Canonical Allele Identifier: CA2216731870

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756497C= , CM000678.2:g.30756497C=	GRCh38
NC_000016.9:g.30767818C= , CM000678.1:g.30767818C=	GRCh37
NC_000016.8:g.30675319C=	NCBI36
NG_016616.1:g.13199C=
NG_016616.2:g.13199C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.778C= MANE Select	ENSP00000455607.1:p.Arg260=
ENST00000328273.11:c.790C=	ENSP00000329968.7:p.Arg264=
ENST00000424889.7:c.778C=	ENSP00000388571.3:p.Arg260=
ENST00000563588.5:c.778C=	ENSP00000455607.1:p.Arg260=
ENST00000563913.5:n.1111C=
ENST00000564838.5:n.931-93C=
ENST00000565897.5:c.778C=	ENSP00000457359.1:p.Arg260=
NM_000294.2:c.778C=	NP_000285.1:p.Arg260=
NM_001172432.1:c.778C=	NP_001165903.1:p.Arg260=
NM_000294.3:c.778C= MANE Select	NP_000285.1:p.Arg260=
NM_001172432.2:c.778C=	NP_001165903.1:p.Arg260=