Canonical Allele Identifier: CA684167

Gene: RPL11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23692704G>C , CM000663.2:g.23692704G>C	GRCh38
NC_000001.10:g.24019194G>C , CM000663.1:g.24019194G>C	GRCh37
NC_000001.9:g.23891781G>C	NCBI36
NG_011741.1:g.5901G>C
NG_011741.2:g.5926G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000975.5:c.102G>C MANE Select	NP_000966.2:p.Thr34=
ENST00000643754.2:c.102G>C MANE Select	ENSP00000496250.1:p.Thr34=
NM_000975.3:c.102G>C	NP_000966.2:p.Thr34=
NM_001199802.1:c.99G>C	NP_001186731.1:p.Thr33=
ENST00000374550.7:c.102G>C	ENSP00000363676.3:p.Thr34=
ENST00000374550.8:c.99G>C	ENSP00000363676.4:p.Thr33=
ENST00000443624.5:c.96G>C	ENSP00000390839.1:p.Thr32=
ENST00000443624.6:n.120G>C
ENST00000458455.1:c.96G>C	ENSP00000398888.1:p.Thr32=
ENST00000458455.2:c.69G>C	ENSP00000398888.2:p.Thr23=
ENST00000467075.1:n.322G>C
ENST00000467075.2:c.*198G>C	ENSP00000493634.1:n.*198G>C
ENST00000482370.1:n.399G>C
ENST00000482370.2:n.96G>C