Canonical Allele Identifier: CA338991366
Community Standard Title: NM_000975.5(RPL11):c.28A>T (p.Asn10Tyr)
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23692630A>T , CM000663.2:g.23692630A>T GRCh38
NC_000001.10:g.24019120A>T , CM000663.1:g.24019120A>T GRCh37
NC_000001.9:g.23891707A>T NCBI36
NG_011741.1:g.5827A>T
NG_011741.2:g.5852A>T

Transcript Alleles

HGVS Amino-acid Change
NM_000975.5:c.28A>T MANE Select NP_000966.2:p.Asn10Tyr
ENST00000643754.2:c.28A>T MANE Select ENSP00000496250.1:p.Asn10Tyr
NM_000975.3:c.28A>T NP_000966.2:p.Asn10Tyr
NM_001199802.1:c.25A>T NP_001186731.1:p.Asn9Tyr
ENST00000374550.7:c.28A>T ENSP00000363676.3:p.Asn10Tyr
ENST00000374550.8:c.25A>T ENSP00000363676.4:p.Asn9Tyr
ENST00000443624.5:c.22A>T ENSP00000390839.1:p.Asn8Tyr
ENST00000443624.6:n.46A>T
ENST00000458455.1:c.22A>T ENSP00000398888.1:p.Asn8Tyr
ENST00000458455.2:c.-6A>T ENSP00000398888.2:n.-6A>T
ENST00000467075.1:n.248A>T
ENST00000467075.2:c.*124A>T ENSP00000493634.1:n.*124A>T
ENST00000482370.1:n.325A>T
ENST00000482370.2:n.22A>T