Canonical Allele Identifier: CA2565827477

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208227_102208239del , CM000670.2:g.102208227_102208239del	GRCh38
NC_000008.10:g.103220455_103220467del , CM000670.1:g.103220455_103220467del	GRCh37
NC_000008.9:g.103289631_103289643del	NCBI36
NG_016617.1:g.35880_35892del , LRG_788:g.35880_35892del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.950_962del MANE Select	ENSP00000251810.3:p.Leu317Ter
ENST00000251810.7:c.950_962del	ENSP00000251810.3:p.Leu317Ter
ENST00000395910.6:n.337_349del
ENST00000395912.6:c.794_806del	ENSP00000379248.2:p.Leu265Ter
ENST00000519317.5:c.314_326del	ENSP00000430641.1:p.Leu105Ter
ENST00000519962.5:c.95_107del	ENSP00000429140.1:p.Leu32Ter
ENST00000522368.5:c.1119_1131del
ENST00000522394.1:c.283_295del	ENSP00000429578.1:n.283_295del
ENST00000621845.1:c.788_800del	ENSP00000484318.1:p.Leu263Ter
NM_001172477.1:c.1166_1178del , LRG_788t1:c.1166_1178del	NP_001165948.1:p.Leu389Ter
NM_001172478.1:c.794_806del	NP_001165949.1:p.Leu265Ter
NM_015713.4:c.950_962del , LRG_788t2:c.950_962del	NP_056528.2:p.Leu317Ter
NM_001172478.2:c.794_806del	NP_001165949.1:p.Leu265Ter
NM_015713.5:c.950_962del MANE Select	NP_056528.2:p.Leu317Ter