Canonical Allele Identifier: CA10561914

Gene: RPL10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154400744G>A , CM000685.2:g.154400744G>A	GRCh38
NC_000023.10:g.153629085G>A , CM000685.1:g.153629085G>A	GRCh37
NC_000023.9:g.153282279G>A	NCBI36
NG_012884.2:g.16345C>T
NG_012890.2:g.7516G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006013.5:c.535G>A MANE Select	NP_006004.3:p.Asp179Asn
ENST00000369817.7:c.535G>A MANE Select	ENSP00000358832.2:p.Asp179Asn
NM_001256577.2:c.372G>A	NP_001243506.2:p.Leu124=
NM_001256580.2:c.427G>A	NP_001243509.2:p.Asp143Asn
NM_001303624.1:c.535G>A	NP_001290553.1:p.Asp179Asn
NM_001303624.2:c.535G>A	NP_001290553.1:p.Asp179Asn
NM_001303625.1:c.535G>A	NP_001290554.1:p.Asp179Asn
NM_001303626.1:c.*86G>A	NP_001290555.1:n.*86G>A
NM_006013.4:c.535G>A	NP_006004.3:p.Asp179Asn
ENST00000344746.8:c.535G>A	ENSP00000341730.4:p.Asp179Asn
ENST00000369817.6:c.535G>A	ENSP00000358832.2:p.Asp179Asn
ENST00000406022.6:c.382G>A	ENSP00000385621.2:p.Asp128Asn
ENST00000424325.6:c.535G>A	ENSP00000413436.2:p.Asp179Asn
ENST00000427682.5:c.222+118G>A	ENSP00000405064.1:n.222+118G>A
ENST00000428169.1:c.222+118G>A	ENSP00000398047.1:n.222+118G>A
ENST00000436473.5:c.535G>A	ENSP00000388600.1:p.Asp179Asn
ENST00000449494.5:c.59+803G>A	ENSP00000407754.1:n.59+803G>A
ENST00000451365.1:c.278+803G>A	ENSP00000406125.1:n.278+803G>A
ENST00000458500.5:c.372G>A	ENSP00000395025.1:p.Leu124=
ENST00000467168.5:n.633G>A
ENST00000482732.1:n.1562G>A
ENST00000485196.5:n.766G>A
ENST00000489200.5:n.1365G>A
ENST00000491035.5:n.1200G>A
ENST00000492572.5:n.1503G>A
ENST00000618723.4:c.427G>A	ENSP00000479103.1:p.Asp143Asn