Canonical Allele Identifier: CA2225119839

Gene: CNOT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.58533364C= , CM000678.2:g.58533364C=	GRCh38
NC_000016.9:g.58567268C= , CM000678.1:g.58567268C=	GRCh37
NC_000016.8:g.57124769C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000317147.10:c.5895+783G= MANE Select	ENSP00000320949.5:n.5895+783G=
ENST00000317147.9:c.5895+783G=	ENSP00000320949.5:n.5895+783G=
ENST00000567188.5:c.5880+783G=	ENSP00000456649.1:n.5880+783G=
ENST00000568917.1:c.1035+783G=	ENSP00000454611.1:n.1035+783G=
ENST00000569240.5:c.5880+783G=	ENSP00000455635.1:n.5880+783G=
NM_001265612.1:c.5880+783G=	NP_001252541.1:n.5880+783G=
NM_016284.4:c.5895+783G=	NP_057368.3:n.5895+783G=
NR_049763.1:n.6213+783G=
NM_016284.5:c.5895+783G= MANE Select	NP_057368.3:n.5895+783G=
NM_001265612.2:c.5880+783G=	NP_001252541.1:n.5880+783G=
NR_049763.2:n.6153+783G=