Canonical Allele Identifier: CA914433792

Gene: REEP1

Linked Data

• dbSNP Id: rs1558862982
• gnomAD v2: 2-86444082-G-C
• gnomAD v3: 2-86216959-G-C
• gnomAD v4: 2-86216959-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86216959G>C , CM000664.2:g.86216959G>C	GRCh38
NC_000002.11:g.86444082G>C , CM000664.1:g.86444082G>C	GRCh37
NC_000002.10:g.86297593G>C	NCBI36
NG_013037.1:g.126125C>G , LRG_713:g.126125C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000643817.2:c.*80C>G	ENSP00000495610.2:n.*80C>G
ENST00000686220.1:c.*195C>G	ENSP00000509904.1:n.*195C>G
ENST00000687696.1:n.277C>G
ENST00000687927.1:n.1213C>G
ENST00000688400.1:c.435C>G	ENSP00000510490.1:n.435C>G
ENST00000689156.1:c.*80C>G	ENSP00000509143.1:n.*80C>G
ENST00000691093.1:c.*141C>G	ENSP00000509465.1:n.*141C>G
ENST00000691703.1:c.*141C>G	ENSP00000508496.1:n.*141C>G
ENST00000692664.1:c.*141C>G	ENSP00000508656.1:n.*141C>G
ENST00000693329.1:c.*221C>G	ENSP00000508490.1:n.*221C>G
ENST00000453231.6:c.*141C>G	ENSP00000392197.2:n.*141C>G
ENST00000535845.6:c.*141C>G	ENSP00000437567.1:n.*141C>G
ENST00000538924.7:c.*80C>G MANE Select	ENSP00000438346.3:n.*80C>G
ENST00000541910.6:c.*80C>G	ENSP00000442681.1:n.*80C>G
ENST00000642243.1:c.1043C>G	ENSP00000494960.1:n.1043C>G
ENST00000643817.1:c.857C>G	ENSP00000495610.1:n.857C>G
ENST00000644644.1:c.944C>G	ENSP00000494305.1:n.944C>G
ENST00000646181.1:n.620C>G
ENST00000165698.9:c.*141C>G	ENSP00000165698.5:n.*141C>G
ENST00000535845.5:c.*141C>G	ENSP00000437567.1:n.*141C>G
ENST00000538924.5:c.*141C>G	ENSP00000438346.1:n.*141C>G
ENST00000541910.5:c.*80C>G	ENSP00000442681.1:n.*80C>G
NM_001164730.1:c.*141C>G , LRG_713t1:c.*141C>G	NP_001158202.1:n.*141C>G
NM_001164731.1:c.*141C>G	NP_001158203.1:n.*141C>G
NM_001164732.1:c.*80C>G	NP_001158204.1:n.*80C>G
NM_022912.2:c.*141C>G , LRG_713t2:c.*141C>G	NP_075063.1:n.*141C>G
XM_005264502.1:c.*80C>G	XP_005264559.1:n.*80C>G
XM_005264504.1:c.*80C>G	XP_005264561.1:n.*80C>G
XM_011533043.1:c.*80C>G	XP_011531345.1:n.*80C>G
XM_011533044.1:c.*80C>G	XP_011531346.1:n.*80C>G
XM_011533045.1:c.*80C>G	XP_011531347.1:n.*80C>G
XM_005264502.2:c.*80C>G	XP_005264559.1:n.*80C>G
XM_011533045.2:c.*80C>G	XP_011531347.1:n.*80C>G
XM_017004725.1:c.*80C>G	XP_016860214.1:n.*80C>G
XM_017004726.1:c.*141C>G	XP_016860215.1:n.*141C>G
XM_017004727.1:c.*141C>G	XP_016860216.1:n.*141C>G
NM_001164730.2:c.*141C>G	NP_001158202.1:n.*141C>G
NM_001164731.2:c.*141C>G	NP_001158203.1:n.*141C>G
NM_001164732.2:c.*80C>G	NP_001158204.1:n.*80C>G
NM_001371279.1:c.*80C>G MANE Select	NP_001358208.1:n.*80C>G
NM_001371280.1:c.*80C>G	NP_001358209.1:n.*80C>G
NM_022912.3:c.*141C>G	NP_075063.1:n.*141C>G