Canonical Allele Identifier: CA439508860

Gene: REST

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.56911496C>T , CM000666.2:g.56911496C>T	GRCh38
NC_000004.11:g.57777662C>T , CM000666.1:g.57777662C>T	GRCh37
NC_000004.10:g.57472419C>T	NCBI36
NG_029447.1:g.8621C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005612.5:c.858C>T MANE Select	NP_005603.3:p.Asp286=
ENST00000309042.12:c.858C>T MANE Select	ENSP00000311816.7:p.Asp286=
NM_001193508.1:c.858C>T	NP_001180437.1:p.Asp286=
NM_001363453.1:c.858C>T	NP_001350382.1:p.Asp286=
NM_001363453.2:c.858C>T	NP_001350382.1:p.Asp286=
NM_005612.4:c.858C>T	NP_005603.3:p.Asp286=
ENST00000309042.11:c.858C>T	ENSP00000311816.7:p.Asp286=
ENST00000514063.1:n.285C>T
ENST00000514063.2:c.858C>T	ENSP00000501649.1:p.Asp286=
ENST00000611211.1:c.858C>T	ENSP00000479151.1:p.Asp286=
ENST00000611211.2:c.858C>T	ENSP00000479151.2:p.Asp286=
ENST00000612429.4:c.858C>T	ENSP00000484206.1:p.Asp286=
ENST00000616975.4:c.858C>T	ENSP00000484058.1:p.Asp286=
ENST00000616975.5:c.858C>T	ENSP00000484058.1:p.Asp286=
ENST00000619101.4:c.858C>T	ENSP00000484836.1:p.Asp286=
ENST00000619101.5:c.858C>T	ENSP00000484836.2:p.Asp286=
ENST00000622863.4:c.462C>T	ENSP00000481650.1:p.Asp154=
ENST00000638187.2:c.858C>T	ENSP00000492006.2:p.Asp286=
ENST00000640168.2:c.858C>T	ENSP00000490969.1:p.Asp286=
ENST00000640343.2:c.858C>T	ENSP00000492813.1:p.Asp286=
ENST00000675105.1:c.858C>T	ENSP00000502313.1:p.Asp286=
ENST00000675341.1:c.451+407C>T	ENSP00000502488.1:n.451+407C>T
XM_005265760.2:c.-175+3283C>T	XP_005265817.1:n.-175+3283C>T
XM_011534401.1:c.858C>T	XP_011532703.1:p.Asp286=
XM_017008527.1:c.858C>T	XP_016864016.1:p.Asp286=