Canonical Allele Identifier: CA2418071820

Gene: PHKA2 PHKA2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18893591_18893594delinsTAAA , CM000685.2:g.18893591_18893594delinsTAAA	GRCh38
NC_000023.10:g.18911709_18911712delinsTAAA , CM000685.1:g.18911709_18911712delinsTAAA	GRCh37
NC_000023.9:g.18821630_18821633delinsTAAA	NCBI36
NG_016622.1:g.95769_95772delinsTTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000379942.5:c.3599_3602delinsTTTA (PHKA2) MANE Select	ENSP00000369274.4:p.Phe1200=
ENST00000379942.4:c.3599_3602delinsTTTA (PHKA2)	ENSP00000369274.4:p.Phe1200=
ENST00000469485.5:n.1324_1327delinsTTTA (PHKA2)
ENST00000473597.1:n.368_371delinsTTTA (PHKA2)
ENST00000481718.1:n.2493_2496delinsTTTA (PHKA2)
NM_000292.2:c.3599_3602delinsTTTA (PHKA2)	NP_000283.1:p.Phe1200=
NR_029379.1:n.467+253_467+256delinsTAAA (PHKA2-AS1)
XM_005274548.3:c.3545_3548delinsTTTA (PHKA2)	XP_005274605.1:p.Phe1182=
XM_005274550.3:c.3515_3518delinsTTTA (PHKA2)	XP_005274607.1:p.Phe1172=
XM_006724496.2:c.3623_3626delinsTTTA (PHKA2)	XP_006724559.1:p.Phe1208=
XM_006724498.2:c.3077_3080delinsTTTA (PHKA2)	XP_006724561.1:p.Phe1026=
XM_011545537.1:c.3524_3527delinsTTTA (PHKA2)	XP_011543839.1:p.Phe1175=
XM_011545538.1:c.2606_2609delinsTTTA (PHKA2)	XP_011543840.1:p.Phe869=
XM_005274548.5:c.3545_3548delinsTTTA (PHKA2)	XP_005274605.1:p.Phe1182=
XM_005274550.5:c.3515_3518delinsTTTA (PHKA2)	XP_005274607.1:p.Phe1172=
XM_006724496.4:c.3623_3626delinsTTTA (PHKA2)	XP_006724559.1:p.Phe1208=
XM_006724498.4:c.3077_3080delinsTTTA (PHKA2)	XP_006724561.1:p.Phe1026=
XM_011545537.3:c.3524_3527delinsTTTA (PHKA2)	XP_011543839.1:p.Phe1175=
XM_011545538.3:c.2606_2609delinsTTTA (PHKA2)	XP_011543840.1:p.Phe869=
XM_017029580.2:c.2717_2720delinsTTTA (PHKA2)	XP_016885069.1:p.Phe906=
XR_001755698.2:n.5727_5730delinsTTTA (PHKA2)
NM_000292.3:c.3599_3602delinsTTTA (PHKA2) MANE Select	NP_000283.1:p.Phe1200=