Canonical Allele Identifier: CA2216725842

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753449G= , CM000678.2:g.30753449G=	GRCh38
NC_000016.9:g.30764770G= , CM000678.1:g.30764770G=	GRCh37
NC_000016.8:g.30672271G=	NCBI36
NG_016616.1:g.10151G=
NG_016616.2:g.10151G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.448G= MANE Select	ENSP00000455607.1:p.Val150=
ENST00000328273.11:c.448G=	ENSP00000329968.7:p.Val150=
ENST00000424889.7:c.448G=	ENSP00000388571.3:p.Val150=
ENST00000561712.1:c.122G=
ENST00000563588.5:c.448G=	ENSP00000455607.1:p.Val150=
ENST00000563607.1:c.*120G=	ENSP00000454641.1:n.*120G=
ENST00000563913.5:n.781G=
ENST00000564838.5:n.822G=
ENST00000565897.5:c.448G=	ENSP00000457359.1:p.Val150=
ENST00000565924.5:c.448G=	ENSP00000455091.1:p.Val150=
ENST00000569684.1:n.860G=
NM_000294.2:c.448G=	NP_000285.1:p.Val150=
NM_001172432.1:c.448G=	NP_001165903.1:p.Val150=
NM_000294.3:c.448G= MANE Select	NP_000285.1:p.Val150=
NM_001172432.2:c.448G=	NP_001165903.1:p.Val150=