Canonical Allele Identifier: CA2632768832

Gene: PHKG2

Linked Data

• gnomAD v4: 16-30753194-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753197del , CM000678.2:g.30753197del	GRCh38
NC_000016.9:g.30764518del , CM000678.1:g.30764518del	GRCh37
NC_000016.8:g.30672019del	NCBI36
NG_016616.1:g.9899del
NG_016616.2:g.9899del

Transcript Alleles

HGVS	Amino-acid change
ENST00000563588.6:c.327-35del MANE Select	ENSP00000455607.1:n.327-35del
ENST00000328273.11:c.327-35del	ENSP00000329968.7:n.327-35del
ENST00000424889.7:c.327-35del	ENSP00000388571.3:n.327-35del
ENST00000563588.5:c.327-35del	ENSP00000455607.1:n.327-35del
ENST00000563607.1:c.263-35del	ENSP00000454641.1:n.263-35del
ENST00000563913.5:n.660-35del
ENST00000564838.5:n.701-35del
ENST00000565897.5:c.327-35del	ENSP00000457359.1:n.327-35del
ENST00000565924.5:c.327-35del	ENSP00000455091.1:n.327-35del
ENST00000569684.1:n.704del
NM_000294.2:c.327-35del	NP_000285.1:n.327-35del
NM_001172432.1:c.327-35del	NP_001165903.1:n.327-35del
NM_000294.3:c.327-35del MANE Select	NP_000285.1:n.327-35del
NM_001172432.2:c.327-35del	NP_001165903.1:n.327-35del