Canonical Allele Identifier: CA1806674610

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102207996_102208001delinsTTAGAA , CM000670.2:g.102207996_102208001delinsTTAGAA	GRCh38
NC_000008.10:g.103220224_103220229delinsTTAGAA , CM000670.1:g.103220224_103220229delinsTTAGAA	GRCh37
NC_000008.9:g.103289400_103289405delinsTTAGAA	NCBI36
NG_016617.1:g.36118_36123delinsTTCTAA , LRG_788:g.36118_36123delinsTTCTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.*132_*137delinsTTCTAA MANE Select	ENSP00000251810.3:n.*132_*137delinsTTCTAA
ENST00000251810.7:c.*132_*137delinsTTCTAA	ENSP00000251810.3:n.*132_*137delinsTTCTAA
ENST00000395910.6:n.575_580delinsTTCTAA
ENST00000522368.5:c.1357_1362delinsTTCTAA
ENST00000621845.1:c.*132_*137delinsTTCTAA	ENSP00000484318.1:n.*132_*137delinsTTCTAA
NM_001172477.1:c.*132_*137delinsTTCTAA , LRG_788t1:c.*132_*137delinsTTCTAA	NP_001165948.1:n.*132_*137delinsTTCTAA
NM_001172478.1:c.*132_*137delinsTTCTAA	NP_001165949.1:n.*132_*137delinsTTCTAA
NM_015713.4:c.*132_*137delinsTTCTAA , LRG_788t2:c.*132_*137delinsTTCTAA	NP_056528.2:n.*132_*137delinsTTCTAA
NM_001172478.2:c.*132_*137delinsTTCTAA	NP_001165949.1:n.*132_*137delinsTTCTAA
NM_015713.5:c.*132_*137delinsTTCTAA MANE Select	NP_056528.2:n.*132_*137delinsTTCTAA