Canonical Allele Identifier: CA8013102

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30751537C>G , CM000678.2:g.30751537C>G	GRCh38
NC_000016.9:g.30762858C>G , CM000678.1:g.30762858C>G	GRCh37
NC_000016.8:g.30670359C>G	NCBI36
NG_016616.1:g.8239C>G
NG_016616.2:g.8239C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000294.3:c.272-12C>G MANE Select	NP_000285.1:n.272-12C>G
ENST00000563588.6:c.272-12C>G MANE Select	ENSP00000455607.1:n.272-12C>G
NM_000294.2:c.272-12C>G	NP_000285.1:n.272-12C>G
NM_001172432.1:c.272-12C>G	NP_001165903.1:n.272-12C>G
NM_001172432.2:c.272-12C>G	NP_001165903.1:n.272-12C>G
ENST00000328273.11:c.272-12C>G	ENSP00000329968.7:n.272-12C>G
ENST00000424889.7:c.272-12C>G	ENSP00000388571.3:n.272-12C>G
ENST00000563588.5:c.272-12C>G	ENSP00000455607.1:n.272-12C>G
ENST00000563607.1:c.208-12C>G	ENSP00000454641.1:n.208-12C>G
ENST00000563913.5:n.593C>G
ENST00000564838.5:n.634C>G
ENST00000565897.5:c.272-12C>G	ENSP00000457359.1:n.272-12C>G
ENST00000565924.5:c.272-12C>G	ENSP00000455091.1:n.272-12C>G
ENST00000569762.1:n.504C>G