Canonical Allele Identifier: CA2216725761

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753423T= , CM000678.2:g.30753423T=	GRCh38
NC_000016.9:g.30764744T= , CM000678.1:g.30764744T=	GRCh37
NC_000016.8:g.30672245T=	NCBI36
NG_016616.1:g.10125T=
NG_016616.2:g.10125T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.422T= MANE Select	ENSP00000455607.1:p.Val141=
ENST00000328273.11:c.422T=	ENSP00000329968.7:p.Val141=
ENST00000424889.7:c.422T=	ENSP00000388571.3:p.Val141=
ENST00000561712.1:c.96T=
ENST00000563588.5:c.422T=	ENSP00000455607.1:p.Val141=
ENST00000563607.1:c.*94T=	ENSP00000454641.1:n.*94T=
ENST00000563913.5:n.755T=
ENST00000564838.5:n.796T=
ENST00000565897.5:c.422T=	ENSP00000457359.1:p.Val141=
ENST00000565924.5:c.422T=	ENSP00000455091.1:p.Val141=
ENST00000569684.1:n.834T=
NM_000294.2:c.422T=	NP_000285.1:p.Val141=
NM_001172432.1:c.422T=	NP_001165903.1:p.Val141=
NM_000294.3:c.422T= MANE Select	NP_000285.1:p.Val141=
NM_001172432.2:c.422T=	NP_001165903.1:p.Val141=