Canonical Allele Identifier: CA412374438

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18911709T>G (hg19) ; chrX:g.18893591T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893591T>G , CM000685.2:g.18893591T>G	GRCh38
NC_000023.10:g.18911709T>G , CM000685.1:g.18911709T>G	GRCh37
NC_000023.9:g.18821630T>G	NCBI36
NG_016622.1:g.95772A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3602A>C (PHKA2) MANE Select	ENSP00000369274.4:p.Tyr1201Ser
ENST00000379942.4:c.3602A>C (PHKA2)	ENSP00000369274.4:p.Tyr1201Ser
ENST00000469485.5:n.1327A>C (PHKA2)
ENST00000473597.1:n.371A>C (PHKA2)
ENST00000481718.1:n.2496A>C (PHKA2)
NM_000292.2:c.3602A>C (PHKA2)	NP_000283.1:p.Tyr1201Ser
NR_029379.1:n.467+253T>G (PHKA2-AS1)
XM_005274548.3:c.3548A>C (PHKA2)	XP_005274605.1:p.Tyr1183Ser
XM_005274550.3:c.3518A>C (PHKA2)	XP_005274607.1:p.Tyr1173Ser
XM_006724496.2:c.3626A>C (PHKA2)	XP_006724559.1:p.Tyr1209Ser
XM_006724498.2:c.3080A>C (PHKA2)	XP_006724561.1:p.Tyr1027Ser
XM_011545537.1:c.3527A>C (PHKA2)	XP_011543839.1:p.Tyr1176Ser
XM_011545538.1:c.2609A>C (PHKA2)	XP_011543840.1:p.Tyr870Ser
XM_005274548.5:c.3548A>C (PHKA2)	XP_005274605.1:p.Tyr1183Ser
XM_005274550.5:c.3518A>C (PHKA2)	XP_005274607.1:p.Tyr1173Ser
XM_006724496.4:c.3626A>C (PHKA2)	XP_006724559.1:p.Tyr1209Ser
XM_006724498.4:c.3080A>C (PHKA2)	XP_006724561.1:p.Tyr1027Ser
XM_011545537.3:c.3527A>C (PHKA2)	XP_011543839.1:p.Tyr1176Ser
XM_011545538.3:c.2609A>C (PHKA2)	XP_011543840.1:p.Tyr870Ser
XM_017029580.2:c.2720A>C (PHKA2)	XP_016885069.1:p.Tyr907Ser
XR_001755698.2:n.5730A>C (PHKA2)
NM_000292.3:c.3602A>C (PHKA2) MANE Select	NP_000283.1:p.Tyr1201Ser