Canonical Allele Identifier: CA350569020
Gene: CNOT9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218584628G>C , CM000664.2:g.218584628G>C GRCh38
NC_000002.11:g.219449351G>C , CM000664.1:g.219449351G>C GRCh37
NC_000002.10:g.219157595G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000273064.11:c.337G>C MANE Select ENSP00000273064.6:p.Ala113Pro
ENST00000273064.10:c.337G>C ENSP00000273064.6:p.Ala113Pro
ENST00000295701.9:c.337G>C ENSP00000295701.5:p.Ala113Pro
ENST00000432877.5:c.*229G>C ENSP00000392394.1:n.*229G>C
ENST00000542068.5:c.337G>C ENSP00000443687.1:p.Ala113Pro
ENST00000627282.2:c.337G>C ENSP00000486540.1:p.Ala113Pro
NM_001271634.1:c.337G>C NP_001258563.1:p.Ala113Pro
NM_001271635.1:c.337G>C NP_001258564.1:p.Ala113Pro
NM_005444.2:c.337G>C NP_005435.1:p.Ala113Pro
NR_073390.1:n.695+1542G>C
XM_011512138.1:c.178G>C XP_011510440.1:p.Ala60Pro
XM_011512138.3:c.178G>C XP_011510440.1:p.Ala60Pro
XM_017005248.1:c.175G>C XP_016860737.1:p.Ala59Pro
XM_017005249.2:c.178G>C XP_016860738.1:p.Ala60Pro
NM_001271634.2:c.337G>C NP_001258563.1:p.Ala113Pro
NM_005444.3:c.337G>C MANE Select NP_005435.1:p.Ala113Pro
NR_073390.2:n.436+1542G>C
NM_001271635.2:c.337G>C NP_001258564.1:p.Ala113Pro