Canonical Allele Identifier: CA2216731507

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756363C= , CM000678.2:g.30756363C=	GRCh38
NC_000016.9:g.30767684C= , CM000678.1:g.30767684C=	GRCh37
NC_000016.8:g.30675185C=	NCBI36
NG_016616.1:g.13065C=
NG_016616.2:g.13065C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.648-4C= MANE Select	ENSP00000455607.1:n.648-4C=
ENST00000328273.11:c.656C=	ENSP00000329968.7:p.Pro219=
ENST00000424889.7:c.648-4C=	ENSP00000388571.3:n.648-4C=
ENST00000563588.5:c.648-4C=	ENSP00000455607.1:n.648-4C=
ENST00000563913.5:n.981-4C=
ENST00000564838.5:n.931-227C=
ENST00000565897.5:c.648-4C=	ENSP00000457359.1:n.648-4C=
ENST00000565924.5:c.648-4C=	ENSP00000455091.1:n.648-4C=
ENST00000569684.1:n.1068C=
NM_000294.2:c.648-4C=	NP_000285.1:n.648-4C=
NM_001172432.1:c.648-4C=	NP_001165903.1:n.648-4C=
NM_000294.3:c.648-4C= MANE Select	NP_000285.1:n.648-4C=
NM_001172432.2:c.648-4C=	NP_001165903.1:n.648-4C=