Canonical Allele Identifier: CA2575971692

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756129del , CM000678.2:g.30756129del	GRCh38
NC_000016.9:g.30767450del , CM000678.1:g.30767450del	GRCh37
NC_000016.8:g.30674951del	NCBI36
NG_016616.1:g.12831del
NG_016616.2:g.12831del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.557-53del MANE Select	ENSP00000455607.1:n.557-53del
ENST00000328273.11:c.557-53del	ENSP00000329968.7:n.557-53del
ENST00000424889.7:c.557-53del	ENSP00000388571.3:n.557-53del
ENST00000563588.5:c.557-53del	ENSP00000455607.1:n.557-53del
ENST00000563913.5:n.890-53del
ENST00000564838.5:n.931-461del
ENST00000565897.5:c.557-53del	ENSP00000457359.1:n.557-53del
ENST00000565924.5:c.557-53del	ENSP00000455091.1:n.557-53del
ENST00000569684.1:n.969-53del
NM_000294.2:c.557-53del	NP_000285.1:n.557-53del
NM_001172432.1:c.557-53del	NP_001165903.1:n.557-53del
NM_000294.3:c.557-53del MANE Select	NP_000285.1:n.557-53del
NM_001172432.2:c.557-53del	NP_001165903.1:n.557-53del