Canonical Allele Identifier: CA1806686061

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231886_102231887delinsAG , CM000670.2:g.102231886_102231887delinsAG	GRCh38
NC_000008.10:g.103244114_103244115delinsAG , CM000670.1:g.103244114_103244115delinsAG	GRCh37
NC_000008.9:g.103313290_103313291delinsAG	NCBI36
NG_016617.1:g.12232_12233delinsCT , LRG_788:g.12232_12233delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+262_204+263delinsCT MANE Select	ENSP00000251810.3:n.204+262_204+263delinsCT
ENST00000251810.7:c.204+262_204+263delinsCT	ENSP00000251810.3:n.204+262_204+263delinsCT
ENST00000395912.6:c.49-5853_49-5852delinsCT	ENSP00000379248.2:n.49-5853_49-5852delinsCT
ENST00000517517.1:n.513+262_513+263delinsCT
ENST00000519317.5:c.48+6940_48+6941delinsCT	ENSP00000430641.1:n.48+6940_48+6941delinsCT
ENST00000519962.5:c.48+6940_48+6941delinsCT	ENSP00000429140.1:n.48+6940_48+6941delinsCT
ENST00000522368.5:c.373+262_373+263delinsCT
ENST00000522394.1:c.122+344_122+345delinsCT	ENSP00000429578.1:n.122+344_122+345delinsCT
ENST00000523957.1:c.*127+262_*127+263delinsCT	ENSP00000427830.1:n.*127+262_*127+263delinsCT
ENST00000621845.1:c.42+262_42+263delinsCT	ENSP00000484318.1:n.42+262_42+263delinsCT
NM_001172477.1:c.420+262_420+263delinsCT , LRG_788t1:c.420+262_420+263delinsCT	NP_001165948.1:n.420+262_420+263delinsCT
NM_001172478.1:c.49-5853_49-5852delinsCT	NP_001165949.1:n.49-5853_49-5852delinsCT
NM_015713.4:c.204+262_204+263delinsCT , LRG_788t2:c.204+262_204+263delinsCT	NP_056528.2:n.204+262_204+263delinsCT
NM_001172478.2:c.49-5853_49-5852delinsCT	NP_001165949.1:n.49-5853_49-5852delinsCT
NM_015713.5:c.204+262_204+263delinsCT MANE Select	NP_056528.2:n.204+262_204+263delinsCT