Canonical Allele Identifier: CA1459755541
Gene: REST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.56920212A= , CM000666.2:g.56920212A= GRCh38
NC_000004.11:g.57786378A= , CM000666.1:g.57786378A= GRCh37
NC_000004.10:g.57481135A= NCBI36
NG_029447.1:g.17337A=

Transcript Alleles

HGVS Amino-acid change
ENST00000309042.12:c.982+342A= MANE Select ENSP00000311816.7:n.982+342A=
ENST00000514063.2:c.982+342A= ENSP00000501649.1:n.982+342A=
ENST00000611211.2:c.982+342A= ENSP00000479151.2:n.982+342A=
ENST00000616975.5:c.982+342A= ENSP00000484058.1:n.982+342A=
ENST00000619101.5:c.982+342A= ENSP00000484836.2:n.982+342A=
ENST00000638187.2:c.898+8676A= ENSP00000492006.2:n.898+8676A=
ENST00000640168.2:c.898+8676A= ENSP00000490969.1:n.898+8676A=
ENST00000640343.2:c.982+342A= ENSP00000492813.1:n.982+342A=
ENST00000675105.1:c.982+342A= ENSP00000502313.1:n.982+342A=
ENST00000675341.1:c.535+342A= ENSP00000502488.1:n.535+342A=
ENST00000309042.11:c.982+342A= ENSP00000311816.7:n.982+342A=
ENST00000514063.1:n.409+342A=
ENST00000611211.1:c.982+342A= ENSP00000479151.1:n.982+342A=
ENST00000612429.4:c.982+342A= ENSP00000484206.1:n.982+342A=
ENST00000616975.4:c.982+342A= ENSP00000484058.1:n.982+342A=
ENST00000619101.4:c.982+342A= ENSP00000484836.1:n.982+342A=
ENST00000622863.4:c.586+342A= ENSP00000481650.1:n.586+342A=
NM_001193508.1:c.982+342A= NP_001180437.1:n.982+342A=
NM_005612.4:c.982+342A= NP_005603.3:n.982+342A=
XM_005265760.2:c.16+342A= XP_005265817.1:n.16+342A=
XM_011534401.1:c.982+342A= XP_011532703.1:n.982+342A=
NM_001363453.1:c.982+342A= NP_001350382.1:n.982+342A=
XM_017008527.1:c.898+8676A= XP_016864016.1:n.898+8676A=
NM_005612.5:c.982+342A= MANE Select NP_005603.3:n.982+342A=
NM_001363453.2:c.982+342A= NP_001350382.1:n.982+342A=