Canonical Allele Identifier: CA2633583189

Gene: CNOT1

Linked Data

• gnomAD v4: 16-58533259-C-CGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.58533259_58533260insGG , CM000678.2:g.58533259_58533260insGG	GRCh38
NC_000016.9:g.58567163_58567164insGG , CM000678.1:g.58567163_58567164insGG	GRCh37
NC_000016.8:g.57124664_57124665insGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317147.10:c.5896-865_5896-864insCC MANE Select	ENSP00000320949.5:n.5896-865_5896-864insCC
ENST00000317147.9:c.5896-865_5896-864insCC	ENSP00000320949.5:n.5896-865_5896-864insCC
ENST00000567188.5:c.5881-865_5881-864insCC	ENSP00000456649.1:n.5881-865_5881-864insCC
ENST00000568917.1:c.1036-865_1036-864insCC	ENSP00000454611.1:n.1036-865_1036-864insCC
ENST00000569240.5:c.5881-865_5881-864insCC	ENSP00000455635.1:n.5881-865_5881-864insCC
NM_001265612.1:c.5881-865_5881-864insCC	NP_001252541.1:n.5881-865_5881-864insCC
NM_016284.4:c.5896-865_5896-864insCC	NP_057368.3:n.5896-865_5896-864insCC
NR_049763.1:n.6214-865_6214-864insCC
NM_016284.5:c.5896-865_5896-864insCC MANE Select	NP_057368.3:n.5896-865_5896-864insCC
NM_001265612.2:c.5881-865_5881-864insCC	NP_001252541.1:n.5881-865_5881-864insCC
NR_049763.2:n.6154-865_6154-864insCC