Canonical Allele Identifier: CA1948963843

Gene: RRM1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4138238C= , CM000673.2:g.4138238C=	GRCh38
NC_000011.9:g.4159468C= , CM000673.1:g.4159468C=	GRCh37
NC_000011.8:g.4116044C=	NCBI36
NG_027992.2:g.48545C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000300738.10:c.2234C= MANE Select	ENSP00000300738.5:p.Ala745=
ENST00000300738.9:c.2234C=	ENSP00000300738.5:p.Ala745=
ENST00000532170.5:c.*2110C=	ENSP00000435656.1:n.*2110C=
ENST00000533349.5:c.*1942C=	ENSP00000434069.1:n.*1942C=
ENST00000533495.5:c.*1382C=	ENSP00000436377.1:n.*1382C=
ENST00000534285.5:c.1568C=	ENSP00000431464.1:p.Ala523=
NM_001033.3:c.2234C=	NP_001024.1:p.Ala745=
XM_011520277.1:c.1943C=	XP_011518579.1:p.Ala648=
XM_011520278.1:c.1568C=	XP_011518580.1:p.Ala523=
XM_011520279.1:c.1220C=	XP_011518581.1:p.Ala407=
NM_001033.4:c.2234C=	NP_001024.1:p.Ala745=
NM_001318064.1:c.1943C=	NP_001304993.1:p.Ala648=
NM_001318065.1:c.1220C=	NP_001304994.1:p.Ala407=
NM_001330193.1:c.1568C=	NP_001317122.1:p.Ala523=
NM_001033.5:c.2234C= MANE Select	NP_001024.1:p.Ala745=