Canonical Allele Identifier: CA2418091458

Gene: PHKA2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18951165G= , CM000685.2:g.18951165G=	GRCh38
NC_000023.10:g.18969283G= , CM000685.1:g.18969283G=	GRCh37
NC_000023.9:g.18879204G=	NCBI36
NG_016622.1:g.38198C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379942.5:c.393C= MANE Select	ENSP00000369274.4:p.Gly131=
ENST00000379942.4:c.393C=	ENSP00000369274.4:p.Gly131=
NM_000292.2:c.393C=	NP_000283.1:p.Gly131=
XM_005274548.3:c.393C=	XP_005274605.1:p.Gly131=
XM_005274550.3:c.393C=	XP_005274607.1:p.Gly131=
XM_006724496.2:c.393C=	XP_006724559.1:p.Gly131=
XM_006724498.2:c.-93+1329C=	XP_006724561.1:n.-93+1329C=
XM_011545537.1:c.393C=	XP_011543839.1:p.Gly131=
XR_950461.1:n.577C=
XM_005274548.5:c.393C=	XP_005274605.1:p.Gly131=
XM_005274550.5:c.393C=	XP_005274607.1:p.Gly131=
XM_006724496.4:c.393C=	XP_006724559.1:p.Gly131=
XM_006724498.4:c.-93+1329C=	XP_006724561.1:n.-93+1329C=
XM_011545537.3:c.393C=	XP_011543839.1:p.Gly131=
XM_017029580.2:c.-449C=	XP_016885069.1:n.-449C=
XR_001755697.2:n.563C=
XR_001755698.2:n.563C=
XR_002958777.1:n.563C=
XR_950461.3:n.563C=
NM_000292.3:c.393C= MANE Select	NP_000283.1:p.Gly131=