Canonical Allele Identifier: CA1267127097
Gene: REEP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.86216955_86216968delinsTGCGGATTTCTATG , CM000664.2:g.86216955_86216968delinsTGCGGATTTCTATG GRCh38
NC_000002.11:g.86444078_86444091delinsTGCGGATTTCTATG , CM000664.1:g.86444078_86444091delinsTGCGGATTTCTATG GRCh37
NC_000002.10:g.86297589_86297602delinsTGCGGATTTCTATG NCBI36
NG_013037.1:g.126116_126129delinsCATAGAAATCCGCA , LRG_713:g.126116_126129delinsCATAGAAATCCGCA

Transcript Alleles

HGVS Amino-acid change
ENST00000643817.2:c.*71_*84delinsCATAGAAATCCGCA ENSP00000495610.2:n.*71_*84delinsCATAGAAA...
ENST00000686220.1:c.*186_*199delinsCATAGAAATCCGCA ENSP00000509904.1:n.*186_*199delinsCATAGA...
ENST00000687696.1:n.268_281delinsCATAGAAATCCGCA
ENST00000687927.1:n.1204_1217delinsCATAGAAATCCGCA
ENST00000688400.1:c.426_439delinsCATAGAAATCCGCA ENSP00000510490.1:n.426_439delinsCATAGAAA...
ENST00000689156.1:c.*71_*84delinsCATAGAAATCCGCA ENSP00000509143.1:n.*71_*84delinsCATAGAAA...
ENST00000691093.1:c.*132_*145delinsCATAGAAATCCGCA ENSP00000509465.1:n.*132_*145delinsCATAGA...
ENST00000691703.1:c.*132_*145delinsCATAGAAATCCGCA ENSP00000508496.1:n.*132_*145delinsCATAGA...
ENST00000692664.1:c.*132_*145delinsCATAGAAATCCGCA ENSP00000508656.1:n.*132_*145delinsCATAGA...
ENST00000693329.1:c.*212_*225delinsCATAGAAATCCGCA ENSP00000508490.1:n.*212_*225delinsCATAGA...
ENST00000453231.6:c.*132_*145delinsCATAGAAATCCGCA ENSP00000392197.2:n.*132_*145delinsCATAGA...
ENST00000535845.6:c.*132_*145delinsCATAGAAATCCGCA ENSP00000437567.1:n.*132_*145delinsCATAGA...
ENST00000538924.7:c.*71_*84delinsCATAGAAATCCGCA MANE Select ENSP00000438346.3:n.*71_*84delinsCATAGAAA...
ENST00000541910.6:c.*71_*84delinsCATAGAAATCCGCA ENSP00000442681.1:n.*71_*84delinsCATAGAAA...
ENST00000642243.1:c.1034_1047delinsCATAGAAATCCGCA ENSP00000494960.1:n.1034_1047delinsCATAGA...
ENST00000643817.1:c.848_861delinsCATAGAAATCCGCA ENSP00000495610.1:n.848_861delinsCATAGAAA...
ENST00000644644.1:c.935_948delinsCATAGAAATCCGCA ENSP00000494305.1:n.935_948delinsCATAGAAA...
ENST00000646181.1:n.611_624delinsCATAGAAATCCGCA
ENST00000165698.9:c.*132_*145delinsCATAGAAATCCGCA ENSP00000165698.5:n.*132_*145delinsCATAGA...
ENST00000535845.5:c.*132_*145delinsCATAGAAATCCGCA ENSP00000437567.1:n.*132_*145delinsCATAGA...
ENST00000538924.5:c.*132_*145delinsCATAGAAATCCGCA ENSP00000438346.1:n.*132_*145delinsCATAGA...
ENST00000541910.5:c.*71_*84delinsCATAGAAATCCGCA ENSP00000442681.1:n.*71_*84delinsCATAGAAA...
NM_001164730.1:c.*132_*145delinsCATAGAAATCCGCA , LRG_713t1:c.*132_*145delinsCATAGAAATCCGCA NP_001158202.1:n.*132_*145delinsCATAGAAAT...
NM_001164731.1:c.*132_*145delinsCATAGAAATCCGCA NP_001158203.1:n.*132_*145delinsCATAGAAAT...
NM_001164732.1:c.*71_*84delinsCATAGAAATCCGCA NP_001158204.1:n.*71_*84delinsCATAGAAATCC...
NM_022912.2:c.*132_*145delinsCATAGAAATCCGCA , LRG_713t2:c.*132_*145delinsCATAGAAATCCGCA NP_075063.1:n.*132_*145delinsCATAGAAATCCG...
XM_005264502.1:c.*71_*84delinsCATAGAAATCCGCA XP_005264559.1:n.*71_*84delinsCATAGAAATCC...
XM_005264504.1:c.*71_*84delinsCATAGAAATCCGCA XP_005264561.1:n.*71_*84delinsCATAGAAATCC...
XM_011533043.1:c.*71_*84delinsCATAGAAATCCGCA XP_011531345.1:n.*71_*84delinsCATAGAAATCC...
XM_011533044.1:c.*71_*84delinsCATAGAAATCCGCA XP_011531346.1:n.*71_*84delinsCATAGAAATCC...
XM_011533045.1:c.*71_*84delinsCATAGAAATCCGCA XP_011531347.1:n.*71_*84delinsCATAGAAATCC...
XM_005264502.2:c.*71_*84delinsCATAGAAATCCGCA XP_005264559.1:n.*71_*84delinsCATAGAAATCC...
XM_011533045.2:c.*71_*84delinsCATAGAAATCCGCA XP_011531347.1:n.*71_*84delinsCATAGAAATCC...
XM_017004725.1:c.*71_*84delinsCATAGAAATCCGCA XP_016860214.1:n.*71_*84delinsCATAGAAATCC...
XM_017004726.1:c.*132_*145delinsCATAGAAATCCGCA XP_016860215.1:n.*132_*145delinsCATAGAAAT...
XM_017004727.1:c.*132_*145delinsCATAGAAATCCGCA XP_016860216.1:n.*132_*145delinsCATAGAAAT...
NM_001164730.2:c.*132_*145delinsCATAGAAATCCGCA NP_001158202.1:n.*132_*145delinsCATAGAAAT...
NM_001164731.2:c.*132_*145delinsCATAGAAATCCGCA NP_001158203.1:n.*132_*145delinsCATAGAAAT...
NM_001164732.2:c.*71_*84delinsCATAGAAATCCGCA NP_001158204.1:n.*71_*84delinsCATAGAAATCC...
NM_001371279.1:c.*71_*84delinsCATAGAAATCCGCA MANE Select NP_001358208.1:n.*71_*84delinsCATAGAAATCC...
NM_001371280.1:c.*71_*84delinsCATAGAAATCCGCA NP_001358209.1:n.*71_*84delinsCATAGAAATCC...
NM_022912.3:c.*132_*145delinsCATAGAAATCCGCA NP_075063.1:n.*132_*145delinsCATAGAAATCCG...