Canonical Allele Identifier: CA2659929514

Gene: REEP1

Linked Data

• gnomAD v4: 2-86216868-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86216872_86216873del , CM000664.2:g.86216872_86216873del	GRCh38
NC_000002.11:g.86443995_86443996del , CM000664.1:g.86443995_86443996del	GRCh37
NC_000002.10:g.86297506_86297507del	NCBI36
NG_013037.1:g.126214_126215del , LRG_713:g.126214_126215del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643817.2:c.*169_*170del	ENSP00000495610.2:n.*169_*170del
ENST00000686220.1:c.*284_*285del	ENSP00000509904.1:n.*284_*285del
ENST00000687696.1:n.366_367del
ENST00000687927.1:n.1302_1303del
ENST00000688400.1:c.524_525del	ENSP00000510490.1:n.524_525del
ENST00000689156.1:c.*169_*170del	ENSP00000509143.1:n.*169_*170del
ENST00000691093.1:c.*230_*231del	ENSP00000509465.1:n.*230_*231del
ENST00000691703.1:c.*230_*231del	ENSP00000508496.1:n.*230_*231del
ENST00000692664.1:c.*230_*231del	ENSP00000508656.1:n.*230_*231del
ENST00000693329.1:c.*310_*311del	ENSP00000508490.1:n.*310_*311del
ENST00000453231.6:c.*230_*231del	ENSP00000392197.2:n.*230_*231del
ENST00000535845.6:c.*230_*231del	ENSP00000437567.1:n.*230_*231del
ENST00000538924.7:c.*169_*170del MANE Select	ENSP00000438346.3:n.*169_*170del
ENST00000541910.6:c.*169_*170del	ENSP00000442681.1:n.*169_*170del
ENST00000642243.1:c.1132_1133del	ENSP00000494960.1:n.1132_1133del
ENST00000643817.1:c.946_947del	ENSP00000495610.1:n.946_947del
ENST00000644644.1:c.1033_1034del	ENSP00000494305.1:n.1033_1034del
ENST00000646181.1:n.709_710del
ENST00000165698.9:c.*230_*231del	ENSP00000165698.5:n.*230_*231del
ENST00000535845.5:c.*230_*231del	ENSP00000437567.1:n.*230_*231del
ENST00000538924.5:c.*230_*231del	ENSP00000438346.1:n.*230_*231del
ENST00000541910.5:c.*169_*170del	ENSP00000442681.1:n.*169_*170del
NM_001164730.1:c.*230_*231del , LRG_713t1:c.*230_*231del	NP_001158202.1:n.*230_*231del
NM_001164731.1:c.*230_*231del	NP_001158203.1:n.*230_*231del
NM_001164732.1:c.*169_*170del	NP_001158204.1:n.*169_*170del
NM_022912.2:c.*230_*231del , LRG_713t2:c.*230_*231del	NP_075063.1:n.*230_*231del
XM_005264502.1:c.*169_*170del	XP_005264559.1:n.*169_*170del
XM_005264504.1:c.*169_*170del	XP_005264561.1:n.*169_*170del
XM_011533043.1:c.*169_*170del	XP_011531345.1:n.*169_*170del
XM_011533044.1:c.*169_*170del	XP_011531346.1:n.*169_*170del
XM_011533045.1:c.*169_*170del	XP_011531347.1:n.*169_*170del
XM_005264502.2:c.*169_*170del	XP_005264559.1:n.*169_*170del
XM_011533045.2:c.*169_*170del	XP_011531347.1:n.*169_*170del
XM_017004725.1:c.*169_*170del	XP_016860214.1:n.*169_*170del
XM_017004726.1:c.*230_*231del	XP_016860215.1:n.*230_*231del
XM_017004727.1:c.*230_*231del	XP_016860216.1:n.*230_*231del
NM_001164730.2:c.*230_*231del	NP_001158202.1:n.*230_*231del
NM_001164731.2:c.*230_*231del	NP_001158203.1:n.*230_*231del
NM_001164732.2:c.*169_*170del	NP_001158204.1:n.*169_*170del
NM_001371279.1:c.*169_*170del MANE Select	NP_001358208.1:n.*169_*170del
NM_001371280.1:c.*169_*170del	NP_001358209.1:n.*169_*170del
NM_022912.3:c.*230_*231del	NP_075063.1:n.*230_*231del