Canonical Allele Identifier: CA1604701077

Gene: CNOT6

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180578337T= , CM000667.2:g.180578337T=	GRCh38
NC_000005.9:g.180005337T= , CM000667.1:g.180005337T=	GRCh37
NC_000005.8:g.179937943T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261951.9:c.*4137T= MANE Select	ENSP00000261951.4:n.*4137T=
ENST00000393356.7:c.*4137T=	ENSP00000377024.1:n.*4137T=
ENST00000261951.8:c.*4137T=	ENSP00000261951.4:n.*4137T=
ENST00000393356.5:c.*4137T=	ENSP00000377024.1:n.*4137T=
ENST00000618123.4:c.*4137T=	ENSP00000481893.1:n.*4137T=
NM_001303241.1:c.*4137T=	NP_001290170.1:n.*4137T=
XM_005265953.1:c.*4137T=	XP_005266010.1:n.*4137T=
XM_011534605.1:c.*4137T=	XP_011532907.1:n.*4137T=
XM_011534606.1:c.*4137T=	XP_011532908.1:n.*4137T=
XM_011534607.1:c.*4137T=	XP_011532909.1:n.*4137T=
XM_011534608.1:c.*4321T=	XP_011532910.1:n.*4321T=
XM_017009672.1:c.*4321T=	XP_016865161.1:n.*4321T=
XR_001742163.1:n.6022T=
XR_001742164.1:n.6007T=
NM_001303241.2:c.*4137T=	NP_001290170.1:n.*4137T=
NM_001370472.1:c.*4137T= MANE Select	NP_001357401.1:n.*4137T=
NM_001370473.1:c.*4137T=	NP_001357402.1:n.*4137T=
NM_001370474.1:c.*4137T=	NP_001357403.1:n.*4137T=
NR_163437.1:n.6302T=
NR_163438.1:n.6043T=