Canonical Allele Identifier: CA2216725059

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753178T= , CM000678.2:g.30753178T=	GRCh38
NC_000016.9:g.30764499T= , CM000678.1:g.30764499T=	GRCh37
NC_000016.8:g.30672000T=	NCBI36
NG_016616.1:g.9880T=
NG_016616.2:g.9880T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000563588.6:c.327-54T= MANE Select	ENSP00000455607.1:n.327-54T=
ENST00000328273.11:c.327-54T=	ENSP00000329968.7:n.327-54T=
ENST00000424889.7:c.327-54T=	ENSP00000388571.3:n.327-54T=
ENST00000563588.5:c.327-54T=	ENSP00000455607.1:n.327-54T=
ENST00000563607.1:c.263-54T=	ENSP00000454641.1:n.263-54T=
ENST00000563913.5:n.660-54T=
ENST00000564838.5:n.701-54T=
ENST00000565897.5:c.327-54T=	ENSP00000457359.1:n.327-54T=
ENST00000565924.5:c.327-54T=	ENSP00000455091.1:n.327-54T=
ENST00000569684.1:n.685T=
NM_000294.2:c.327-54T=	NP_000285.1:n.327-54T=
NM_001172432.1:c.327-54T=	NP_001165903.1:n.327-54T=
NM_000294.3:c.327-54T= MANE Select	NP_000285.1:n.327-54T=
NM_001172432.2:c.327-54T=	NP_001165903.1:n.327-54T=