Canonical Allele Identifier: CA2220394989

Gene: PHKB

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47596425T= , CM000678.2:g.47596425T=	GRCh38
NC_000016.9:g.47630336T= , CM000678.1:g.47630336T=	GRCh37
NC_000016.8:g.46187837T=	NCBI36
NG_016598.1:g.140127T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000293.3:c.1257T= MANE Select	NP_000284.1:p.Tyr419=
ENST00000323584.10:c.1257T= MANE Select	ENSP00000313504.5:p.Tyr419=
NM_000293.2:c.1257T=	NP_000284.1:p.Tyr419=
NM_001031835.2:c.1236T=	NP_001027005.1:p.Tyr412=
NM_001031835.3:c.1236T=	NP_001027005.1:p.Tyr412=
NM_001363837.1:c.1257T=	NP_001350766.1:p.Tyr419=
ENST00000299167.12:c.1257T=	ENSP00000299167.8:p.Tyr419=
ENST00000323584.9:c.1257T=	ENSP00000313504.5:p.Tyr419=
ENST00000566044.5:c.1236T=	ENSP00000456729.1:p.Tyr412=
ENST00000566436.1:n.118T=
ENST00000696809.1:c.1236T=	ENSP00000512887.1:p.Tyr412=
ENST00000699276.1:c.1236T=	ENSP00000514257.1:p.Tyr412=
XM_005255983.3:c.1257T=	XP_005256040.1:p.Tyr419=
XM_005255983.4:c.1257T=	XP_005256040.1:p.Tyr419=
XM_005255984.3:c.1236T=	XP_005256041.1:p.Tyr412=
XM_005255984.4:c.1236T=	XP_005256041.1:p.Tyr412=
XM_011523106.1:c.1257T=	XP_011521408.1:p.Tyr419=
XM_017023282.1:c.144T=	XP_016878771.1:p.Tyr48=
XM_017023283.1:c.-249T=	XP_016878772.1:n.-249T=
XM_017023284.1:c.-249T=	XP_016878773.1:n.-249T=
XR_001751913.1:n.1272T=