Canonical Allele Identifier: CA15304290

Gene: REST

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.56910349G>A , CM000666.2:g.56910349G>A	GRCh38
NC_000004.11:g.57776515G>A , CM000666.1:g.57776515G>A	GRCh37
NC_000004.10:g.57471272G>A	NCBI36
NG_029447.1:g.7474G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309042.12:c.-9-281G>A MANE Select	ENSP00000311816.7:n.-9-281G>A
ENST00000514063.2:c.-9-281G>A	ENSP00000501649.1:n.-9-281G>A
ENST00000611211.2:c.-9-281G>A	ENSP00000479151.2:n.-9-281G>A
ENST00000616975.5:c.-9-281G>A	ENSP00000484058.1:n.-9-281G>A
ENST00000619101.5:c.-9-281G>A	ENSP00000484836.2:n.-9-281G>A
ENST00000638187.2:c.-9-281G>A	ENSP00000492006.2:n.-9-281G>A
ENST00000640168.2:c.-9-281G>A	ENSP00000490969.1:n.-9-281G>A
ENST00000640343.2:c.-9-281G>A	ENSP00000492813.1:n.-9-281G>A
ENST00000675105.1:c.-9-281G>A	ENSP00000502313.1:n.-9-281G>A
ENST00000675341.1:c.-9-281G>A	ENSP00000502488.1:n.-9-281G>A
ENST00000309042.11:c.-9-281G>A	ENSP00000311816.7:n.-9-281G>A
ENST00000503522.1:n.399-281G>A
ENST00000511065.5:n.128-281G>A
ENST00000611211.1:c.-9-281G>A	ENSP00000479151.1:n.-9-281G>A
ENST00000612429.4:c.-9-281G>A	ENSP00000484206.1:n.-9-281G>A
ENST00000616975.4:c.-9-281G>A	ENSP00000484058.1:n.-9-281G>A
ENST00000619101.4:c.-9-281G>A	ENSP00000484836.1:n.-9-281G>A
ENST00000622863.4:c.-9-281G>A	ENSP00000481650.1:n.-9-281G>A
NM_001193508.1:c.-9-281G>A	NP_001180437.1:n.-9-281G>A
NM_005612.4:c.-9-281G>A	NP_005603.3:n.-9-281G>A
XM_005265760.2:c.-175+2136G>A	XP_005265817.1:n.-175+2136G>A
XM_011534401.1:c.-9-281G>A	XP_011532703.1:n.-9-281G>A
NM_001363453.1:c.-9-281G>A	NP_001350382.1:n.-9-281G>A
XM_017008527.1:c.-9-281G>A	XP_016864016.1:n.-9-281G>A
NM_005612.5:c.-9-281G>A MANE Select	NP_005603.3:n.-9-281G>A
NM_001363453.2:c.-9-281G>A	NP_001350382.1:n.-9-281G>A