Canonical Allele Identifier: CA19284480
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23692600C>T , CM000663.2:g.23692600C>T GRCh38
NC_000001.10:g.24019090C>T , CM000663.1:g.24019090C>T GRCh37
NC_000001.9:g.23891677C>T NCBI36
NG_011741.1:g.5797C>T
NG_011741.2:g.5822C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374550.8:c.7-12C>T ENSP00000363676.4:n.7-12C>T
ENST00000443624.6:n.25-9C>T
ENST00000458455.2:c.-36C>T ENSP00000398888.2:n.-36C>T
ENST00000467075.2:c.*103-9C>T ENSP00000493634.1:n.*103-9C>T
ENST00000643754.2:c.7-9C>T MANE Select ENSP00000496250.1:n.7-9C>T
ENST00000374550.7:c.7-9C>T ENSP00000363676.3:n.7-9C>T
ENST00000467075.1:n.227-9C>T
ENST00000482370.1:n.295C>T
NM_000975.3:c.7-9C>T NP_000966.2:n.7-9C>T
NM_001199802.1:c.7-12C>T NP_001186731.1:n.7-12C>T
NM_000975.5:c.7-9C>T MANE Select NP_000966.2:n.7-9C>T