Canonical Allele Identifier: CA2216730774

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30755961A= , CM000678.2:g.30755961A=	GRCh38
NC_000016.9:g.30767282A= , CM000678.1:g.30767282A=	GRCh37
NC_000016.8:g.30674783A=	NCBI36
NG_016616.1:g.12663A=
NG_016616.2:g.12663A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.557-221A= MANE Select	ENSP00000455607.1:n.557-221A=
ENST00000328273.11:c.557-221A=	ENSP00000329968.7:n.557-221A=
ENST00000424889.7:c.557-221A=	ENSP00000388571.3:n.557-221A=
ENST00000563588.5:c.557-221A=	ENSP00000455607.1:n.557-221A=
ENST00000563913.5:n.890-221A=
ENST00000564838.5:n.931-629A=
ENST00000565897.5:c.557-221A=	ENSP00000457359.1:n.557-221A=
ENST00000565924.5:c.557-221A=	ENSP00000455091.1:n.557-221A=
ENST00000569684.1:n.969-221A=
NM_000294.2:c.557-221A=	NP_000285.1:n.557-221A=
NM_001172432.1:c.557-221A=	NP_001165903.1:n.557-221A=
NM_000294.3:c.557-221A= MANE Select	NP_000285.1:n.557-221A=
NM_001172432.2:c.557-221A=	NP_001165903.1:n.557-221A=