:c.3485A>C (PHKA2)	XP_005274607.1:p.Lys1162Thr
XM_006724496.4:c.3593A>C (PHKA2)	XP_006724559.1:p.Lys1198Thr
XM_006724498.4:c.3047A>C (PHKA2)	XP_006724561.1:p.Lys1016Thr
XM_011545537.3:c.3494A>C (PHKA2)	XP_011543839.1:p.Lys1165Thr
XM_011545538.3:c.2576A>C (PHKA2)	XP_011543840.1:p.Lys859Thr
XM_017029580.2:c.2687A>C (PHKA2)	XP_016885069.1:p.Lys896Thr
XR_001755698.2:n.5697A>C (PHKA2)
NM_000292.3:c.3569A>C (PHKA2) MANE Select	NP_000283.1:p.Lys1190Thr