Canonical Allele Identifier: CA338993022

Gene: RPL11

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23693914G>A , CM000663.2:g.23693914G>A	GRCh38
NC_000001.10:g.24020404G>A , CM000663.1:g.24020404G>A	GRCh37
NC_000001.9:g.23892991G>A	NCBI36
NG_011741.1:g.7111G>A
NG_011741.2:g.7136G>A

Transcript Alleles

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