Canonical Allele Identifier: CA2932354

Gene: REST

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.56930791C>T , CM000666.2:g.56930791C>T	GRCh38
NC_000004.11:g.57796957C>T , CM000666.1:g.57796957C>T	GRCh37
NC_000004.10:g.57491714C>T	NCBI36
NG_029447.1:g.27916C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309042.12:c.1933C>T MANE Select	ENSP00000311816.7:p.Arg645Trp
ENST00000514063.2:c.*960C>T	ENSP00000501649.1:n.*960C>T
ENST00000611211.2:c.*79-1277C>T	ENSP00000479151.2:n.*79-1277C>T
ENST00000616975.5:c.*960C>T	ENSP00000484058.1:n.*960C>T
ENST00000619101.5:c.*960C>T	ENSP00000484836.2:n.*960C>T
ENST00000638187.2:c.1849C>T	ENSP00000492006.2:p.Arg617Trp
ENST00000640168.2:c.898+19255C>T	ENSP00000490969.1:n.898+19255C>T
ENST00000640343.2:c.982+10921C>T	ENSP00000492813.1:n.982+10921C>T
ENST00000675105.1:c.1933C>T	ENSP00000502313.1:p.Arg645Trp
ENST00000675341.1:c.1486C>T	ENSP00000502488.1:p.Arg496Trp
ENST00000309042.11:c.1933C>T	ENSP00000311816.7:p.Arg645Trp
ENST00000619101.4:c.1933C>T	ENSP00000484836.1:p.Arg645Trp
ENST00000622863.4:c.587-1003C>T	ENSP00000481650.1:n.587-1003C>T
NM_001193508.1:c.1933C>T	NP_001180437.1:p.Arg645Trp
NM_005612.4:c.1933C>T	NP_005603.3:p.Arg645Trp
XM_005265760.2:c.967C>T	XP_005265817.1:p.Arg323Trp
XM_011534401.1:c.1933C>T	XP_011532703.1:p.Arg645Trp
XM_011534402.1:c.955C>T	XP_011532704.1:p.Arg319Trp
NM_001363453.1:c.1933C>T	NP_001350382.1:p.Arg645Trp
XM_017008527.1:c.1849C>T	XP_016864016.1:p.Arg617Trp
NM_005612.5:c.1933C>T MANE Select	NP_005603.3:p.Arg645Trp
NM_001363453.2:c.1933C>T	NP_001350382.1:p.Arg645Trp