Canonical Allele Identifier: CA1806686068

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231893_102231897delinsGAAAA , CM000670.2:g.102231893_102231897delinsGAAAA	GRCh38
NC_000008.10:g.103244121_103244125delinsGAAAA , CM000670.1:g.103244121_103244125delinsGAAAA	GRCh37
NC_000008.9:g.103313297_103313301delinsGAAAA	NCBI36
NG_016617.1:g.12222_12226delinsTTTTC , LRG_788:g.12222_12226delinsTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+252_204+256delinsTTTTC MANE Select	ENSP00000251810.3:n.204+252_204+256delinsTTTTC
ENST00000251810.7:c.204+252_204+256delinsTTTTC	ENSP00000251810.3:n.204+252_204+256delinsTTTTC
ENST00000395912.6:c.49-5863_49-5859delinsTTTTC	ENSP00000379248.2:n.49-5863_49-5859delinsTTTTC
ENST00000517517.1:n.513+252_513+256delinsTTTTC
ENST00000519317.5:c.48+6930_48+6934delinsTTTTC	ENSP00000430641.1:n.48+6930_48+6934delinsTTTTC
ENST00000519962.5:c.48+6930_48+6934delinsTTTTC	ENSP00000429140.1:n.48+6930_48+6934delinsTTTTC
ENST00000522368.5:c.373+252_373+256delinsTTTTC
ENST00000522394.1:c.122+334_122+338delinsTTTTC	ENSP00000429578.1:n.122+334_122+338delinsTTTTC
ENST00000523957.1:c.*127+252_*127+256delinsTTTTC	ENSP00000427830.1:n.*127+252_*127+256delinsTTTTC
ENST00000621845.1:c.42+252_42+256delinsTTTTC	ENSP00000484318.1:n.42+252_42+256delinsTTTTC
NM_001172477.1:c.420+252_420+256delinsTTTTC , LRG_788t1:c.420+252_420+256delinsTTTTC	NP_001165948.1:n.420+252_420+256delinsTTTTC
NM_001172478.1:c.49-5863_49-5859delinsTTTTC	NP_001165949.1:n.49-5863_49-5859delinsTTTTC
NM_015713.4:c.204+252_204+256delinsTTTTC , LRG_788t2:c.204+252_204+256delinsTTTTC	NP_056528.2:n.204+252_204+256delinsTTTTC
NM_001172478.2:c.49-5863_49-5859delinsTTTTC	NP_001165949.1:n.49-5863_49-5859delinsTTTTC
NM_015713.5:c.204+252_204+256delinsTTTTC MANE Select	NP_056528.2:n.204+252_204+256delinsTTTTC