Canonical Allele Identifier: CA2466670179

Gene: RPL10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154399798C>T , CM000685.2:g.154399798C>T	GRCh38
NC_000023.10:g.153628139C>T , CM000685.1:g.153628139C>T	GRCh37
NC_000023.9:g.153281333C>T	NCBI36
NG_012884.2:g.17291G>A
NG_012890.2:g.6570C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006013.5:c.191-5C>T MANE Select	NP_006004.3:n.191-5C>T
ENST00000369817.7:c.191-5C>T MANE Select	ENSP00000358832.2:n.191-5C>T
NM_001256577.2:c.191-5C>T	NP_001243506.2:n.191-5C>T
NM_001256580.2:c.83-5C>T	NP_001243509.2:n.83-5C>T
NM_001303624.1:c.191-5C>T	NP_001290553.1:n.191-5C>T
NM_001303624.2:c.191-5C>T	NP_001290553.1:n.191-5C>T
NM_001303625.1:c.191-5C>T	NP_001290554.1:n.191-5C>T
NM_001303626.1:c.191-5C>T	NP_001290555.1:n.191-5C>T
NM_006013.4:c.191-5C>T	NP_006004.3:n.191-5C>T
ENST00000344746.8:c.191-5C>T	ENSP00000341730.4:n.191-5C>T
ENST00000369817.6:c.191-5C>T	ENSP00000358832.2:n.191-5C>T
ENST00000406022.6:c.38-5C>T	ENSP00000385621.2:n.38-5C>T
ENST00000424325.6:c.191-5C>T	ENSP00000413436.2:n.191-5C>T
ENST00000436473.5:c.191-5C>T	ENSP00000388600.1:n.191-5C>T
ENST00000451365.1:c.140-5C>T	ENSP00000406125.1:n.140-5C>T
ENST00000458500.5:c.191-5C>T	ENSP00000395025.1:n.191-5C>T
ENST00000467168.5:n.214-5C>T
ENST00000482732.1:n.616C>T
ENST00000485196.5:n.422-5C>T
ENST00000489200.5:n.424-5C>T
ENST00000491035.5:n.334-5C>T
ENST00000492572.5:n.562-5C>T
ENST00000618723.4:c.83-5C>T	ENSP00000479103.1:n.83-5C>T