Canonical Allele Identifier: CA494683707

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30751187T>C , CM000678.2:g.30751187T>C	GRCh38
NC_000016.9:g.30762508T>C , CM000678.1:g.30762508T>C	GRCh37
NC_000016.8:g.30670009T>C	NCBI36
NG_016616.1:g.7889T>C
NG_016616.2:g.7889T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000294.3:c.177T>C MANE Select	NP_000285.1:p.Ala59=
ENST00000563588.6:c.177T>C MANE Select	ENSP00000455607.1:p.Ala59=
NM_000294.2:c.177T>C	NP_000285.1:p.Ala59=
NM_001172432.1:c.177T>C	NP_001165903.1:p.Ala59=
NM_001172432.2:c.177T>C	NP_001165903.1:p.Ala59=
ENST00000328273.11:c.177T>C	ENSP00000329968.7:p.Ala59=
ENST00000424889.7:c.177T>C	ENSP00000388571.3:p.Ala59=
ENST00000563588.5:c.177T>C	ENSP00000455607.1:p.Ala59=
ENST00000563607.1:c.177T>C	ENSP00000454641.1:p.Ala59=
ENST00000563913.5:n.243T>C
ENST00000564838.5:n.284T>C
ENST00000565897.5:c.177T>C	ENSP00000457359.1:p.Ala59=
ENST00000565924.5:c.177T>C	ENSP00000455091.1:p.Ala59=
ENST00000569762.1:n.154T>C