Canonical Allele Identifier: CA247239

Gene: RPL10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154400848C>G , CM000685.2:g.154400848C>G	GRCh38
NC_000023.10:g.153629189C>G , CM000685.1:g.153629189C>G	GRCh37
NC_000023.9:g.153282383C>G	NCBI36
NG_012884.2:g.16241G>C
NG_012890.2:g.7620C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006013.5:c.639C>G MANE Select	NP_006004.3:p.His213Gln
ENST00000369817.7:c.639C>G MANE Select	ENSP00000358832.2:p.His213Gln
NM_001256577.2:c.476C>G	NP_001243506.2:p.Thr159Ser
NM_001256580.2:c.531C>G	NP_001243509.2:p.His177Gln
NM_001303624.1:c.639C>G	NP_001290553.1:p.His213Gln
NM_001303624.2:c.639C>G	NP_001290553.1:p.His213Gln
NM_001303625.1:c.639C>G	NP_001290554.1:p.His213Gln
NM_001303626.1:c.*190C>G	NP_001290555.1:n.*190C>G
NM_006013.4:c.639C>G	NP_006004.3:p.His213Gln
ENST00000344746.8:c.639C>G	ENSP00000341730.4:p.His213Gln
ENST00000369817.6:c.639C>G	ENSP00000358832.2:p.His213Gln
ENST00000406022.6:c.486C>G	ENSP00000385621.2:p.His162Gln
ENST00000424325.6:c.639C>G	ENSP00000413436.2:p.His213Gln
ENST00000427682.5:c.222+222C>G	ENSP00000405064.1:n.222+222C>G
ENST00000428169.1:c.222+222C>G	ENSP00000398047.1:n.222+222C>G
ENST00000449494.5:c.59+907C>G	ENSP00000407754.1:n.59+907C>G
ENST00000451365.1:c.278+907C>G	ENSP00000406125.1:n.278+907C>G
ENST00000458500.5:c.476C>G	ENSP00000395025.1:p.Thr159Ser
ENST00000467168.5:n.737C>G
ENST00000482732.1:n.1666C>G
ENST00000489200.5:n.1469C>G
ENST00000491035.5:n.1304C>G
ENST00000492572.5:n.1607C>G
ENST00000618723.4:c.531C>G	ENSP00000479103.1:p.His177Gln