Canonical Allele Identifier: CA133213890

Gene: CNOT6

Linked Data

• dbSNP Id: rs921360473
• gnomAD v3: 5-180578301-C-T
• gnomAD v4: 5-180578301-C-T
• MyVariant Identifiers: chr5:g.180005301C>T (hg19) ; chr5:g.180578301C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180578301C>T , CM000667.2:g.180578301C>T	GRCh38
NC_000005.9:g.180005301C>T , CM000667.1:g.180005301C>T	GRCh37
NC_000005.8:g.179937907C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261951.9:c.*4101C>T MANE Select	ENSP00000261951.4:n.*4101C>T
ENST00000393356.7:c.*4101C>T	ENSP00000377024.1:n.*4101C>T
ENST00000261951.8:c.*4101C>T	ENSP00000261951.4:n.*4101C>T
ENST00000393356.5:c.*4101C>T	ENSP00000377024.1:n.*4101C>T
ENST00000618123.4:c.*4101C>T	ENSP00000481893.1:n.*4101C>T
NM_001303241.1:c.*4101C>T	NP_001290170.1:n.*4101C>T
XM_005265953.1:c.*4101C>T	XP_005266010.1:n.*4101C>T
XM_011534605.1:c.*4101C>T	XP_011532907.1:n.*4101C>T
XM_011534606.1:c.*4101C>T	XP_011532908.1:n.*4101C>T
XM_011534607.1:c.*4101C>T	XP_011532909.1:n.*4101C>T
XM_011534608.1:c.*4285C>T	XP_011532910.1:n.*4285C>T
XM_017009672.1:c.*4285C>T	XP_016865161.1:n.*4285C>T
XR_001742163.1:n.5986C>T
XR_001742164.1:n.5971C>T
NM_001303241.2:c.*4101C>T	NP_001290170.1:n.*4101C>T
NM_001370472.1:c.*4101C>T MANE Select	NP_001357401.1:n.*4101C>T
NM_001370473.1:c.*4101C>T	NP_001357402.1:n.*4101C>T
NM_001370474.1:c.*4101C>T	NP_001357403.1:n.*4101C>T
NR_163437.1:n.6266C>T
NR_163438.1:n.6007C>T