Canonical Allele Identifier: CA2418091456

Gene: PHKA2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.18951163T= , CM000685.2:g.18951163T=	GRCh38
NC_000023.10:g.18969281T= , CM000685.1:g.18969281T=	GRCh37
NC_000023.9:g.18879202T=	NCBI36
NG_016622.1:g.38200A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000292.3:c.395A= MANE Select	NP_000283.1:p.His132=
ENST00000379942.5:c.395A= MANE Select	ENSP00000369274.4:p.His132=
NM_000292.2:c.395A=	NP_000283.1:p.His132=
ENST00000379942.4:c.395A=	ENSP00000369274.4:p.His132=
XM_005274548.3:c.395A=	XP_005274605.1:p.His132=
XM_005274548.5:c.395A=	XP_005274605.1:p.His132=
XM_005274550.3:c.395A=	XP_005274607.1:p.His132=
XM_005274550.5:c.395A=	XP_005274607.1:p.His132=
XM_006724496.2:c.395A=	XP_006724559.1:p.His132=
XM_006724496.4:c.395A=	XP_006724559.1:p.His132=
XM_006724498.2:c.-93+1331A=	XP_006724561.1:n.-93+1331A=
XM_006724498.4:c.-93+1331A=	XP_006724561.1:n.-93+1331A=
XM_011545537.1:c.395A=	XP_011543839.1:p.His132=
XM_011545537.3:c.395A=	XP_011543839.1:p.His132=
XM_017029580.2:c.-447A=	XP_016885069.1:n.-447A=
XR_001755697.2:n.565A=
XR_001755698.2:n.565A=
XR_002958777.1:n.565A=
XR_950461.1:n.579A=
XR_950461.3:n.565A=