Canonical Allele Identifier: CA1806686028

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231848_102231850delinsGAC , CM000670.2:g.102231848_102231850delinsGAC	GRCh38
NC_000008.10:g.103244076_103244078delinsGAC , CM000670.1:g.103244076_103244078delinsGAC	GRCh37
NC_000008.9:g.103313252_103313254delinsGAC	NCBI36
NG_016617.1:g.12269_12271delinsGTC , LRG_788:g.12269_12271delinsGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+299_204+301delinsGTC MANE Select	ENSP00000251810.3:n.204+299_204+301delinsGTC
ENST00000251810.7:c.204+299_204+301delinsGTC	ENSP00000251810.3:n.204+299_204+301delinsGTC
ENST00000395912.6:c.49-5816_49-5814delinsGTC	ENSP00000379248.2:n.49-5816_49-5814delinsGTC
ENST00000517517.1:n.513+299_513+301delinsGTC
ENST00000519317.5:c.48+6977_48+6979delinsGTC	ENSP00000430641.1:n.48+6977_48+6979delinsGTC
ENST00000519962.5:c.48+6977_48+6979delinsGTC	ENSP00000429140.1:n.48+6977_48+6979delinsGTC
ENST00000522368.5:c.373+299_373+301delinsGTC
ENST00000522394.1:c.122+381_122+383delinsGTC	ENSP00000429578.1:n.122+381_122+383delinsGTC
ENST00000523957.1:c.*127+299_*127+301delinsGTC	ENSP00000427830.1:n.*127+299_*127+301delinsGTC
ENST00000621845.1:c.42+299_42+301delinsGTC	ENSP00000484318.1:n.42+299_42+301delinsGTC
NM_001172477.1:c.420+299_420+301delinsGTC , LRG_788t1:c.420+299_420+301delinsGTC	NP_001165948.1:n.420+299_420+301delinsGTC
NM_001172478.1:c.49-5816_49-5814delinsGTC	NP_001165949.1:n.49-5816_49-5814delinsGTC
NM_015713.4:c.204+299_204+301delinsGTC , LRG_788t2:c.204+299_204+301delinsGTC	NP_056528.2:n.204+299_204+301delinsGTC
NM_001172478.2:c.49-5816_49-5814delinsGTC	NP_001165949.1:n.49-5816_49-5814delinsGTC
NM_015713.5:c.204+299_204+301delinsGTC MANE Select	NP_056528.2:n.204+299_204+301delinsGTC