Canonical Allele Identifier: CA2216719992

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30751185G= , CM000678.2:g.30751185G=	GRCh38
NC_000016.9:g.30762506G= , CM000678.1:g.30762506G=	GRCh37
NC_000016.8:g.30670007G=	NCBI36
NG_016616.1:g.7887G=
NG_016616.2:g.7887G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000294.3:c.175G= MANE Select	NP_000285.1:p.Ala59=
ENST00000563588.6:c.175G= MANE Select	ENSP00000455607.1:p.Ala59=
NM_000294.2:c.175G=	NP_000285.1:p.Ala59=
NM_001172432.1:c.175G=	NP_001165903.1:p.Ala59=
NM_001172432.2:c.175G=	NP_001165903.1:p.Ala59=
ENST00000328273.11:c.175G=	ENSP00000329968.7:p.Ala59=
ENST00000424889.7:c.175G=	ENSP00000388571.3:p.Ala59=
ENST00000563588.5:c.175G=	ENSP00000455607.1:p.Ala59=
ENST00000563607.1:c.175G=	ENSP00000454641.1:p.Ala59=
ENST00000563913.5:n.241G=
ENST00000564838.5:n.282G=
ENST00000565897.5:c.175G=	ENSP00000457359.1:p.Ala59=
ENST00000565924.5:c.175G=	ENSP00000455091.1:p.Ala59=
ENST00000569762.1:n.152G=