Canonical Allele Identifier: CA2216725077

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753190_30753191delinsAC , CM000678.2:g.30753190_30753191delinsAC	GRCh38
NC_000016.9:g.30764511_30764512delinsAC , CM000678.1:g.30764511_30764512delinsAC	GRCh37
NC_000016.8:g.30672012_30672013delinsAC	NCBI36
NG_016616.1:g.9892_9893delinsAC
NG_016616.2:g.9892_9893delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000563588.6:c.327-42_327-41delinsAC MANE Select	ENSP00000455607.1:n.327-42_327-41delinsAC
ENST00000328273.11:c.327-42_327-41delinsAC	ENSP00000329968.7:n.327-42_327-41delinsAC
ENST00000424889.7:c.327-42_327-41delinsAC	ENSP00000388571.3:n.327-42_327-41delinsAC
ENST00000563588.5:c.327-42_327-41delinsAC	ENSP00000455607.1:n.327-42_327-41delinsAC
ENST00000563607.1:c.263-42_263-41delinsAC	ENSP00000454641.1:n.263-42_263-41delinsAC
ENST00000563913.5:n.660-42_660-41delinsAC
ENST00000564838.5:n.701-42_701-41delinsAC
ENST00000565897.5:c.327-42_327-41delinsAC	ENSP00000457359.1:n.327-42_327-41delinsAC
ENST00000565924.5:c.327-42_327-41delinsAC	ENSP00000455091.1:n.327-42_327-41delinsAC
ENST00000569684.1:n.697_698delinsAC
NM_000294.2:c.327-42_327-41delinsAC	NP_000285.1:n.327-42_327-41delinsAC
NM_001172432.1:c.327-42_327-41delinsAC	NP_001165903.1:n.327-42_327-41delinsAC
NM_000294.3:c.327-42_327-41delinsAC MANE Select	NP_000285.1:n.327-42_327-41delinsAC
NM_001172432.2:c.327-42_327-41delinsAC	NP_001165903.1:n.327-42_327-41delinsAC