Canonical Allele Identifier: CA2633582972

Gene: CNOT1

Linked Data

• gnomAD v4: 16-58533127-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.58533127C>T , CM000678.2:g.58533127C>T	GRCh38
NC_000016.9:g.58567031C>T , CM000678.1:g.58567031C>T	GRCh37
NC_000016.8:g.57124532C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317147.10:c.5896-732G>A MANE Select	ENSP00000320949.5:n.5896-732G>A
ENST00000317147.9:c.5896-732G>A	ENSP00000320949.5:n.5896-732G>A
ENST00000563130.5:n.39G>A
ENST00000567188.5:c.5881-732G>A	ENSP00000456649.1:n.5881-732G>A
ENST00000568917.1:c.1036-732G>A	ENSP00000454611.1:n.1036-732G>A
ENST00000569240.5:c.5881-732G>A	ENSP00000455635.1:n.5881-732G>A
NM_001265612.1:c.5881-732G>A	NP_001252541.1:n.5881-732G>A
NM_016284.4:c.5896-732G>A	NP_057368.3:n.5896-732G>A
NR_049763.1:n.6214-732G>A
NM_016284.5:c.5896-732G>A MANE Select	NP_057368.3:n.5896-732G>A
NM_001265612.2:c.5881-732G>A	NP_001252541.1:n.5881-732G>A
NR_049763.2:n.6154-732G>A