Canonical Allele Identifier: CA14221847

Gene: CNOT1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.58588274G>A , CM000678.2:g.58588274G>A	GRCh38
NC_000016.9:g.58622178G>A , CM000678.1:g.58622178G>A	GRCh37
NC_000016.8:g.57179679G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317147.10:c.211-396C>T MANE Select	ENSP00000320949.5:n.211-396C>T
ENST00000317147.9:c.211-396C>T	ENSP00000320949.5:n.211-396C>T
ENST00000441024.6:c.211-396C>T	ENSP00000413113.2:n.211-396C>T
ENST00000565605.5:c.211-396C>T	ENSP00000457460.1:n.211-396C>T
ENST00000567188.5:c.211-396C>T	ENSP00000456649.1:n.211-396C>T
ENST00000569240.5:c.211-396C>T	ENSP00000455635.1:n.211-396C>T
ENST00000628857.1:c.211-396C>T	ENSP00000485782.1:n.211-396C>T
NM_001265612.1:c.211-396C>T	NP_001252541.1:n.211-396C>T
NM_016284.4:c.211-396C>T	NP_057368.3:n.211-396C>T
NM_206999.2:c.211-396C>T	NP_996882.1:n.211-396C>T
NR_049763.1:n.544-396C>T
NM_016284.5:c.211-396C>T MANE Select	NP_057368.3:n.211-396C>T
NM_001265612.2:c.211-396C>T	NP_001252541.1:n.211-396C>T
NM_206999.3:c.211-396C>T	NP_996882.1:n.211-396C>T
NR_049763.2:n.484-396C>T