Canonical Allele Identifier: CA583906539

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208227del , CM000670.2:g.102208227del	GRCh38
NC_000008.10:g.103220455del , CM000670.1:g.103220455del	GRCh37
NC_000008.9:g.103289631del	NCBI36
NG_016617.1:g.35892del , LRG_788:g.35892del

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.962del MANE Select	NP_056528.2:p.Thr321LysfsTer?
ENST00000251810.8:c.962del MANE Select	ENSP00000251810.3:p.Thr321LysfsTer?
NM_001172477.1:c.1178del , LRG_788t1:c.1178del	NP_001165948.1:p.Thr393LysfsTer?
NM_001172478.1:c.806del	NP_001165949.1:p.Thr269LysfsTer?
NM_001172478.2:c.806del	NP_001165949.1:p.Thr269LysfsTer?
NM_015713.4:c.962del , LRG_788t2:c.962del	NP_056528.2:p.Thr321LysfsTer?
ENST00000251810.7:c.962del	ENSP00000251810.3:p.Thr321LysfsTer?
ENST00000395910.6:n.349del
ENST00000395912.6:c.806del	ENSP00000379248.2:p.Thr269LysfsTer?
ENST00000519317.5:c.326del	ENSP00000430641.1:p.Thr109LysfsTer?
ENST00000519962.5:c.107del	ENSP00000429140.1:p.Thr36LysfsTer?
ENST00000522368.5:c.1131del
ENST00000522394.1:c.295del	ENSP00000429578.1:n.295del
ENST00000621845.1:c.800del	ENSP00000484318.1:p.Thr267LysfsTer?