Canonical Allele Identifier: CA2216732070

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756574T= , CM000678.2:g.30756574T=	GRCh38
NC_000016.9:g.30767895T= , CM000678.1:g.30767895T=	GRCh37
NC_000016.8:g.30675396T=	NCBI36
NG_016616.1:g.13276T=
NG_016616.2:g.13276T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.802-16T= MANE Select	ENSP00000455607.1:n.802-16T=
ENST00000328273.11:c.814-16T=	ENSP00000329968.7:n.814-16T=
ENST00000424889.7:c.802-16T=	ENSP00000388571.3:n.802-16T=
ENST00000563588.5:c.802-16T=	ENSP00000455607.1:n.802-16T=
ENST00000563913.5:n.1135-16T=
ENST00000564838.5:n.931-16T=
NM_000294.2:c.802-16T=	NP_000285.1:n.802-16T=
NM_001172432.1:c.802-16T=	NP_001165903.1:n.802-16T=
NM_000294.3:c.802-16T= MANE Select	NP_000285.1:n.802-16T=
NM_001172432.2:c.802-16T=	NP_001165903.1:n.802-16T=