Canonical Allele Identifier: CA2633583051
Gene: CNOT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.58533176_58533177insGG , CM000678.2:g.58533176_58533177insGG GRCh38
NC_000016.9:g.58567080_58567081insGG , CM000678.1:g.58567080_58567081insGG GRCh37
NC_000016.8:g.57124581_57124582insGG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000317147.10:c.5896-782_5896-781insCC MANE Select ENSP00000320949.5:n.5896-782_5896-781insC...
ENST00000317147.9:c.5896-782_5896-781insCC ENSP00000320949.5:n.5896-782_5896-781insC...
ENST00000567188.5:c.5881-782_5881-781insCC ENSP00000456649.1:n.5881-782_5881-781insC...
ENST00000568917.1:c.1036-782_1036-781insCC ENSP00000454611.1:n.1036-782_1036-781insC...
ENST00000569240.5:c.5881-782_5881-781insCC ENSP00000455635.1:n.5881-782_5881-781insC...
NM_001265612.1:c.5881-782_5881-781insCC NP_001252541.1:n.5881-782_5881-781insCC
NM_016284.4:c.5896-782_5896-781insCC NP_057368.3:n.5896-782_5896-781insCC
NR_049763.1:n.6214-782_6214-781insCC
NM_016284.5:c.5896-782_5896-781insCC MANE Select NP_057368.3:n.5896-782_5896-781insCC
NM_001265612.2:c.5881-782_5881-781insCC NP_001252541.1:n.5881-782_5881-781insCC
NR_049763.2:n.6154-782_6154-781insCC