Canonical Allele Identifier: CA2216730771

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30755958_30755963delinsTCAATC , CM000678.2:g.30755958_30755963delinsTCAATC	GRCh38
NC_000016.9:g.30767279_30767284delinsTCAATC , CM000678.1:g.30767279_30767284delinsTCAATC	GRCh37
NC_000016.8:g.30674780_30674785delinsTCAATC	NCBI36
NG_016616.1:g.12660_12665delinsTCAATC
NG_016616.2:g.12660_12665delinsTCAATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.557-224_557-219delinsTCAATC MANE Select	ENSP00000455607.1:n.557-224_557-219delinsTCAATC
ENST00000328273.11:c.557-224_557-219delinsTCAATC	ENSP00000329968.7:n.557-224_557-219delinsTCAATC
ENST00000424889.7:c.557-224_557-219delinsTCAATC	ENSP00000388571.3:n.557-224_557-219delinsTCAATC
ENST00000563588.5:c.557-224_557-219delinsTCAATC	ENSP00000455607.1:n.557-224_557-219delinsTCAATC
ENST00000563913.5:n.890-224_890-219delinsTCAATC
ENST00000564838.5:n.931-632_931-627delinsTCAATC
ENST00000565897.5:c.557-224_557-219delinsTCAATC	ENSP00000457359.1:n.557-224_557-219delinsTCAATC
ENST00000565924.5:c.557-224_557-219delinsTCAATC	ENSP00000455091.1:n.557-224_557-219delinsTCAATC
ENST00000569684.1:n.969-224_969-219delinsTCAATC
NM_000294.2:c.557-224_557-219delinsTCAATC	NP_000285.1:n.557-224_557-219delinsTCAATC
NM_001172432.1:c.557-224_557-219delinsTCAATC	NP_001165903.1:n.557-224_557-219delinsTCAATC
NM_000294.3:c.557-224_557-219delinsTCAATC MANE Select	NP_000285.1:n.557-224_557-219delinsTCAATC
NM_001172432.2:c.557-224_557-219delinsTCAATC	NP_001165903.1:n.557-224_557-219delinsTCAATC