Canonical Allele Identifier: CA494684050

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30751553C>T , CM000678.2:g.30751553C>T	GRCh38
NC_000016.9:g.30762874C>T , CM000678.1:g.30762874C>T	GRCh37
NC_000016.8:g.30670375C>T	NCBI36
NG_016616.1:g.8255C>T
NG_016616.2:g.8255C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000294.3:c.276C>T MANE Select	NP_000285.1:p.Thr92=
ENST00000563588.6:c.276C>T MANE Select	ENSP00000455607.1:p.Thr92=
NM_000294.2:c.276C>T	NP_000285.1:p.Thr92=
NM_001172432.1:c.276C>T	NP_001165903.1:p.Thr92=
NM_001172432.2:c.276C>T	NP_001165903.1:p.Thr92=
ENST00000328273.11:c.276C>T	ENSP00000329968.7:p.Thr92=
ENST00000424889.7:c.276C>T	ENSP00000388571.3:p.Thr92=
ENST00000563588.5:c.276C>T	ENSP00000455607.1:p.Thr92=
ENST00000563607.1:c.212C>T	ENSP00000454641.1:p.Pro71Leu
ENST00000563913.5:n.609C>T
ENST00000564838.5:n.650C>T
ENST00000565897.5:c.276C>T	ENSP00000457359.1:p.Thr92=
ENST00000565924.5:c.276C>T	ENSP00000455091.1:p.Thr92=
ENST00000569762.1:n.520C>T