Canonical Allele Identifier: CA347547763

Gene: REEP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86232802C>G , CM000664.2:g.86232802C>G	GRCh38
NC_000002.11:g.86459925C>G , CM000664.1:g.86459925C>G	GRCh37
NC_000002.10:g.86313436C>G	NCBI36
NG_013037.1:g.110282G>C , LRG_713:g.110282G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001371279.1:c.418G>C MANE Select	NP_001358208.1:p.Gly140Arg
ENST00000538924.7:c.418G>C MANE Select	ENSP00000438346.3:p.Gly140Arg
NM_001164730.1:c.439G>C , LRG_713t1:c.439G>C	NP_001158202.1:p.Gly147Arg
NM_001164730.2:c.439G>C	NP_001158202.1:p.Gly147Arg
NM_001164731.1:c.337G>C	NP_001158203.1:p.Gly113Arg
NM_001164731.2:c.337G>C	NP_001158203.1:p.Gly113Arg
NM_001164732.1:c.183G>C	NP_001158204.1:p.Trp61Cys
NM_001164732.2:c.183G>C	NP_001158204.1:p.Trp61Cys
NM_001371280.1:c.418-15692G>C	NP_001358209.1:n.418-15692G>C
NM_022912.2:c.418G>C , LRG_713t2:c.418G>C	NP_075063.1:p.Gly140Arg
NM_022912.3:c.418G>C	NP_075063.1:p.Gly140Arg
ENST00000165698.9:c.418G>C	ENSP00000165698.5:p.Gly140Arg
ENST00000428491.5:c.337G>C	ENSP00000400607.1:p.Gly113Arg
ENST00000437769.5:c.183G>C	ENSP00000401140.1:p.Trp61Cys
ENST00000453231.5:c.439G>C	ENSP00000392197.1:p.Gly147Arg
ENST00000453231.6:c.439G>C	ENSP00000392197.2:p.Gly147Arg
ENST00000473407.5:n.508G>C
ENST00000490915.5:n.440G>C
ENST00000535845.5:c.337G>C	ENSP00000437567.1:p.Gly113Arg
ENST00000535845.6:c.337G>C	ENSP00000437567.1:p.Gly113Arg
ENST00000538924.5:c.439G>C	ENSP00000438346.1:p.Gly147Arg
ENST00000541910.5:c.183G>C	ENSP00000442681.1:p.Trp61Cys
ENST00000541910.6:c.183G>C	ENSP00000442681.1:p.Trp61Cys
ENST00000642243.1:c.526G>C	ENSP00000494960.1:p.Gly176Arg
ENST00000643817.1:c.376G>C	ENSP00000495610.1:p.Gly126Arg
ENST00000643817.2:c.418G>C	ENSP00000495610.2:p.Gly140Arg
ENST00000644644.1:c.427G>C	ENSP00000494305.1:p.Gly143Arg
ENST00000686220.1:c.337G>C	ENSP00000509904.1:p.Gly113Arg
ENST00000688400.1:c.106G>C	ENSP00000510490.1:p.Gly36Arg
ENST00000689156.1:c.418-15692G>C	ENSP00000509143.1:n.418-15692G>C
ENST00000691093.1:c.238G>C	ENSP00000509465.1:p.Gly80Arg
ENST00000691703.1:c.418G>C	ENSP00000508496.1:p.Gly140Arg
ENST00000692664.1:c.268G>C	ENSP00000508656.1:p.Gly90Arg
ENST00000693329.1:c.418G>C	ENSP00000508490.1:p.Gly140Arg
XM_005264502.1:c.418G>C	XP_005264559.1:p.Gly140Arg
XM_005264502.2:c.418G>C	XP_005264559.1:p.Gly140Arg
XM_005264504.1:c.304G>C	XP_005264561.1:p.Gly102Arg
XM_011533043.1:c.439G>C	XP_011531345.1:p.Gly147Arg
XM_011533044.1:c.400G>C	XP_011531346.1:p.Gly134Arg
XM_011533045.1:c.394G>C	XP_011531347.1:p.Gly132Arg
XM_011533045.2:c.394G>C	XP_011531347.1:p.Gly132Arg
XM_011533046.1:c.439G>C	XP_011531348.1:p.Gly147Arg
XM_017004725.1:c.439G>C	XP_016860214.1:p.Gly147Arg
XM_017004726.1:c.439G>C	XP_016860215.1:p.Gly147Arg
XM_017004727.1:c.439G>C	XP_016860216.1:p.Gly147Arg