Canonical Allele Identifier: CA337297085

Gene: RPL10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154400774C>T , CM000685.2:g.154400774C>T	GRCh38
NC_000023.10:g.153629115C>T , CM000685.1:g.153629115C>T	GRCh37
NC_000023.9:g.153282309C>T	NCBI36
NG_012884.2:g.16315G>A
NG_012890.2:g.7546C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006013.5:c.565C>T MANE Select	NP_006004.3:p.Arg189Trp
ENST00000369817.7:c.565C>T MANE Select	ENSP00000358832.2:p.Arg189Trp
NM_001256577.2:c.402C>T	NP_001243506.2:p.Ser134=
NM_001256580.2:c.457C>T	NP_001243509.2:p.Arg153Trp
NM_001303624.1:c.565C>T	NP_001290553.1:p.Arg189Trp
NM_001303624.2:c.565C>T	NP_001290553.1:p.Arg189Trp
NM_001303625.1:c.565C>T	NP_001290554.1:p.Arg189Trp
NM_001303626.1:c.*116C>T	NP_001290555.1:n.*116C>T
NM_006013.4:c.565C>T	NP_006004.3:p.Arg189Trp
ENST00000344746.8:c.565C>T	ENSP00000341730.4:p.Arg189Trp
ENST00000369817.6:c.565C>T	ENSP00000358832.2:p.Arg189Trp
ENST00000406022.6:c.412C>T	ENSP00000385621.2:p.Arg138Trp
ENST00000424325.6:c.565C>T	ENSP00000413436.2:p.Arg189Trp
ENST00000427682.5:c.222+148C>T	ENSP00000405064.1:n.222+148C>T
ENST00000428169.1:c.222+148C>T	ENSP00000398047.1:n.222+148C>T
ENST00000436473.5:c.565C>T	ENSP00000388600.1:p.Arg189Trp
ENST00000449494.5:c.59+833C>T	ENSP00000407754.1:n.59+833C>T
ENST00000451365.1:c.278+833C>T	ENSP00000406125.1:n.278+833C>T
ENST00000458500.5:c.402C>T	ENSP00000395025.1:p.Ser134=
ENST00000467168.5:n.663C>T
ENST00000482732.1:n.1592C>T
ENST00000485196.5:n.796C>T
ENST00000489200.5:n.1395C>T
ENST00000491035.5:n.1230C>T
ENST00000492572.5:n.1533C>T
ENST00000618723.4:c.457C>T	ENSP00000479103.1:p.Arg153Trp