Canonical Allele Identifier: CA350569176
Gene: CNOT9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218584697C>G , CM000664.2:g.218584697C>G GRCh38
NC_000002.11:g.219449420C>G , CM000664.1:g.219449420C>G GRCh37
NC_000002.10:g.219157664C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000273064.11:c.406C>G MANE Select ENSP00000273064.6:p.Arg136Gly
ENST00000273064.10:c.406C>G ENSP00000273064.6:p.Arg136Gly
ENST00000295701.9:c.406C>G ENSP00000295701.5:p.Arg136Gly
ENST00000542068.5:c.406C>G ENSP00000443687.1:p.Arg136Gly
ENST00000627282.2:c.406C>G ENSP00000486540.1:p.Arg136Gly
NM_001271634.1:c.406C>G NP_001258563.1:p.Arg136Gly
NM_001271635.1:c.406C>G NP_001258564.1:p.Arg136Gly
NM_005444.2:c.406C>G NP_005435.1:p.Arg136Gly
NR_073390.1:n.695+1611C>G
XM_011512138.1:c.247C>G XP_011510440.1:p.Arg83Gly
XM_011512138.3:c.247C>G XP_011510440.1:p.Arg83Gly
XM_017005248.1:c.244C>G XP_016860737.1:p.Arg82Gly
XM_017005249.2:c.247C>G XP_016860738.1:p.Arg83Gly
NM_001271634.2:c.406C>G NP_001258563.1:p.Arg136Gly
NM_005444.3:c.406C>G MANE Select NP_005435.1:p.Arg136Gly
NR_073390.2:n.436+1611C>G
NM_001271635.2:c.406C>G NP_001258564.1:p.Arg136Gly