Canonical Allele Identifier: CA1806678413

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218944_102218945delinsTC , CM000670.2:g.102218944_102218945delinsTC	GRCh38
NC_000008.10:g.103231172_103231173delinsTC , CM000670.1:g.103231172_103231173delinsTC	GRCh37
NC_000008.9:g.103300348_103300349delinsTC	NCBI36
NG_016617.1:g.25174_25175delinsGA , LRG_788:g.25174_25175delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.553_554delinsGA MANE Select	ENSP00000251810.3:p.Glu185=
ENST00000251810.7:c.553_554delinsGA	ENSP00000251810.3:p.Glu185=
ENST00000395912.6:c.397_398delinsGA	ENSP00000379248.2:p.Glu133=
ENST00000519125.1:n.71_72delinsGA
ENST00000519317.5:c.49-4787_49-4786delinsGA	ENSP00000430641.1:n.49-4787_49-4786delinsGA
ENST00000519962.5:c.49-10660_49-10659delinsGA	ENSP00000429140.1:n.49-10660_49-10659delinsGA
ENST00000522368.5:c.722_723delinsGA
ENST00000522394.1:c.123-6056_123-6055delinsGA	ENSP00000429578.1:n.123-6056_123-6055delinsGA
ENST00000621845.1:c.391_392delinsGA	ENSP00000484318.1:p.Glu131=
NM_001172477.1:c.769_770delinsGA , LRG_788t1:c.769_770delinsGA	NP_001165948.1:p.Glu257=
NM_001172478.1:c.397_398delinsGA	NP_001165949.1:p.Glu133=
NM_015713.4:c.553_554delinsGA , LRG_788t2:c.553_554delinsGA	NP_056528.2:p.Glu185=
NM_001172478.2:c.397_398delinsGA	NP_001165949.1:p.Glu133=
NM_015713.5:c.553_554delinsGA MANE Select	NP_056528.2:p.Glu185=