Canonical Allele Identifier: CA521902935

Gene: RPL11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23692603T>G , CM000663.2:g.23692603T>G	GRCh38
NC_000001.10:g.24019093T>G , CM000663.1:g.24019093T>G	GRCh37
NC_000001.9:g.23891680T>G	NCBI36
NG_011741.1:g.5800T>G
NG_011741.2:g.5825T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000975.5:c.7-6T>G MANE Select	NP_000966.2:n.7-6T>G
ENST00000643754.2:c.7-6T>G MANE Select	ENSP00000496250.1:n.7-6T>G
NM_000975.3:c.7-6T>G	NP_000966.2:n.7-6T>G
NM_001199802.1:c.7-9T>G	NP_001186731.1:n.7-9T>G
ENST00000374550.7:c.7-6T>G	ENSP00000363676.3:n.7-6T>G
ENST00000374550.8:c.7-9T>G	ENSP00000363676.4:n.7-9T>G
ENST00000443624.6:n.25-6T>G
ENST00000458455.2:c.-33T>G	ENSP00000398888.2:n.-33T>G
ENST00000467075.1:n.227-6T>G
ENST00000467075.2:c.*103-6T>G	ENSP00000493634.1:n.*103-6T>G
ENST00000482370.1:n.298T>G