Canonical Allele Identifier: CA1806686226

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232242_102232244delinsCTT , CM000670.2:g.102232242_102232244delinsCTT	GRCh38
NC_000008.10:g.103244470_103244472delinsCTT , CM000670.1:g.103244470_103244472delinsCTT	GRCh37
NC_000008.9:g.103313646_103313648delinsCTT	NCBI36
NG_016617.1:g.11875_11877delinsAAG , LRG_788:g.11875_11877delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.109_111delinsAAG MANE Select	ENSP00000251810.3:p.Lys37=
ENST00000251810.7:c.109_111delinsAAG	ENSP00000251810.3:p.Lys37=
ENST00000395912.6:c.49-6210_49-6208delinsAAG	ENSP00000379248.2:n.49-6210_49-6208delinsAAG
ENST00000517517.1:n.418_420delinsAAG
ENST00000519317.5:c.48+6583_48+6585delinsAAG	ENSP00000430641.1:n.48+6583_48+6585delinsAAG
ENST00000519962.5:c.48+6583_48+6585delinsAAG	ENSP00000429140.1:n.48+6583_48+6585delinsAAG
ENST00000522368.5:c.278_280delinsAAG
ENST00000522394.1:c.109_111delinsAAG	ENSP00000429578.1:p.Lys37=
ENST00000523957.1:c.*32_*34delinsAAG	ENSP00000427830.1:n.*32_*34delinsAAG
ENST00000621845.1:c.-54_-52delinsAAG	ENSP00000484318.1:n.-54_-52delinsAAG
NM_001172477.1:c.325_327delinsAAG , LRG_788t1:c.325_327delinsAAG	NP_001165948.1:p.Lys109=
NM_001172478.1:c.49-6210_49-6208delinsAAG	NP_001165949.1:n.49-6210_49-6208delinsAAG
NM_015713.4:c.109_111delinsAAG , LRG_788t2:c.109_111delinsAAG	NP_056528.2:p.Lys37=
NM_001172478.2:c.49-6210_49-6208delinsAAG	NP_001165949.1:n.49-6210_49-6208delinsAAG
NM_015713.5:c.109_111delinsAAG MANE Select	NP_056528.2:p.Lys37=