Canonical Allele Identifier: CA412374535

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18911731T>A (hg19) ; chrX:g.18893613T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893613T>A , CM000685.2:g.18893613T>A	GRCh38
NC_000023.10:g.18911731T>A , CM000685.1:g.18911731T>A	GRCh37
NC_000023.9:g.18821652T>A	NCBI36
NG_016622.1:g.95750A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379942.5:c.3580A>T (PHKA2) MANE Select	ENSP00000369274.4:p.Thr1194Ser
ENST00000379942.4:c.3580A>T (PHKA2)	ENSP00000369274.4:p.Thr1194Ser
ENST00000469485.5:n.1305A>T (PHKA2)
ENST00000473597.1:n.349A>T (PHKA2)
ENST00000481718.1:n.2474A>T (PHKA2)
NM_000292.2:c.3580A>T (PHKA2)	NP_000283.1:p.Thr1194Ser
NR_029379.1:n.467+275T>A (PHKA2-AS1)
XM_005274548.3:c.3526A>T (PHKA2)	XP_005274605.1:p.Thr1176Ser
XM_005274550.3:c.3496A>T (PHKA2)	XP_005274607.1:p.Thr1166Ser
XM_006724496.2:c.3604A>T (PHKA2)	XP_006724559.1:p.Thr1202Ser
XM_006724498.2:c.3058A>T (PHKA2)	XP_006724561.1:p.Thr1020Ser
XM_011545537.1:c.3505A>T (PHKA2)	XP_011543839.1:p.Thr1169Ser
XM_011545538.1:c.2587A>T (PHKA2)	XP_011543840.1:p.Thr863Ser
XM_005274548.5:c.3526A>T (PHKA2)	XP_005274605.1:p.Thr1176Ser
XM_005274550.5:c.3496A>T (PHKA2)	XP_005274607.1:p.Thr1166Ser
XM_006724496.4:c.3604A>T (PHKA2)	XP_006724559.1:p.Thr1202Ser
XM_006724498.4:c.3058A>T (PHKA2)	XP_006724561.1:p.Thr1020Ser
XM_011545537.3:c.3505A>T (PHKA2)	XP_011543839.1:p.Thr1169Ser
XM_011545538.3:c.2587A>T (PHKA2)	XP_011543840.1:p.Thr863Ser
XM_017029580.2:c.2698A>T (PHKA2)	XP_016885069.1:p.Thr900Ser
XR_001755698.2:n.5708A>T (PHKA2)
NM_000292.3:c.3580A>T (PHKA2) MANE Select	NP_000283.1:p.Thr1194Ser