Canonical Allele Identifier: CA2216731373

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756311T= , CM000678.2:g.30756311T=	GRCh38
NC_000016.9:g.30767632T= , CM000678.1:g.30767632T=	GRCh37
NC_000016.8:g.30675133T=	NCBI36
NG_016616.1:g.13013T=
NG_016616.2:g.13013T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.647+39T= MANE Select	ENSP00000455607.1:n.647+39T=
ENST00000328273.11:c.647+39T=	ENSP00000329968.7:n.647+39T=
ENST00000424889.7:c.647+39T=	ENSP00000388571.3:n.647+39T=
ENST00000563588.5:c.647+39T=	ENSP00000455607.1:n.647+39T=
ENST00000563913.5:n.980+39T=
ENST00000564838.5:n.931-279T=
ENST00000565897.5:c.647+39T=	ENSP00000457359.1:n.647+39T=
ENST00000565924.5:c.647+39T=	ENSP00000455091.1:n.647+39T=
ENST00000569684.1:n.1059+39T=
NM_000294.2:c.647+39T=	NP_000285.1:n.647+39T=
NM_001172432.1:c.647+39T=	NP_001165903.1:n.647+39T=
NM_000294.3:c.647+39T= MANE Select	NP_000285.1:n.647+39T=
NM_001172432.2:c.647+39T=	NP_001165903.1:n.647+39T=