Canonical Allele Identifier: CA684156
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23692635C>T , CM000663.2:g.23692635C>T GRCh38
NC_000001.10:g.24019125C>T , CM000663.1:g.24019125C>T GRCh37
NC_000001.9:g.23891712C>T NCBI36
NG_011741.1:g.5832C>T
NG_011741.2:g.5857C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374550.8:c.30C>T ENSP00000363676.4:p.Pro10=
ENST00000443624.6:n.51C>T
ENST00000458455.2:c.-1C>T ENSP00000398888.2:n.-1C>T
ENST00000467075.2:c.*129C>T ENSP00000493634.1:n.*129C>T
ENST00000482370.2:n.27C>T
ENST00000643754.2:c.33C>T MANE Select ENSP00000496250.1:p.Pro11=
ENST00000374550.7:c.33C>T ENSP00000363676.3:p.Pro11=
ENST00000443624.5:c.27C>T ENSP00000390839.1:p.Pro9=
ENST00000458455.1:c.27C>T ENSP00000398888.1:p.Pro9=
ENST00000467075.1:n.253C>T
ENST00000482370.1:n.330C>T
NM_000975.3:c.33C>T NP_000966.2:p.Pro11=
NM_001199802.1:c.30C>T NP_001186731.1:p.Pro10=
NM_000975.5:c.33C>T MANE Select NP_000966.2:p.Pro11=