Canonical Allele Identifier: CA2659929489

Gene: REEP1

Linked Data

• gnomAD v4: 2-86216848-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86216852del , CM000664.2:g.86216852del	GRCh38
NC_000002.11:g.86443975del , CM000664.1:g.86443975del	GRCh37
NC_000002.10:g.86297486del	NCBI36
NG_013037.1:g.126235del , LRG_713:g.126235del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643817.2:c.*190del	ENSP00000495610.2:n.*190del
ENST00000686220.1:c.*305del	ENSP00000509904.1:n.*305del
ENST00000687696.1:n.387del
ENST00000687927.1:n.1323del
ENST00000688400.1:c.545del	ENSP00000510490.1:n.545del
ENST00000689156.1:c.*190del	ENSP00000509143.1:n.*190del
ENST00000691093.1:c.*251del	ENSP00000509465.1:n.*251del
ENST00000691703.1:c.*251del	ENSP00000508496.1:n.*251del
ENST00000692664.1:c.*251del	ENSP00000508656.1:n.*251del
ENST00000693329.1:c.*331del	ENSP00000508490.1:n.*331del
ENST00000453231.6:c.*251del	ENSP00000392197.2:n.*251del
ENST00000535845.6:c.*251del	ENSP00000437567.1:n.*251del
ENST00000538924.7:c.*190del MANE Select	ENSP00000438346.3:n.*190del
ENST00000541910.6:c.*190del	ENSP00000442681.1:n.*190del
ENST00000642243.1:c.1153del	ENSP00000494960.1:n.1153del
ENST00000643817.1:c.967del	ENSP00000495610.1:n.967del
ENST00000644644.1:c.1054del	ENSP00000494305.1:n.1054del
ENST00000646181.1:n.730del
ENST00000165698.9:c.*251del	ENSP00000165698.5:n.*251del
ENST00000535845.5:c.*251del	ENSP00000437567.1:n.*251del
ENST00000538924.5:c.*251del	ENSP00000438346.1:n.*251del
ENST00000541910.5:c.*190del	ENSP00000442681.1:n.*190del
NM_001164730.1:c.*251del , LRG_713t1:c.*251del	NP_001158202.1:n.*251del
NM_001164731.1:c.*251del	NP_001158203.1:n.*251del
NM_001164732.1:c.*190del	NP_001158204.1:n.*190del
NM_022912.2:c.*251del , LRG_713t2:c.*251del	NP_075063.1:n.*251del
XM_005264502.1:c.*190del	XP_005264559.1:n.*190del
XM_005264504.1:c.*190del	XP_005264561.1:n.*190del
XM_011533043.1:c.*190del	XP_011531345.1:n.*190del
XM_011533044.1:c.*190del	XP_011531346.1:n.*190del
XM_011533045.1:c.*190del	XP_011531347.1:n.*190del
XM_005264502.2:c.*190del	XP_005264559.1:n.*190del
XM_011533045.2:c.*190del	XP_011531347.1:n.*190del
XM_017004725.1:c.*190del	XP_016860214.1:n.*190del
XM_017004726.1:c.*251del	XP_016860215.1:n.*251del
XM_017004727.1:c.*251del	XP_016860216.1:n.*251del
NM_001164730.2:c.*251del	NP_001158202.1:n.*251del
NM_001164731.2:c.*251del	NP_001158203.1:n.*251del
NM_001164732.2:c.*190del	NP_001158204.1:n.*190del
NM_001371279.1:c.*190del MANE Select	NP_001358208.1:n.*190del
NM_001371280.1:c.*190del	NP_001358209.1:n.*190del
NM_022912.3:c.*251del	NP_075063.1:n.*251del