Canonical Allele Identifier: CA16602954
Gene: CNOT9 HGNC NCBI

Linked Data

ClinVar Variation Id: 376525
ClinVar RCV Id: RCV000439915
dbSNP Id: rs1057519955

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218584682C>T , CM000664.2:g.218584682C>T GRCh38
NC_000002.11:g.219449405C>T , CM000664.1:g.219449405C>T GRCh37
NC_000002.10:g.219157649C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000273064.11:c.391C>T MANE Select ENSP00000273064.6:p.Pro131Ser
ENST00000273064.10:c.391C>T ENSP00000273064.6:p.Pro131Ser
ENST00000295701.9:c.391C>T ENSP00000295701.5:p.Pro131Ser
ENST00000542068.5:c.391C>T ENSP00000443687.1:p.Pro131Ser
ENST00000627282.2:c.391C>T ENSP00000486540.1:p.Pro131Ser
NM_001271634.1:c.391C>T NP_001258563.1:p.Pro131Ser
NM_001271635.1:c.391C>T NP_001258564.1:p.Pro131Ser
NM_005444.2:c.391C>T NP_005435.1:p.Pro131Ser
NR_073390.1:n.695+1596C>T
XM_011512138.1:c.232C>T XP_011510440.1:p.Pro78Ser
XM_011512138.3:c.232C>T XP_011510440.1:p.Pro78Ser
XM_017005248.1:c.229C>T XP_016860737.1:p.Pro77Ser
XM_017005249.2:c.232C>T XP_016860738.1:p.Pro78Ser
NM_001271634.2:c.391C>T NP_001258563.1:p.Pro131Ser
NM_005444.3:c.391C>T MANE Select NP_005435.1:p.Pro131Ser
NR_073390.2:n.436+1596C>T
NM_001271635.2:c.391C>T NP_001258564.1:p.Pro131Ser