Canonical Allele Identifier: CA415262226

Gene: RPL10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154400847A>T , CM000685.2:g.154400847A>T	GRCh38
NC_000023.10:g.153629188A>T , CM000685.1:g.153629188A>T	GRCh37
NC_000023.9:g.153282382A>T	NCBI36
NG_012884.2:g.16242T>A
NG_012890.2:g.7619A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006013.5:c.638A>T MANE Select	NP_006004.3:p.His213Leu
ENST00000369817.7:c.638A>T MANE Select	ENSP00000358832.2:p.His213Leu
NM_001256577.2:c.475A>T	NP_001243506.2:p.Thr159Ser
NM_001256580.2:c.530A>T	NP_001243509.2:p.His177Leu
NM_001303624.1:c.638A>T	NP_001290553.1:p.His213Leu
NM_001303624.2:c.638A>T	NP_001290553.1:p.His213Leu
NM_001303625.1:c.638A>T	NP_001290554.1:p.His213Leu
NM_001303626.1:c.*189A>T	NP_001290555.1:n.*189A>T
NM_006013.4:c.638A>T	NP_006004.3:p.His213Leu
ENST00000344746.8:c.638A>T	ENSP00000341730.4:p.His213Leu
ENST00000369817.6:c.638A>T	ENSP00000358832.2:p.His213Leu
ENST00000406022.6:c.485A>T	ENSP00000385621.2:p.His162Leu
ENST00000424325.6:c.638A>T	ENSP00000413436.2:p.His213Leu
ENST00000427682.5:c.222+221A>T	ENSP00000405064.1:n.222+221A>T
ENST00000428169.1:c.222+221A>T	ENSP00000398047.1:n.222+221A>T
ENST00000449494.5:c.59+906A>T	ENSP00000407754.1:n.59+906A>T
ENST00000451365.1:c.278+906A>T	ENSP00000406125.1:n.278+906A>T
ENST00000458500.5:c.475A>T	ENSP00000395025.1:p.Thr159Ser
ENST00000467168.5:n.736A>T
ENST00000482732.1:n.1665A>T
ENST00000489200.5:n.1468A>T
ENST00000491035.5:n.1303A>T
ENST00000492572.5:n.1606A>T
ENST00000618723.4:c.530A>T	ENSP00000479103.1:p.His177Leu