Canonical Allele Identifier: CA1806686074

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231901_102231902delinsAT , CM000670.2:g.102231901_102231902delinsAT	GRCh38
NC_000008.10:g.103244129_103244130delinsAT , CM000670.1:g.103244129_103244130delinsAT	GRCh37
NC_000008.9:g.103313305_103313306delinsAT	NCBI36
NG_016617.1:g.12217_12218delinsAT , LRG_788:g.12217_12218delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+247_204+248delinsAT MANE Select	ENSP00000251810.3:n.204+247_204+248delinsAT
ENST00000251810.7:c.204+247_204+248delinsAT	ENSP00000251810.3:n.204+247_204+248delinsAT
ENST00000395912.6:c.49-5868_49-5867delinsAT	ENSP00000379248.2:n.49-5868_49-5867delinsAT
ENST00000517517.1:n.513+247_513+248delinsAT
ENST00000519317.5:c.48+6925_48+6926delinsAT	ENSP00000430641.1:n.48+6925_48+6926delinsAT
ENST00000519962.5:c.48+6925_48+6926delinsAT	ENSP00000429140.1:n.48+6925_48+6926delinsAT
ENST00000522368.5:c.373+247_373+248delinsAT
ENST00000522394.1:c.122+329_122+330delinsAT	ENSP00000429578.1:n.122+329_122+330delinsAT
ENST00000523957.1:c.*127+247_*127+248delinsAT	ENSP00000427830.1:n.*127+247_*127+248delinsAT
ENST00000621845.1:c.42+247_42+248delinsAT	ENSP00000484318.1:n.42+247_42+248delinsAT
NM_001172477.1:c.420+247_420+248delinsAT , LRG_788t1:c.420+247_420+248delinsAT	NP_001165948.1:n.420+247_420+248delinsAT
NM_001172478.1:c.49-5868_49-5867delinsAT	NP_001165949.1:n.49-5868_49-5867delinsAT
NM_015713.4:c.204+247_204+248delinsAT , LRG_788t2:c.204+247_204+248delinsAT	NP_056528.2:n.204+247_204+248delinsAT
NM_001172478.2:c.49-5868_49-5867delinsAT	NP_001165949.1:n.49-5868_49-5867delinsAT
NM_015713.5:c.204+247_204+248delinsAT MANE Select	NP_056528.2:n.204+247_204+248delinsAT