Canonical Allele Identifier: CA10561854

Gene: RPL10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154399848G>C , CM000685.2:g.154399848G>C	GRCh38
NC_000023.10:g.153628189G>C , CM000685.1:g.153628189G>C	GRCh37
NC_000023.9:g.153281383G>C	NCBI36
NG_012884.2:g.17241C>G
NG_012890.2:g.6620G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006013.5:c.236G>C MANE Select	NP_006004.3:p.Ser79Thr
ENST00000369817.7:c.236G>C MANE Select	ENSP00000358832.2:p.Ser79Thr
NM_001256577.2:c.236G>C	NP_001243506.2:p.Ser79Thr
NM_001256580.2:c.128G>C	NP_001243509.2:p.Ser43Thr
NM_001303624.1:c.236G>C	NP_001290553.1:p.Ser79Thr
NM_001303624.2:c.236G>C	NP_001290553.1:p.Ser79Thr
NM_001303625.1:c.236G>C	NP_001290554.1:p.Ser79Thr
NM_001303626.1:c.236G>C	NP_001290555.1:p.Ser79Thr
NM_006013.4:c.236G>C	NP_006004.3:p.Ser79Thr
ENST00000344746.8:c.236G>C	ENSP00000341730.4:p.Ser79Thr
ENST00000369817.6:c.236G>C	ENSP00000358832.2:p.Ser79Thr
ENST00000406022.6:c.83G>C	ENSP00000385621.2:p.Ser28Thr
ENST00000424325.6:c.236G>C	ENSP00000413436.2:p.Ser79Thr
ENST00000436473.5:c.236G>C	ENSP00000388600.1:p.Ser79Thr
ENST00000451365.1:c.185G>C	ENSP00000406125.1:p.Ser62Thr
ENST00000458500.5:c.236G>C	ENSP00000395025.1:p.Ser79Thr
ENST00000467168.5:n.259G>C
ENST00000482732.1:n.666G>C
ENST00000485196.5:n.467G>C
ENST00000489200.5:n.469G>C
ENST00000491035.5:n.379G>C
ENST00000492572.5:n.607G>C
ENST00000618723.4:c.128G>C	ENSP00000479103.1:p.Ser43Thr