Canonical Allele Identifier: CA1806681644

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224875_102224878delinsCCAA , CM000670.2:g.102224875_102224878delinsCCAA	GRCh38
NC_000008.10:g.103237103_103237106delinsCCAA , CM000670.1:g.103237103_103237106delinsCCAA	GRCh37
NC_000008.9:g.103306279_103306282delinsCCAA	NCBI36
NG_016617.1:g.19241_19244delinsTTGG , LRG_788:g.19241_19244delinsTTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.455+7_455+10delinsTTGG MANE Select	ENSP00000251810.3:n.455+7_455+10delinsTTG...
ENST00000251810.7:c.455+7_455+10delinsTTGG	ENSP00000251810.3:n.455+7_455+10delinsTTG...
ENST00000395912.6:c.299+7_299+10delinsTTGG	ENSP00000379248.2:n.299+7_299+10delinsTTG...
ENST00000519317.5:c.49-10720_49-10717delinsTTGG	ENSP00000430641.1:n.49-10720_49-10717deli...
ENST00000519962.5:c.48+13949_48+13952delinsTTGG	ENSP00000429140.1:n.48+13949_48+13952deli...
ENST00000522368.5:c.624+7_624+10delinsTTGG
ENST00000522394.1:c.122+7353_122+7356delinsTTGG	ENSP00000429578.1:n.122+7353_122+7356deli...
ENST00000621845.1:c.293+7_293+10delinsTTGG	ENSP00000484318.1:n.293+7_293+10delinsTTG...
NM_001172477.1:c.671+7_671+10delinsTTGG , LRG_788t1:c.671+7_671+10delinsTTGG	NP_001165948.1:n.671+7_671+10delinsTTGG
NM_001172478.1:c.299+7_299+10delinsTTGG	NP_001165949.1:n.299+7_299+10delinsTTGG
NM_015713.4:c.455+7_455+10delinsTTGG , LRG_788t2:c.455+7_455+10delinsTTGG	NP_056528.2:n.455+7_455+10delinsTTGG
NM_001172478.2:c.299+7_299+10delinsTTGG	NP_001165949.1:n.299+7_299+10delinsTTGG
NM_015713.5:c.455+7_455+10delinsTTGG MANE Select	NP_056528.2:n.455+7_455+10delinsTTGG