Canonical Allele Identifier: CA2932580

Gene: REST

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.56931767T>A , CM000666.2:g.56931767T>A	GRCh38
NC_000004.11:g.57797933T>A , CM000666.1:g.57797933T>A	GRCh37
NC_000004.10:g.57492690T>A	NCBI36
NG_029447.1:g.28892T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309042.12:c.2909T>A MANE Select	ENSP00000311816.7:p.Val970Asp
ENST00000514063.2:c.*1936T>A	ENSP00000501649.1:n.*1936T>A
ENST00000611211.2:c.*79-301T>A	ENSP00000479151.2:n.*79-301T>A
ENST00000616975.5:c.*1936T>A	ENSP00000484058.1:n.*1936T>A
ENST00000619101.5:c.*1936T>A	ENSP00000484836.2:n.*1936T>A
ENST00000638187.2:c.2825T>A	ENSP00000492006.2:p.Val942Asp
ENST00000640168.2:c.898+20231T>A	ENSP00000490969.1:n.898+20231T>A
ENST00000640343.2:c.982+11897T>A	ENSP00000492813.1:n.982+11897T>A
ENST00000675105.1:c.2909T>A	ENSP00000502313.1:p.Val970Asp
ENST00000675341.1:c.2462T>A	ENSP00000502488.1:p.Val821Asp
ENST00000309042.11:c.2909T>A	ENSP00000311816.7:p.Val970Asp
ENST00000619101.4:c.2909T>A	ENSP00000484836.1:p.Val970Asp
ENST00000622863.4:c.587-27T>A	ENSP00000481650.1:n.587-27T>A
NM_001193508.1:c.2909T>A	NP_001180437.1:p.Val970Asp
NM_005612.4:c.2909T>A	NP_005603.3:p.Val970Asp
XM_005265760.2:c.1943T>A	XP_005265817.1:p.Val648Asp
XM_011534401.1:c.2909T>A	XP_011532703.1:p.Val970Asp
XM_011534402.1:c.1931T>A	XP_011532704.1:p.Val644Asp
NM_001363453.1:c.2909T>A	NP_001350382.1:p.Val970Asp
XM_017008527.1:c.2825T>A	XP_016864016.1:p.Val942Asp
NM_005612.5:c.2909T>A MANE Select	NP_005603.3:p.Val970Asp
NM_001363453.2:c.2909T>A	NP_001350382.1:p.Val970Asp