Canonical Allele Identifier: CA1141580662

Gene: RPL11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23693872C= , CM000663.2:g.23693872C=	GRCh38
NC_000001.10:g.24020362C= , CM000663.1:g.24020362C=	GRCh37
NC_000001.9:g.23892949C=	NCBI36
NG_011741.1:g.7069C=
NG_011741.2:g.7094C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000975.5:c.223C= MANE Select	NP_000966.2:p.Arg75=
ENST00000643754.2:c.223C= MANE Select	ENSP00000496250.1:p.Arg75=
NM_000975.3:c.223C=	NP_000966.2:p.Arg75=
NM_001199802.1:c.220C=	NP_001186731.1:p.Arg74=
ENST00000374550.7:c.223C=	ENSP00000363676.3:p.Arg75=
ENST00000374550.8:c.220C=	ENSP00000363676.4:p.Arg74=
ENST00000443624.5:c.217C=	ENSP00000390839.1:p.Arg73=
ENST00000443624.6:n.241C=
ENST00000458455.1:c.217C=	ENSP00000398888.1:p.Arg73=
ENST00000458455.2:c.190C=	ENSP00000398888.2:p.Arg64=
ENST00000467075.2:c.*319C=	ENSP00000493634.1:n.*319C=
ENST00000482370.1:n.520C=
ENST00000482370.2:n.217C=