Canonical Allele Identifier: CA338992575
Community Standard Title: NM_000975.5(RPL11):c.158-1G>C
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23693806G>C , CM000663.2:g.23693806G>C GRCh38
NC_000001.10:g.24020296G>C , CM000663.1:g.24020296G>C GRCh37
NC_000001.9:g.23892883G>C NCBI36
NG_011741.1:g.7003G>C
NG_011741.2:g.7028G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000975.5:c.158-1G>C MANE Select NP_000966.2:n.158-1G>C
ENST00000643754.2:c.158-1G>C MANE Select ENSP00000496250.1:n.158-1G>C
NM_000975.3:c.158-1G>C NP_000966.2:n.158-1G>C
NM_001199802.1:c.155-1G>C NP_001186731.1:n.155-1G>C
ENST00000374550.7:c.158-1G>C ENSP00000363676.3:n.158-1G>C
ENST00000374550.8:c.155-1G>C ENSP00000363676.4:n.155-1G>C
ENST00000443624.5:c.152-1G>C ENSP00000390839.1:n.152-1G>C
ENST00000443624.6:n.176-1G>C
ENST00000458455.1:c.152-1G>C ENSP00000398888.1:n.152-1G>C
ENST00000458455.2:c.125-1G>C ENSP00000398888.2:n.125-1G>C
ENST00000467075.2:c.*254-1G>C ENSP00000493634.1:n.*254-1G>C
ENST00000482370.1:n.455-1G>C
ENST00000482370.2:n.152-1G>C