Canonical Allele Identifier: CA2418077729

Gene: PHKA2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18908865G= , CM000685.2:g.18908865G=	GRCh38
NC_000023.10:g.18926983G= , CM000685.1:g.18926983G=	GRCh37
NC_000023.9:g.18836904G=	NCBI36
NG_016622.1:g.80498C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000292.3:c.2296C= MANE Select	NP_000283.1:p.Gln766=
ENST00000379942.5:c.2296C= MANE Select	ENSP00000369274.4:p.Gln766=
NM_000292.2:c.2296C=	NP_000283.1:p.Gln766=
ENST00000379942.4:c.2296C=	ENSP00000369274.4:p.Gln766=
XM_005274548.3:c.2296C=	XP_005274605.1:p.Gln766=
XM_005274548.5:c.2296C=	XP_005274605.1:p.Gln766=
XM_005274550.3:c.2296C=	XP_005274607.1:p.Gln766=
XM_005274550.5:c.2296C=	XP_005274607.1:p.Gln766=
XM_006724496.2:c.2296C=	XP_006724559.1:p.Gln766=
XM_006724496.4:c.2296C=	XP_006724559.1:p.Gln766=
XM_006724498.2:c.1750C=	XP_006724561.1:p.Gln584=
XM_006724498.4:c.1750C=	XP_006724561.1:p.Gln584=
XM_011545537.1:c.2197C=	XP_011543839.1:p.Gln733=
XM_011545537.3:c.2197C=	XP_011543839.1:p.Gln733=
XM_011545538.1:c.1279C=	XP_011543840.1:p.Gln427=
XM_011545538.3:c.1279C=	XP_011543840.1:p.Gln427=
XM_017029580.2:c.1390C=	XP_016885069.1:p.Gln464=
XR_001755697.2:n.2466C=
XR_001755698.2:n.2466C=
XR_002958777.1:n.2466C=
XR_950461.1:n.2480C=
XR_950461.3:n.2466C=