Canonical Allele Identifier: CA2557779662

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231881_102231882insGAAA , CM000670.2:g.102231881_102231882insGAAA	GRCh38
NC_000008.10:g.103244109_103244110insGAAA , CM000670.1:g.103244109_103244110insGAAA	GRCh37
NC_000008.9:g.103313285_103313286insGAAA	NCBI36
NG_016617.1:g.12240_12241insCTTT , LRG_788:g.12240_12241insCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+270_204+271insCTTT MANE Select	ENSP00000251810.3:n.204+270_204+271insCTTT
ENST00000251810.7:c.204+270_204+271insCTTT	ENSP00000251810.3:n.204+270_204+271insCTTT
ENST00000395912.6:c.49-5845_49-5844insCTTT	ENSP00000379248.2:n.49-5845_49-5844insCTTT
ENST00000517517.1:n.513+270_513+271insCTTT
ENST00000519317.5:c.48+6948_48+6949insCTTT	ENSP00000430641.1:n.48+6948_48+6949insCTTT
ENST00000519962.5:c.48+6948_48+6949insCTTT	ENSP00000429140.1:n.48+6948_48+6949insCTTT
ENST00000522368.5:c.373+270_373+271insCTTT
ENST00000522394.1:c.122+352_122+353insCTTT	ENSP00000429578.1:n.122+352_122+353insCTTT
ENST00000523957.1:c.*127+270_*127+271insCTTT	ENSP00000427830.1:n.*127+270_*127+271insCTTT
ENST00000621845.1:c.42+270_42+271insCTTT	ENSP00000484318.1:n.42+270_42+271insCTTT
NM_001172477.1:c.420+270_420+271insCTTT , LRG_788t1:c.420+270_420+271insCTTT	NP_001165948.1:n.420+270_420+271insCTTT
NM_001172478.1:c.49-5845_49-5844insCTTT	NP_001165949.1:n.49-5845_49-5844insCTTT
NM_015713.4:c.204+270_204+271insCTTT , LRG_788t2:c.204+270_204+271insCTTT	NP_056528.2:n.204+270_204+271insCTTT
NM_001172478.2:c.49-5845_49-5844insCTTT	NP_001165949.1:n.49-5845_49-5844insCTTT
NM_015713.5:c.204+270_204+271insCTTT MANE Select	NP_056528.2:n.204+270_204+271insCTTT