Canonical Allele Identifier: CA2633583148
Gene: CNOT1 HGNC NCBI

Linked Data

gnomAD v4: 16-58533236-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.58533236G>T , CM000678.2:g.58533236G>T GRCh38
NC_000016.9:g.58567140G>T , CM000678.1:g.58567140G>T GRCh37
NC_000016.8:g.57124641G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000317147.10:c.5896-841C>A MANE Select ENSP00000320949.5:n.5896-841C>A
ENST00000317147.9:c.5896-841C>A ENSP00000320949.5:n.5896-841C>A
ENST00000567188.5:c.5881-841C>A ENSP00000456649.1:n.5881-841C>A
ENST00000568917.1:c.1036-841C>A ENSP00000454611.1:n.1036-841C>A
ENST00000569240.5:c.5881-841C>A ENSP00000455635.1:n.5881-841C>A
NM_001265612.1:c.5881-841C>A NP_001252541.1:n.5881-841C>A
NM_016284.4:c.5896-841C>A NP_057368.3:n.5896-841C>A
NR_049763.1:n.6214-841C>A
NM_016284.5:c.5896-841C>A MANE Select NP_057368.3:n.5896-841C>A
NM_001265612.2:c.5881-841C>A NP_001252541.1:n.5881-841C>A
NR_049763.2:n.6154-841C>A
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