Canonical Allele Identifier: CA347544188

Gene: REEP1

Linked Data

• MyVariant Identifiers: chr2:g.86444187G>C (hg19) ; chr2:g.86217064G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86217064G>C , CM000664.2:g.86217064G>C	GRCh38
NC_000002.11:g.86444187G>C , CM000664.1:g.86444187G>C	GRCh37
NC_000002.10:g.86297698G>C	NCBI36
NG_013037.1:g.126020C>G , LRG_713:g.126020C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000643817.2:c.794C>G	ENSP00000495610.2:p.Ser265Ter
ENST00000686220.1:c.*90C>G	ENSP00000509904.1:n.*90C>G
ENST00000687696.1:n.172C>G
ENST00000687927.1:n.1108C>G
ENST00000688400.1:c.330C>G	ENSP00000510490.1:n.330C>G
ENST00000689156.1:c.464C>G	ENSP00000509143.1:p.Ser155Ter
ENST00000691093.1:c.*36C>G	ENSP00000509465.1:n.*36C>G
ENST00000691703.1:c.*36C>G	ENSP00000508496.1:n.*36C>G
ENST00000692664.1:c.*36C>G	ENSP00000508656.1:n.*36C>G
ENST00000693329.1:c.*116C>G	ENSP00000508490.1:n.*116C>G
ENST00000453231.6:c.*36C>G	ENSP00000392197.2:n.*36C>G
ENST00000535845.6:c.*36C>G	ENSP00000437567.1:n.*36C>G
ENST00000538924.7:c.830C>G MANE Select	ENSP00000438346.3:p.Ser277Ter
ENST00000541910.6:c.407C>G	ENSP00000442681.1:p.Ser136Ter
ENST00000642243.1:c.938C>G	ENSP00000494960.1:p.Ser313Ter
ENST00000643817.1:c.752C>G	ENSP00000495610.1:p.Ser251Ter
ENST00000644644.1:c.839C>G	ENSP00000494305.1:p.Ser280Ter
ENST00000646181.1:n.515C>G
ENST00000165698.9:c.*36C>G	ENSP00000165698.5:n.*36C>G
ENST00000535845.5:c.*36C>G	ENSP00000437567.1:n.*36C>G
ENST00000538924.5:c.*36C>G	ENSP00000438346.1:n.*36C>G
ENST00000541910.5:c.407C>G	ENSP00000442681.1:p.Ser136Ter
NM_001164730.1:c.*36C>G , LRG_713t1:c.*36C>G	NP_001158202.1:n.*36C>G
NM_001164731.1:c.*36C>G	NP_001158203.1:n.*36C>G
NM_001164732.1:c.407C>G	NP_001158204.1:p.Ser136Ter
NM_022912.2:c.*36C>G , LRG_713t2:c.*36C>G	NP_075063.1:n.*36C>G
XM_005264502.1:c.830C>G	XP_005264559.1:p.Ser277Ter
XM_005264504.1:c.716C>G	XP_005264561.1:p.Ser239Ter
XM_011533043.1:c.815C>G	XP_011531345.1:p.Ser272Ter
XM_011533044.1:c.812C>G	XP_011531346.1:p.Ser271Ter
XM_011533045.1:c.806C>G	XP_011531347.1:p.Ser269Ter
XM_011533046.1:c.*36C>G	XP_011531348.1:n.*36C>G
XM_005264502.2:c.830C>G	XP_005264559.1:p.Ser277Ter
XM_011533045.2:c.806C>G	XP_011531347.1:p.Ser269Ter
XM_017004725.1:c.815C>G	XP_016860214.1:p.Ser272Ter
XM_017004726.1:c.*36C>G	XP_016860215.1:n.*36C>G
XM_017004727.1:c.*36C>G	XP_016860216.1:n.*36C>G
NM_001164730.2:c.*36C>G	NP_001158202.1:n.*36C>G
NM_001164731.2:c.*36C>G	NP_001158203.1:n.*36C>G
NM_001164732.2:c.407C>G	NP_001158204.1:p.Ser136Ter
NM_001371279.1:c.830C>G MANE Select	NP_001358208.1:p.Ser277Ter
NM_001371280.1:c.464C>G	NP_001358209.1:p.Ser155Ter
NM_022912.3:c.*36C>G	NP_075063.1:n.*36C>G