Canonical Allele Identifier: CA2225119761
Gene: CNOT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.58533204C= , CM000678.2:g.58533204C= GRCh38
NC_000016.9:g.58567108C= , CM000678.1:g.58567108C= GRCh37
NC_000016.8:g.57124609C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000317147.10:c.5896-809G= MANE Select ENSP00000320949.5:n.5896-809G=
ENST00000317147.9:c.5896-809G= ENSP00000320949.5:n.5896-809G=
ENST00000567188.5:c.5881-809G= ENSP00000456649.1:n.5881-809G=
ENST00000568917.1:c.1036-809G= ENSP00000454611.1:n.1036-809G=
ENST00000569240.5:c.5881-809G= ENSP00000455635.1:n.5881-809G=
NM_001265612.1:c.5881-809G= NP_001252541.1:n.5881-809G=
NM_016284.4:c.5896-809G= NP_057368.3:n.5896-809G=
NR_049763.1:n.6214-809G=
NM_016284.5:c.5896-809G= MANE Select NP_057368.3:n.5896-809G=
NM_001265612.2:c.5881-809G= NP_001252541.1:n.5881-809G=
NR_049763.2:n.6154-809G=
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