Canonical Allele Identifier: CA347544140

Gene: REEP1

Linked Data

• MyVariant Identifiers: chr2:g.86444175G>C (hg19) ; chr2:g.86217052G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86217052G>C , CM000664.2:g.86217052G>C	GRCh38
NC_000002.11:g.86444175G>C , CM000664.1:g.86444175G>C	GRCh37
NC_000002.10:g.86297686G>C	NCBI36
NG_013037.1:g.126032C>G , LRG_713:g.126032C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000643817.2:c.806C>G	ENSP00000495610.2:p.Thr269Ser
ENST00000686220.1:c.*102C>G	ENSP00000509904.1:n.*102C>G
ENST00000687696.1:n.184C>G
ENST00000687927.1:n.1120C>G
ENST00000688400.1:c.342C>G	ENSP00000510490.1:n.342C>G
ENST00000689156.1:c.476C>G	ENSP00000509143.1:p.Thr159Ser
ENST00000691093.1:c.*48C>G	ENSP00000509465.1:n.*48C>G
ENST00000691703.1:c.*48C>G	ENSP00000508496.1:n.*48C>G
ENST00000692664.1:c.*48C>G	ENSP00000508656.1:n.*48C>G
ENST00000693329.1:c.*128C>G	ENSP00000508490.1:n.*128C>G
ENST00000453231.6:c.*48C>G	ENSP00000392197.2:n.*48C>G
ENST00000535845.6:c.*48C>G	ENSP00000437567.1:n.*48C>G
ENST00000538924.7:c.842C>G MANE Select	ENSP00000438346.3:p.Thr281Ser
ENST00000541910.6:c.419C>G	ENSP00000442681.1:p.Thr140Ser
ENST00000642243.1:c.950C>G	ENSP00000494960.1:p.Thr317Ser
ENST00000643817.1:c.764C>G	ENSP00000495610.1:p.Thr255Ser
ENST00000644644.1:c.851C>G	ENSP00000494305.1:p.Thr284Ser
ENST00000646181.1:n.527C>G
ENST00000165698.9:c.*48C>G	ENSP00000165698.5:n.*48C>G
ENST00000535845.5:c.*48C>G	ENSP00000437567.1:n.*48C>G
ENST00000538924.5:c.*48C>G	ENSP00000438346.1:n.*48C>G
ENST00000541910.5:c.419C>G	ENSP00000442681.1:p.Thr140Ser
NM_001164730.1:c.*48C>G , LRG_713t1:c.*48C>G	NP_001158202.1:n.*48C>G
NM_001164731.1:c.*48C>G	NP_001158203.1:n.*48C>G
NM_001164732.1:c.419C>G	NP_001158204.1:p.Thr140Ser
NM_022912.2:c.*48C>G , LRG_713t2:c.*48C>G	NP_075063.1:n.*48C>G
XM_005264502.1:c.842C>G	XP_005264559.1:p.Thr281Ser
XM_005264504.1:c.728C>G	XP_005264561.1:p.Thr243Ser
XM_011533043.1:c.827C>G	XP_011531345.1:p.Thr276Ser
XM_011533044.1:c.824C>G	XP_011531346.1:p.Thr275Ser
XM_011533045.1:c.818C>G	XP_011531347.1:p.Thr273Ser
XM_011533046.1:c.*48C>G	XP_011531348.1:n.*48C>G
XM_005264502.2:c.842C>G	XP_005264559.1:p.Thr281Ser
XM_011533045.2:c.818C>G	XP_011531347.1:p.Thr273Ser
XM_017004725.1:c.827C>G	XP_016860214.1:p.Thr276Ser
XM_017004726.1:c.*48C>G	XP_016860215.1:n.*48C>G
XM_017004727.1:c.*48C>G	XP_016860216.1:n.*48C>G
NM_001164730.2:c.*48C>G	NP_001158202.1:n.*48C>G
NM_001164731.2:c.*48C>G	NP_001158203.1:n.*48C>G
NM_001164732.2:c.419C>G	NP_001158204.1:p.Thr140Ser
NM_001371279.1:c.842C>G MANE Select	NP_001358208.1:p.Thr281Ser
NM_001371280.1:c.476C>G	NP_001358209.1:p.Thr159Ser
NM_022912.3:c.*48C>G	NP_075063.1:n.*48C>G