Canonical Allele Identifier: CA684225
Community Standard Title: NM_000975.5(RPL11):c.264+9A>T
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23693922A>T , CM000663.2:g.23693922A>T GRCh38
NC_000001.10:g.24020412A>T , CM000663.1:g.24020412A>T GRCh37
NC_000001.9:g.23892999A>T NCBI36
NG_011741.1:g.7119A>T
NG_011741.2:g.7144A>T

Transcript Alleles

HGVS Amino-acid Change
NM_000975.5:c.264+9A>T MANE Select NP_000966.2:n.264+9A>T
ENST00000643754.2:c.264+9A>T MANE Select ENSP00000496250.1:n.264+9A>T
NM_000975.3:c.264+9A>T NP_000966.2:n.264+9A>T
NM_001199802.1:c.261+9A>T NP_001186731.1:n.261+9A>T
ENST00000374550.7:c.264+9A>T ENSP00000363676.3:n.264+9A>T
ENST00000374550.8:c.261+9A>T ENSP00000363676.4:n.261+9A>T
ENST00000443624.5:c.258+9A>T ENSP00000390839.1:n.258+9A>T
ENST00000443624.6:n.282+9A>T
ENST00000458455.1:c.258+9A>T ENSP00000398888.1:n.258+9A>T
ENST00000458455.2:c.231+9A>T ENSP00000398888.2:n.231+9A>T
ENST00000467075.2:c.*360+9A>T ENSP00000493634.1:n.*360+9A>T
ENST00000482370.1:n.561+9A>T
ENST00000482370.2:n.258+9A>T