Canonical Allele Identifier: CA338991949
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23692744C>T , CM000663.2:g.23692744C>T GRCh38
NC_000001.10:g.24019234C>T , CM000663.1:g.24019234C>T GRCh37
NC_000001.9:g.23891821C>T NCBI36
NG_011741.1:g.5941C>T
NG_011741.2:g.5966C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374550.8:c.139C>T ENSP00000363676.4:p.Pro47Ser
ENST00000443624.6:n.160C>T
ENST00000458455.2:c.109C>T ENSP00000398888.2:p.Pro37Ser
ENST00000467075.2:c.*238C>T ENSP00000493634.1:n.*238C>T
ENST00000482370.2:n.136C>T
ENST00000643754.2:c.142C>T MANE Select ENSP00000496250.1:p.Pro48Ser
ENST00000374550.7:c.142C>T ENSP00000363676.3:p.Pro48Ser
ENST00000443624.5:c.136C>T ENSP00000390839.1:p.Pro46Ser
ENST00000458455.1:c.136C>T ENSP00000398888.1:p.Pro46Ser
ENST00000467075.1:n.362C>T
ENST00000482370.1:n.439C>T
NM_000975.3:c.142C>T NP_000966.2:p.Pro48Ser
NM_001199802.1:c.139C>T NP_001186731.1:p.Pro47Ser
NM_000975.5:c.142C>T MANE Select NP_000966.2:p.Pro48Ser