Canonical Allele Identifier: CA2781538874

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231882_102231883insG , CM000670.2:g.102231882_102231883insG	GRCh38
NC_000008.10:g.103244110_103244111insG , CM000670.1:g.103244110_103244111insG	GRCh37
NC_000008.9:g.103313286_103313287insG	NCBI36
NG_016617.1:g.12236_12237insC , LRG_788:g.12236_12237insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+266_204+267insC MANE Select	ENSP00000251810.3:n.204+266_204+267insC
ENST00000251810.7:c.204+266_204+267insC	ENSP00000251810.3:n.204+266_204+267insC
ENST00000395912.6:c.49-5849_49-5848insC	ENSP00000379248.2:n.49-5849_49-5848insC
ENST00000517517.1:n.513+266_513+267insC
ENST00000519317.5:c.48+6944_48+6945insC	ENSP00000430641.1:n.48+6944_48+6945insC
ENST00000519962.5:c.48+6944_48+6945insC	ENSP00000429140.1:n.48+6944_48+6945insC
ENST00000522368.5:c.373+266_373+267insC
ENST00000522394.1:c.122+348_122+349insC	ENSP00000429578.1:n.122+348_122+349insC
ENST00000523957.1:c.*127+266_*127+267insC	ENSP00000427830.1:n.*127+266_*127+267insC
ENST00000621845.1:c.42+266_42+267insC	ENSP00000484318.1:n.42+266_42+267insC
NM_001172477.1:c.420+266_420+267insC , LRG_788t1:c.420+266_420+267insC	NP_001165948.1:n.420+266_420+267insC
NM_001172478.1:c.49-5849_49-5848insC	NP_001165949.1:n.49-5849_49-5848insC
NM_015713.4:c.204+266_204+267insC , LRG_788t2:c.204+266_204+267insC	NP_056528.2:n.204+266_204+267insC
NM_001172478.2:c.49-5849_49-5848insC	NP_001165949.1:n.49-5849_49-5848insC
NM_015713.5:c.204+266_204+267insC MANE Select	NP_056528.2:n.204+266_204+267insC