Canonical Allele Identifier: CA323435

Gene: REEP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86232673C>T , CM000664.2:g.86232673C>T	GRCh38
NC_000002.11:g.86459796C>T , CM000664.1:g.86459796C>T	GRCh37
NC_000002.10:g.86313307C>T	NCBI36
NG_013037.1:g.110411G>A , LRG_713:g.110411G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001371279.1:c.547G>A MANE Select	NP_001358208.1:p.Gly183Ser
ENST00000538924.7:c.547G>A MANE Select	ENSP00000438346.3:p.Gly183Ser
NM_001164730.1:c.568G>A , LRG_713t1:c.568G>A	NP_001158202.1:p.Gly190Ser
NM_001164730.2:c.568G>A	NP_001158202.1:p.Gly190Ser
NM_001164731.1:c.466G>A	NP_001158203.1:p.Gly156Ser
NM_001164731.2:c.466G>A	NP_001158203.1:p.Gly156Ser
NM_001164732.1:c.312G>A	NP_001158204.1:p.Thr104=
NM_001164732.2:c.312G>A	NP_001158204.1:p.Thr104=
NM_001371280.1:c.418-15563G>A	NP_001358209.1:n.418-15563G>A
NM_022912.2:c.547G>A , LRG_713t2:c.547G>A	NP_075063.1:p.Gly183Ser
NM_022912.3:c.547G>A	NP_075063.1:p.Gly183Ser
ENST00000165698.9:c.547G>A	ENSP00000165698.5:p.Gly183Ser
ENST00000437769.5:c.312G>A	ENSP00000401140.1:p.Thr104=
ENST00000453231.5:c.568G>A	ENSP00000392197.1:p.Gly190Ser
ENST00000453231.6:c.568G>A	ENSP00000392197.2:p.Gly190Ser
ENST00000535845.5:c.466G>A	ENSP00000437567.1:p.Gly156Ser
ENST00000535845.6:c.466G>A	ENSP00000437567.1:p.Gly156Ser
ENST00000538924.5:c.568G>A	ENSP00000438346.1:p.Gly190Ser
ENST00000541910.5:c.312G>A	ENSP00000442681.1:p.Thr104=
ENST00000541910.6:c.312G>A	ENSP00000442681.1:p.Thr104=
ENST00000642243.1:c.655G>A	ENSP00000494960.1:p.Gly219Ser
ENST00000643817.1:c.505G>A	ENSP00000495610.1:p.Gly169Ser
ENST00000643817.2:c.547G>A	ENSP00000495610.2:p.Gly183Ser
ENST00000644644.1:c.556G>A	ENSP00000494305.1:p.Gly186Ser
ENST00000686220.1:c.466G>A	ENSP00000509904.1:p.Gly156Ser
ENST00000688400.1:c.235G>A	ENSP00000510490.1:p.Gly79Ser
ENST00000689156.1:c.418-15563G>A	ENSP00000509143.1:n.418-15563G>A
ENST00000691093.1:c.367G>A	ENSP00000509465.1:p.Gly123Ser
ENST00000691703.1:c.547G>A	ENSP00000508496.1:p.Gly183Ser
ENST00000692664.1:c.397G>A	ENSP00000508656.1:p.Gly133Ser
ENST00000693329.1:c.547G>A	ENSP00000508490.1:p.Gly183Ser
XM_005264502.1:c.547G>A	XP_005264559.1:p.Gly183Ser
XM_005264502.2:c.547G>A	XP_005264559.1:p.Gly183Ser
XM_005264504.1:c.433G>A	XP_005264561.1:p.Gly145Ser
XM_011533043.1:c.568G>A	XP_011531345.1:p.Gly190Ser
XM_011533044.1:c.529G>A	XP_011531346.1:p.Gly177Ser
XM_011533045.1:c.523G>A	XP_011531347.1:p.Gly175Ser
XM_011533045.2:c.523G>A	XP_011531347.1:p.Gly175Ser
XM_011533046.1:c.568G>A	XP_011531348.1:p.Gly190Ser
XM_017004725.1:c.568G>A	XP_016860214.1:p.Gly190Ser
XM_017004726.1:c.568G>A	XP_016860215.1:p.Gly190Ser
XM_017004727.1:c.568G>A	XP_016860216.1:p.Gly190Ser