Canonical Allele Identifier: CA1806686117

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232001_102232004delinsACAT , CM000670.2:g.102232001_102232004delinsACAT	GRCh38
NC_000008.10:g.103244229_103244232delinsACAT , CM000670.1:g.103244229_103244232delinsACAT	GRCh37
NC_000008.9:g.103313405_103313408delinsACAT	NCBI36
NG_016617.1:g.12115_12118delinsATGT , LRG_788:g.12115_12118delinsATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+145_204+148delinsATGT MANE Select	ENSP00000251810.3:n.204+145_204+148delinsATGT
ENST00000251810.7:c.204+145_204+148delinsATGT	ENSP00000251810.3:n.204+145_204+148delinsATGT
ENST00000395912.6:c.49-5970_49-5967delinsATGT	ENSP00000379248.2:n.49-5970_49-5967delinsATGT
ENST00000517517.1:n.513+145_513+148delinsATGT
ENST00000519317.5:c.48+6823_48+6826delinsATGT	ENSP00000430641.1:n.48+6823_48+6826delinsATGT
ENST00000519962.5:c.48+6823_48+6826delinsATGT	ENSP00000429140.1:n.48+6823_48+6826delinsATGT
ENST00000522368.5:c.373+145_373+148delinsATGT
ENST00000522394.1:c.122+227_122+230delinsATGT	ENSP00000429578.1:n.122+227_122+230delinsATGT
ENST00000523957.1:c.*127+145_*127+148delinsATGT	ENSP00000427830.1:n.*127+145_*127+148delinsATGT
ENST00000621845.1:c.42+145_42+148delinsATGT	ENSP00000484318.1:n.42+145_42+148delinsATGT
NM_001172477.1:c.420+145_420+148delinsATGT , LRG_788t1:c.420+145_420+148delinsATGT	NP_001165948.1:n.420+145_420+148delinsATGT
NM_001172478.1:c.49-5970_49-5967delinsATGT	NP_001165949.1:n.49-5970_49-5967delinsATGT
NM_015713.4:c.204+145_204+148delinsATGT , LRG_788t2:c.204+145_204+148delinsATGT	NP_056528.2:n.204+145_204+148delinsATGT
NM_001172478.2:c.49-5970_49-5967delinsATGT	NP_001165949.1:n.49-5970_49-5967delinsATGT
NM_015713.5:c.204+145_204+148delinsATGT MANE Select	NP_056528.2:n.204+145_204+148delinsATGT