Canonical Allele Identifier: CA796544118

Gene: REST

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.56927585G>T , CM000666.2:g.56927585G>T	GRCh38
NC_000004.11:g.57793751G>T , CM000666.1:g.57793751G>T	GRCh37
NC_000004.10:g.57488508G>T	NCBI36
NG_029447.1:g.24710G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309042.12:c.983-2256G>T MANE Select	ENSP00000311816.7:n.983-2256G>T
ENST00000514063.2:c.983-30G>T	ENSP00000501649.1:n.983-30G>T
ENST00000611211.2:c.*79-4483G>T	ENSP00000479151.2:n.*79-4483G>T
ENST00000616975.5:c.983-30G>T	ENSP00000484058.1:n.983-30G>T
ENST00000619101.5:c.983-30G>T	ENSP00000484836.2:n.983-30G>T
ENST00000638187.2:c.899-2256G>T	ENSP00000492006.2:n.899-2256G>T
ENST00000640168.2:c.898+16049G>T	ENSP00000490969.1:n.898+16049G>T
ENST00000640343.2:c.982+7715G>T	ENSP00000492813.1:n.982+7715G>T
ENST00000675105.1:c.983-2256G>T	ENSP00000502313.1:n.983-2256G>T
ENST00000675341.1:c.536-2256G>T	ENSP00000502488.1:n.536-2256G>T
ENST00000309042.11:c.983-2256G>T	ENSP00000311816.7:n.983-2256G>T
ENST00000514063.1:n.410-30G>T
ENST00000611211.1:c.983-30G>T	ENSP00000479151.1:n.983-30G>T
ENST00000616975.4:c.983-30G>T	ENSP00000484058.1:n.983-30G>T
ENST00000619101.4:c.983-2256G>T	ENSP00000484836.1:n.983-2256G>T
ENST00000622863.4:c.587-4209G>T	ENSP00000481650.1:n.587-4209G>T
NM_001193508.1:c.983-2256G>T	NP_001180437.1:n.983-2256G>T
NM_005612.4:c.983-2256G>T	NP_005603.3:n.983-2256G>T
XM_005265760.2:c.17-2256G>T	XP_005265817.1:n.17-2256G>T
XM_011534401.1:c.983-2256G>T	XP_011532703.1:n.983-2256G>T
NM_001363453.1:c.983-2256G>T	NP_001350382.1:n.983-2256G>T
XM_017008527.1:c.899-2256G>T	XP_016864016.1:n.899-2256G>T
NM_005612.5:c.983-2256G>T MANE Select	NP_005603.3:n.983-2256G>T
NM_001363453.2:c.983-2256G>T	NP_001350382.1:n.983-2256G>T