Canonical Allele Identifier: CA2216731402

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756326_30756327delinsGC , CM000678.2:g.30756326_30756327delinsGC	GRCh38
NC_000016.9:g.30767647_30767648delinsGC , CM000678.1:g.30767647_30767648delinsGC	GRCh37
NC_000016.8:g.30675148_30675149delinsGC	NCBI36
NG_016616.1:g.13028_13029delinsGC
NG_016616.2:g.13028_13029delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000563588.6:c.648-41_648-40delinsGC MANE Select	ENSP00000455607.1:n.648-41_648-40delinsGC...
ENST00000328273.11:c.648-29_648-28delinsGC	ENSP00000329968.7:n.648-29_648-28delinsGC...
ENST00000424889.7:c.648-41_648-40delinsGC	ENSP00000388571.3:n.648-41_648-40delinsGC...
ENST00000563588.5:c.648-41_648-40delinsGC	ENSP00000455607.1:n.648-41_648-40delinsGC...
ENST00000563913.5:n.981-41_981-40delinsGC
ENST00000564838.5:n.931-264_931-263delinsGC
ENST00000565897.5:c.648-41_648-40delinsGC	ENSP00000457359.1:n.648-41_648-40delinsGC...
ENST00000565924.5:c.648-41_648-40delinsGC	ENSP00000455091.1:n.648-41_648-40delinsGC...
ENST00000569684.1:n.1060-29_1060-28delinsGC
NM_000294.2:c.648-41_648-40delinsGC	NP_000285.1:n.648-41_648-40delinsGC
NM_001172432.1:c.648-41_648-40delinsGC	NP_001165903.1:n.648-41_648-40delinsGC
NM_000294.3:c.648-41_648-40delinsGC MANE Select	NP_000285.1:n.648-41_648-40delinsGC
NM_001172432.2:c.648-41_648-40delinsGC	NP_001165903.1:n.648-41_648-40delinsGC