Canonical Allele Identifier: CA2504853802

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208220_102208221insT , CM000670.2:g.102208220_102208221insT	GRCh38
NC_000008.10:g.103220448_103220449insT , CM000670.1:g.103220448_103220449insT	GRCh37
NC_000008.9:g.103289624_103289625insT	NCBI36
NG_016617.1:g.35898_35899insA , LRG_788:g.35898_35899insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.968_969insA MANE Select	ENSP00000251810.3:p.Phe323LeufsTer3
ENST00000251810.7:c.968_969insA	ENSP00000251810.3:p.Phe323LeufsTer3
ENST00000395910.6:n.355_356insA
ENST00000395912.6:c.812_813insA	ENSP00000379248.2:p.Phe271LeufsTer3
ENST00000519317.5:c.332_333insA	ENSP00000430641.1:p.Phe111LeufsTer3
ENST00000519962.5:c.113_114insA	ENSP00000429140.1:p.Phe38LeufsTer3
ENST00000522368.5:c.1137_1138insA
ENST00000522394.1:c.301_302insA	ENSP00000429578.1:n.301_302insA
ENST00000621845.1:c.806_807insA	ENSP00000484318.1:p.Phe269LeufsTer3
NM_001172477.1:c.1184_1185insA , LRG_788t1:c.1184_1185insA	NP_001165948.1:p.Phe395LeufsTer3
NM_001172478.1:c.812_813insA	NP_001165949.1:p.Phe271LeufsTer3
NM_015713.4:c.968_969insA , LRG_788t2:c.968_969insA	NP_056528.2:p.Phe323LeufsTer3
NM_001172478.2:c.812_813insA	NP_001165949.1:p.Phe271LeufsTer3
NM_015713.5:c.968_969insA MANE Select	NP_056528.2:p.Phe323LeufsTer3