Canonical Allele Identifier: CA2216731385

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756316T= , CM000678.2:g.30756316T=	GRCh38
NC_000016.9:g.30767637T= , CM000678.1:g.30767637T=	GRCh37
NC_000016.8:g.30675138T=	NCBI36
NG_016616.1:g.13018T=
NG_016616.2:g.13018T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000563588.6:c.647+44T= MANE Select	ENSP00000455607.1:n.647+44T=
ENST00000328273.11:c.648-39T=	ENSP00000329968.7:n.648-39T=
ENST00000424889.7:c.647+44T=	ENSP00000388571.3:n.647+44T=
ENST00000563588.5:c.647+44T=	ENSP00000455607.1:n.647+44T=
ENST00000563913.5:n.980+44T=
ENST00000564838.5:n.931-274T=
ENST00000565897.5:c.647+44T=	ENSP00000457359.1:n.647+44T=
ENST00000565924.5:c.647+44T=	ENSP00000455091.1:n.647+44T=
ENST00000569684.1:n.1060-39T=
NM_000294.2:c.647+44T=	NP_000285.1:n.647+44T=
NM_001172432.1:c.647+44T=	NP_001165903.1:n.647+44T=
NM_000294.3:c.647+44T= MANE Select	NP_000285.1:n.647+44T=
NM_001172432.2:c.647+44T=	NP_001165903.1:n.647+44T=