Canonical Allele Identifier: CA412376255

Gene: PHKA2 PHKA2-AS1

Linked Data

• MyVariant Identifiers: chrX:g.18912518G>T (hg19) ; chrX:g.18894400G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18894400G>T , CM000685.2:g.18894400G>T	GRCh38
NC_000023.10:g.18912518G>T , CM000685.1:g.18912518G>T	GRCh37
NC_000023.9:g.18822439G>T	NCBI36
NG_016622.1:g.94963C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000379942.5:c.3341C>A (PHKA2) MANE Select	ENSP00000369274.4:p.Thr1114Asn
ENST00000379942.4:c.3341C>A (PHKA2)	ENSP00000369274.4:p.Thr1114Asn
ENST00000469485.5:n.1066C>A (PHKA2)
ENST00000473597.1:n.110C>A (PHKA2)
ENST00000473739.5:n.433C>A (PHKA2)
ENST00000481718.1:n.2235C>A (PHKA2)
NM_000292.2:c.3341C>A (PHKA2)	NP_000283.1:p.Thr1114Asn
NR_029379.1:n.721G>T (PHKA2-AS1)
XM_005274548.3:c.3287C>A (PHKA2)	XP_005274605.1:p.Thr1096Asn
XM_005274550.3:c.3257C>A (PHKA2)	XP_005274607.1:p.Thr1086Asn
XM_006724496.2:c.3365C>A (PHKA2)	XP_006724559.1:p.Thr1122Asn
XM_006724498.2:c.2819C>A (PHKA2)	XP_006724561.1:p.Thr940Asn
XM_011545537.1:c.3266C>A (PHKA2)	XP_011543839.1:p.Thr1089Asn
XM_011545538.1:c.2348C>A (PHKA2)	XP_011543840.1:p.Thr783Asn
XM_005274548.5:c.3287C>A (PHKA2)	XP_005274605.1:p.Thr1096Asn
XM_005274550.5:c.3257C>A (PHKA2)	XP_005274607.1:p.Thr1086Asn
XM_006724496.4:c.3365C>A (PHKA2)	XP_006724559.1:p.Thr1122Asn
XM_006724498.4:c.2819C>A (PHKA2)	XP_006724561.1:p.Thr940Asn
XM_011545537.3:c.3266C>A (PHKA2)	XP_011543839.1:p.Thr1089Asn
XM_011545538.3:c.2348C>A (PHKA2)	XP_011543840.1:p.Thr783Asn
XM_017029580.2:c.2459C>A (PHKA2)	XP_016885069.1:p.Thr820Asn
XR_001755698.2:n.5469C>A (PHKA2)
XR_002958777.1:n.3546C>A (PHKA2)
NM_000292.3:c.3341C>A (PHKA2) MANE Select	NP_000283.1:p.Thr1114Asn