Canonical Allele Identifier: CA2220492734

Gene: PHKB

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47696487A= , CM000678.2:g.47696487A=	GRCh38
NC_000016.9:g.47730398A= , CM000678.1:g.47730398A=	GRCh37
NC_000016.8:g.46287899A=	NCBI36
NG_016598.1:g.240189A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696809.1:c.*1576A=	ENSP00000512887.1:n.*1576A=
ENST00000699276.1:c.*630A=	ENSP00000514257.1:n.*630A=
ENST00000323584.10:c.3002A= MANE Select	ENSP00000313504.5:p.Glu1001=
ENST00000299167.12:c.3002A=	ENSP00000299167.8:p.Glu1001=
ENST00000323584.9:c.3002A=	ENSP00000313504.5:p.Glu1001=
ENST00000564711.2:c.16A=
ENST00000566044.5:c.2981A=	ENSP00000456729.1:p.Glu994=
ENST00000566319.2:n.1818A=
NM_000293.2:c.3002A=	NP_000284.1:p.Glu1001=
NM_001031835.2:c.2981A=	NP_001027005.1:p.Glu994=
XM_005255983.3:c.3002A=	XP_005256040.1:p.Glu1001=
XM_005255984.3:c.2981A=	XP_005256041.1:p.Glu994=
XM_011523107.1:c.1580A=	XP_011521409.1:p.Glu527=
NM_001363837.1:c.3002A=	NP_001350766.1:p.Glu1001=
XM_005255983.4:c.3002A=	XP_005256040.1:p.Glu1001=
XM_005255984.4:c.2981A=	XP_005256041.1:p.Glu994=
XM_017023282.1:c.1889A=	XP_016878771.1:p.Glu630=
XM_017023283.1:c.1580A=	XP_016878772.1:p.Glu527=
XM_017023284.1:c.1580A=	XP_016878773.1:p.Glu527=
XR_001751913.1:n.2926A=
NM_000293.3:c.3002A= MANE Select	NP_000284.1:p.Glu1001=
NM_001031835.3:c.2981A=	NP_001027005.1:p.Glu994=