Canonical Allele Identifier: CA2216731825

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756482C= , CM000678.2:g.30756482C=	GRCh38
NC_000016.9:g.30767803C= , CM000678.1:g.30767803C=	GRCh37
NC_000016.8:g.30675304C=	NCBI36
NG_016616.1:g.13184C=
NG_016616.2:g.13184C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000563588.6:c.763C= MANE Select	ENSP00000455607.1:p.Pro255=
ENST00000328273.11:c.775C=	ENSP00000329968.7:p.Pro259=
ENST00000424889.7:c.763C=	ENSP00000388571.3:p.Pro255=
ENST00000563588.5:c.763C=	ENSP00000455607.1:p.Pro255=
ENST00000563913.5:n.1096C=
ENST00000564838.5:n.931-108C=
ENST00000565897.5:c.763C=	ENSP00000457359.1:p.Pro255=
ENST00000565924.5:c.763C=
NM_000294.2:c.763C=	NP_000285.1:p.Pro255=
NM_001172432.1:c.763C=	NP_001165903.1:p.Pro255=
NM_000294.3:c.763C= MANE Select	NP_000285.1:p.Pro255=
NM_001172432.2:c.763C=	NP_001165903.1:p.Pro255=