Canonical Allele Identifier: CA1748764
Community Standard Title: NM_001371279.1(REEP1):c.371G>A (p.Arg124Gln)
Gene: REEP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.86252003C>T , CM000664.2:g.86252003C>T GRCh38
NC_000002.11:g.86479126C>T , CM000664.1:g.86479126C>T GRCh37
NC_000002.10:g.86332637C>T NCBI36
NG_013037.1:g.91081G>A , LRG_713:g.91081G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001371279.1:c.371G>A MANE Select NP_001358208.1:p.Arg124Gln
ENST00000538924.7:c.371G>A MANE Select ENSP00000438346.3:p.Arg124Gln
NM_001164730.1:c.392G>A , LRG_713t1:c.392G>A NP_001158202.1:p.Arg131Gln
NM_001164730.2:c.392G>A NP_001158202.1:p.Arg131Gln
NM_001164731.1:c.290G>A NP_001158203.1:p.Arg97Gln
NM_001164731.2:c.290G>A NP_001158203.1:p.Arg97Gln
NM_001164732.1:c.182+11962G>A NP_001158204.1:n.182+11962G>A
NM_001164732.2:c.182+11962G>A NP_001158204.1:n.182+11962G>A
NM_001371280.1:c.371G>A NP_001358209.1:p.Arg124Gln
NM_022912.2:c.371G>A , LRG_713t2:c.371G>A NP_075063.1:p.Arg124Gln
NM_022912.3:c.371G>A NP_075063.1:p.Arg124Gln
ENST00000165698.9:c.371G>A ENSP00000165698.5:p.Arg124Gln
ENST00000428491.5:c.290G>A ENSP00000400607.1:p.Arg97Gln
ENST00000437769.5:c.182+11962G>A ENSP00000401140.1:n.182+11962G>A
ENST00000453231.5:c.392G>A ENSP00000392197.1:p.Arg131Gln
ENST00000453231.6:c.392G>A ENSP00000392197.2:p.Arg131Gln
ENST00000473407.5:n.461G>A
ENST00000489855.2:c.307G>A
ENST00000490915.5:n.393G>A
ENST00000535845.5:c.290G>A ENSP00000437567.1:p.Arg97Gln
ENST00000535845.6:c.290G>A ENSP00000437567.1:p.Arg97Gln
ENST00000538924.5:c.392G>A ENSP00000438346.1:p.Arg131Gln
ENST00000541910.5:c.182+11962G>A ENSP00000442681.1:n.182+11962G>A
ENST00000541910.6:c.182+11962G>A ENSP00000442681.1:n.182+11962G>A
ENST00000642243.1:c.329G>A ENSP00000494960.1:p.Arg110Gln
ENST00000643817.1:c.329G>A ENSP00000495610.1:p.Arg110Gln
ENST00000643817.2:c.371G>A ENSP00000495610.2:p.Arg124Gln
ENST00000644644.1:c.329G>A ENSP00000494305.1:p.Arg110Gln
ENST00000686220.1:c.290G>A ENSP00000509904.1:p.Arg97Gln
ENST00000688400.1:c.106-19201G>A ENSP00000510490.1:n.106-19201G>A
ENST00000689156.1:c.371G>A ENSP00000509143.1:p.Arg124Gln
ENST00000691093.1:c.191G>A ENSP00000509465.1:p.Arg64Gln
ENST00000691703.1:c.371G>A ENSP00000508496.1:p.Arg124Gln
ENST00000692664.1:c.221G>A ENSP00000508656.1:p.Arg74Gln
ENST00000693329.1:c.371G>A ENSP00000508490.1:p.Arg124Gln
XM_005264502.1:c.371G>A XP_005264559.1:p.Arg124Gln
XM_005264502.2:c.371G>A XP_005264559.1:p.Arg124Gln
XM_005264504.1:c.257G>A XP_005264561.1:p.Arg86Gln
XM_011533043.1:c.392G>A XP_011531345.1:p.Arg131Gln
XM_011533044.1:c.353G>A XP_011531346.1:p.Arg118Gln
XM_011533045.1:c.347G>A XP_011531347.1:p.Arg116Gln
XM_011533045.2:c.347G>A XP_011531347.1:p.Arg116Gln
XM_011533046.1:c.392G>A XP_011531348.1:p.Arg131Gln
XM_017004725.1:c.392G>A XP_016860214.1:p.Arg131Gln
XM_017004726.1:c.392G>A XP_016860215.1:p.Arg131Gln
XM_017004727.1:c.392G>A XP_016860216.1:p.Arg131Gln