Canonical Allele Identifier: CA2216719969

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30751179G= , CM000678.2:g.30751179G=	GRCh38
NC_000016.9:g.30762500G= , CM000678.1:g.30762500G=	GRCh37
NC_000016.8:g.30670001G=	NCBI36
NG_016616.1:g.7881G=
NG_016616.2:g.7881G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000294.3:c.169G= MANE Select	NP_000285.1:p.Val57=
ENST00000563588.6:c.169G= MANE Select	ENSP00000455607.1:p.Val57=
NM_000294.2:c.169G=	NP_000285.1:p.Val57=
NM_001172432.1:c.169G=	NP_001165903.1:p.Val57=
NM_001172432.2:c.169G=	NP_001165903.1:p.Val57=
ENST00000328273.11:c.169G=	ENSP00000329968.7:p.Val57=
ENST00000424889.7:c.169G=	ENSP00000388571.3:p.Val57=
ENST00000563588.5:c.169G=	ENSP00000455607.1:p.Val57=
ENST00000563607.1:c.169G=	ENSP00000454641.1:p.Val57=
ENST00000563913.5:n.235G=
ENST00000564838.5:n.276G=
ENST00000565897.5:c.169G=	ENSP00000457359.1:p.Val57=
ENST00000565924.5:c.169G=	ENSP00000455091.1:p.Val57=
ENST00000569762.1:n.146G=