Canonical Allele Identifier: CA412374589

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18911744C>G (hg19) ; chrX:g.18893626C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893626C>G , CM000685.2:g.18893626C>G	GRCh38
NC_000023.10:g.18911744C>G , CM000685.1:g.18911744C>G	GRCh37
NC_000023.9:g.18821665C>G	NCBI36
NG_016622.1:g.95737G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3567G>C (PHKA2) MANE Select	ENSP00000369274.4:p.Glu1189Asp
ENST00000379942.4:c.3567G>C (PHKA2)	ENSP00000369274.4:p.Glu1189Asp
ENST00000469485.5:n.1292G>C (PHKA2)
ENST00000473597.1:n.336G>C (PHKA2)
ENST00000481718.1:n.2461G>C (PHKA2)
NM_000292.2:c.3567G>C (PHKA2)	NP_000283.1:p.Glu1189Asp
NR_029379.1:n.467+288C>G (PHKA2-AS1)
XM_005274548.3:c.3513G>C (PHKA2)	XP_005274605.1:p.Glu1171Asp
XM_005274550.3:c.3483G>C (PHKA2)	XP_005274607.1:p.Glu1161Asp
XM_006724496.2:c.3591G>C (PHKA2)	XP_006724559.1:p.Glu1197Asp
XM_006724498.2:c.3045G>C (PHKA2)	XP_006724561.1:p.Glu1015Asp
XM_011545537.1:c.3492G>C (PHKA2)	XP_011543839.1:p.Glu1164Asp
XM_011545538.1:c.2574G>C (PHKA2)	XP_011543840.1:p.Glu858Asp
XM_005274548.5:c.3513G>C (PHKA2)	XP_005274605.1:p.Glu1171Asp
XM_005274550.5:c.3483G>C (PHKA2)	XP_005274607.1:p.Glu1161Asp
XM_006724496.4:c.3591G>C (PHKA2)	XP_006724559.1:p.Glu1197Asp
XM_006724498.4:c.3045G>C (PHKA2)	XP_006724561.1:p.Glu1015Asp
XM_011545537.3:c.3492G>C (PHKA2)	XP_011543839.1:p.Glu1164Asp
XM_011545538.3:c.2574G>C (PHKA2)	XP_011543840.1:p.Glu858Asp
XM_017029580.2:c.2685G>C (PHKA2)	XP_016885069.1:p.Glu895Asp
XR_001755698.2:n.5695G>C (PHKA2)
NM_000292.3:c.3567G>C (PHKA2) MANE Select	NP_000283.1:p.Glu1189Asp