Canonical Allele Identifier: CA281675326
Gene: CNOT1 HGNC NCBI

Linked Data

dbSNP Id: rs34946544
MyVariant Identifiers: chr16:g.58567164_58567165insG (hg19) chr16:g.58533260_58533261insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.58533262dup , CM000678.2:g.58533262dup GRCh38
NC_000016.9:g.58567166dup , CM000678.1:g.58567166dup GRCh37
NC_000016.8:g.57124667dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000317147.10:c.5896-866dup MANE Select ENSP00000320949.5:n.5896-866dup
ENST00000317147.9:c.5896-866dup ENSP00000320949.5:n.5896-866dup
ENST00000567188.5:c.5881-866dup ENSP00000456649.1:n.5881-866dup
ENST00000568917.1:c.1036-866dup ENSP00000454611.1:n.1036-866dup
ENST00000569240.5:c.5881-866dup ENSP00000455635.1:n.5881-866dup
NM_001265612.1:c.5881-866dup NP_001252541.1:n.5881-866dup
NM_016284.4:c.5896-866dup NP_057368.3:n.5896-866dup
NR_049763.1:n.6214-866dup
NM_016284.5:c.5896-866dup MANE Select NP_057368.3:n.5896-866dup
NM_001265612.2:c.5881-866dup NP_001252541.1:n.5881-866dup
NR_049763.2:n.6154-866dup
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