Canonical Allele Identifier: CA1630848565

Gene: RRM1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4138227A= , CM000673.2:g.4138227A=	GRCh38
NC_000011.9:g.4159457A= , CM000673.1:g.4159457A=	GRCh37
NC_000011.8:g.4116033A=	NCBI36
NG_027992.2:g.48534A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001033.5:c.2223A= MANE Select	NP_001024.1:p.Thr741=
ENST00000300738.10:c.2223A= MANE Select	ENSP00000300738.5:p.Thr741=
NM_001033.3:c.2223A=	NP_001024.1:p.Thr741=
NM_001033.4:c.2223A=	NP_001024.1:p.Thr741=
NM_001318064.1:c.1932A=	NP_001304993.1:p.Thr644=
NM_001318065.1:c.1209A=	NP_001304994.1:p.Thr403=
NM_001330193.1:c.1557A=	NP_001317122.1:p.Thr519=
ENST00000300738.9:c.2223A=	ENSP00000300738.5:p.Thr741=
ENST00000532170.5:c.*2099A=	ENSP00000435656.1:n.*2099A=
ENST00000533349.5:c.*1931A=	ENSP00000434069.1:n.*1931A=
ENST00000533495.5:c.*1371A=	ENSP00000436377.1:n.*1371A=
ENST00000534285.5:c.1557A=	ENSP00000431464.1:p.Thr519=
XM_011520277.1:c.1932A=	XP_011518579.1:p.Thr644=
XM_011520278.1:c.1557A=	XP_011518580.1:p.Thr519=
XM_011520279.1:c.1209A=	XP_011518581.1:p.Thr403=