Canonical Allele Identifier: CA977770981

Gene: CNOT1

Linked Data

• dbSNP Id: rs2039824087
• gnomAD v3: 16-58533267-G-A
• gnomAD v4: 16-58533267-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.58533267G>A , CM000678.2:g.58533267G>A	GRCh38
NC_000016.9:g.58567171G>A , CM000678.1:g.58567171G>A	GRCh37
NC_000016.8:g.57124672G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000317147.10:c.5896-872C>T MANE Select	ENSP00000320949.5:n.5896-872C>T
ENST00000317147.9:c.5896-872C>T	ENSP00000320949.5:n.5896-872C>T
ENST00000567188.5:c.5881-872C>T	ENSP00000456649.1:n.5881-872C>T
ENST00000568917.1:c.1036-872C>T	ENSP00000454611.1:n.1036-872C>T
ENST00000569240.5:c.5881-872C>T	ENSP00000455635.1:n.5881-872C>T
NM_001265612.1:c.5881-872C>T	NP_001252541.1:n.5881-872C>T
NM_016284.4:c.5896-872C>T	NP_057368.3:n.5896-872C>T
NR_049763.1:n.6214-872C>T
NM_016284.5:c.5896-872C>T MANE Select	NP_057368.3:n.5896-872C>T
NM_001265612.2:c.5881-872C>T	NP_001252541.1:n.5881-872C>T
NR_049763.2:n.6154-872C>T