Canonical Allele Identifier: CA2418091460

Gene: PHKA2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18951173G= , CM000685.2:g.18951173G=	GRCh38
NC_000023.10:g.18969291G= , CM000685.1:g.18969291G=	GRCh37
NC_000023.9:g.18879212G=	NCBI36
NG_016622.1:g.38190C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379942.5:c.385C= MANE Select	ENSP00000369274.4:p.Gln129=
ENST00000379942.4:c.385C=	ENSP00000369274.4:p.Gln129=
NM_000292.2:c.385C=	NP_000283.1:p.Gln129=
XM_005274548.3:c.385C=	XP_005274605.1:p.Gln129=
XM_005274550.3:c.385C=	XP_005274607.1:p.Gln129=
XM_006724496.2:c.385C=	XP_006724559.1:p.Gln129=
XM_006724498.2:c.-93+1321C=	XP_006724561.1:n.-93+1321C=
XM_011545537.1:c.385C=	XP_011543839.1:p.Gln129=
XR_950461.1:n.569C=
XM_005274548.5:c.385C=	XP_005274605.1:p.Gln129=
XM_005274550.5:c.385C=	XP_005274607.1:p.Gln129=
XM_006724496.4:c.385C=	XP_006724559.1:p.Gln129=
XM_006724498.4:c.-93+1321C=	XP_006724561.1:n.-93+1321C=
XM_011545537.3:c.385C=	XP_011543839.1:p.Gln129=
XM_017029580.2:c.-457C=	XP_016885069.1:n.-457C=
XR_001755697.2:n.555C=
XR_001755698.2:n.555C=
XR_002958777.1:n.555C=
XR_950461.3:n.555C=
NM_000292.3:c.385C= MANE Select	NP_000283.1:p.Gln129=