Canonical Allele Identifier: CA2216731786

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756475C= , CM000678.2:g.30756475C=	GRCh38
NC_000016.9:g.30767796C= , CM000678.1:g.30767796C=	GRCh37
NC_000016.8:g.30675297C=	NCBI36
NG_016616.1:g.13177C=
NG_016616.2:g.13177C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000563588.6:c.756C= MANE Select	ENSP00000455607.1:p.Phe252=
ENST00000328273.11:c.768C=	ENSP00000329968.7:p.Phe256=
ENST00000424889.7:c.756C=	ENSP00000388571.3:p.Phe252=
ENST00000563588.5:c.756C=	ENSP00000455607.1:p.Phe252=
ENST00000563913.5:n.1089C=
ENST00000564838.5:n.931-115C=
ENST00000565897.5:c.756C=	ENSP00000457359.1:p.Phe252=
ENST00000565924.5:c.756C=	ENSP00000455091.1:p.Phe252=
NM_000294.2:c.756C=	NP_000285.1:p.Phe252=
NM_001172432.1:c.756C=	NP_001165903.1:p.Phe252=
NM_000294.3:c.756C= MANE Select	NP_000285.1:p.Phe252=
NM_001172432.2:c.756C=	NP_001165903.1:p.Phe252=