Canonical Allele Identifier: CA2216725385

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753275G= , CM000678.2:g.30753275G=	GRCh38
NC_000016.9:g.30764596G= , CM000678.1:g.30764596G=	GRCh37
NC_000016.8:g.30672097G=	NCBI36
NG_016616.1:g.9977G=
NG_016616.2:g.9977G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.370G= MANE Select	ENSP00000455607.1:p.Ala124=
ENST00000328273.11:c.370G=	ENSP00000329968.7:p.Ala124=
ENST00000424889.7:c.370G=	ENSP00000388571.3:p.Ala124=
ENST00000561712.1:c.44G=
ENST00000563588.5:c.370G=	ENSP00000455607.1:p.Ala124=
ENST00000563607.1:c.*42G=	ENSP00000454641.1:n.*42G=
ENST00000563913.5:n.703G=
ENST00000564838.5:n.744G=
ENST00000565897.5:c.370G=	ENSP00000457359.1:p.Ala124=
ENST00000565924.5:c.370G=	ENSP00000455091.1:p.Ala124=
ENST00000569684.1:n.782G=
NM_000294.2:c.370G=	NP_000285.1:p.Ala124=
NM_001172432.1:c.370G=	NP_001165903.1:p.Ala124=
NM_000294.3:c.370G= MANE Select	NP_000285.1:p.Ala124=
NM_001172432.2:c.370G=	NP_001165903.1:p.Ala124=