Canonical Allele Identifier: CA2932437

Gene: REST

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.56931117_56931164del , CM000666.2:g.56931117_56931164del	GRCh38
NC_000004.11:g.57797283_57797330del , CM000666.1:g.57797283_57797330del	GRCh37
NC_000004.10:g.57492040_57492087del	NCBI36
NG_029447.1:g.28242_28289del

Transcript Alleles

HGVS	Amino-acid Change
NM_005612.5:c.2259_2306del MANE Select	NP_005603.3:p.Met753_Pro768del
ENST00000309042.12:c.2259_2306del MANE Select	ENSP00000311816.7:p.Met753_Pro768del
NM_001193508.1:c.2259_2306del	NP_001180437.1:p.Met753_Pro768del
NM_001363453.1:c.2259_2306del	NP_001350382.1:p.Met753_Pro768del
NM_001363453.2:c.2259_2306del	NP_001350382.1:p.Met753_Pro768del
NM_005612.4:c.2259_2306del	NP_005603.3:p.Met753_Pro768del
ENST00000309042.11:c.2259_2306del	ENSP00000311816.7:p.Met753_Pro768del
ENST00000514063.2:c.*1286_*1333del	ENSP00000501649.1:n.*1286_*1333del
ENST00000611211.2:c.*79-951_*79-904del	ENSP00000479151.2:n.*79-951_*79-904del
ENST00000616975.5:c.*1286_*1333del	ENSP00000484058.1:n.*1286_*1333del
ENST00000619101.4:c.2259_2306del	ENSP00000484836.1:p.Met753_Pro768del
ENST00000619101.5:c.*1286_*1333del	ENSP00000484836.2:n.*1286_*1333del
ENST00000622863.4:c.587-677_587-630del	ENSP00000481650.1:n.587-677_587-630del
ENST00000638187.2:c.2175_2222del	ENSP00000492006.2:p.Met725_Pro740del
ENST00000640168.2:c.898+19581_898+19628del	ENSP00000490969.1:n.898+19581_898+19628del
ENST00000640343.2:c.982+11247_982+11294del	ENSP00000492813.1:n.982+11247_982+11294del
ENST00000675105.1:c.2259_2306del	ENSP00000502313.1:p.Met753_Pro768del
ENST00000675341.1:c.1812_1859del	ENSP00000502488.1:p.Met604_Pro619del
XM_005265760.2:c.1293_1340del	XP_005265817.1:p.Met431_Pro446del
XM_011534401.1:c.2259_2306del	XP_011532703.1:p.Met753_Pro768del
XM_011534402.1:c.1281_1328del	XP_011532704.1:p.Met427_Pro442del
XM_017008527.1:c.2175_2222del	XP_016864016.1:p.Met725_Pro740del