Canonical Allele Identifier: CA1604701081

Gene: CNOT6

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180578356A= , CM000667.2:g.180578356A=	GRCh38
NC_000005.9:g.180005356A= , CM000667.1:g.180005356A=	GRCh37
NC_000005.8:g.179937962A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261951.9:c.*4156A= MANE Select	ENSP00000261951.4:n.*4156A=
ENST00000393356.5:c.*4156A=	ENSP00000377024.1:n.*4156A=
NM_001303241.1:c.*4156A=	NP_001290170.1:n.*4156A=
XM_005265953.1:c.*4156A=	XP_005266010.1:n.*4156A=
XM_011534605.1:c.*4156A=	XP_011532907.1:n.*4156A=
XM_011534606.1:c.*4156A=	XP_011532908.1:n.*4156A=
XM_011534607.1:c.*4156A=	XP_011532909.1:n.*4156A=
XM_011534608.1:c.*4340A=	XP_011532910.1:n.*4340A=
XM_017009672.1:c.*4340A=	XP_016865161.1:n.*4340A=
XR_001742163.1:n.6041A=
XR_001742164.1:n.6026A=
NM_001303241.2:c.*4156A=	NP_001290170.1:n.*4156A=
NM_001370472.1:c.*4156A= MANE Select	NP_001357401.1:n.*4156A=
NM_001370473.1:c.*4156A=	NP_001357402.1:n.*4156A=
NM_001370474.1:c.*4156A=	NP_001357403.1:n.*4156A=
NR_163437.1:n.6321A=
NR_163438.1:n.6062A=