Canonical Allele Identifier: CA2216726217

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753616G= , CM000678.2:g.30753616G=	GRCh38
NC_000016.9:g.30764937G= , CM000678.1:g.30764937G=	GRCh37
NC_000016.8:g.30672438G=	NCBI36
NG_016616.1:g.10318G=
NG_016616.2:g.10318G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.556+59G= MANE Select	ENSP00000455607.1:n.556+59G=
ENST00000328273.11:c.556+59G=	ENSP00000329968.7:n.556+59G=
ENST00000424889.7:c.556+59G=	ENSP00000388571.3:n.556+59G=
ENST00000561712.1:c.230+59G=
ENST00000563588.5:c.556+59G=	ENSP00000455607.1:n.556+59G=
ENST00000563913.5:n.889+59G=
ENST00000564838.5:n.930+59G=
ENST00000565897.5:c.556+59G=	ENSP00000457359.1:n.556+59G=
ENST00000565924.5:c.556+59G=	ENSP00000455091.1:n.556+59G=
ENST00000569684.1:n.968+59G=
NM_000294.2:c.556+59G=	NP_000285.1:n.556+59G=
NM_001172432.1:c.556+59G=	NP_001165903.1:n.556+59G=
NM_000294.3:c.556+59G= MANE Select	NP_000285.1:n.556+59G=
NM_001172432.2:c.556+59G=	NP_001165903.1:n.556+59G=