Canonical Allele Identifier: CA764891534

Gene: CNOT9

Linked Data

• dbSNP Id: rs1227932574
• gnomAD v4: 2-218582953-C-T
• MyVariant Identifiers: chr2:g.219447676C>T (hg19) ; chr2:g.218582953C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218582953C>T , CM000664.2:g.218582953C>T	GRCh38
NC_000002.11:g.219447676C>T , CM000664.1:g.219447676C>T	GRCh37
NC_000002.10:g.219155920C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.205-18C>T MANE Select	ENSP00000273064.6:n.205-18C>T
ENST00000273064.10:c.205-18C>T	ENSP00000273064.6:n.205-18C>T
ENST00000295701.9:c.205-18C>T	ENSP00000295701.5:n.205-18C>T
ENST00000432877.5:c.*97-18C>T	ENSP00000392394.1:n.*97-18C>T
ENST00000542068.5:c.205-18C>T	ENSP00000443687.1:n.205-18C>T
ENST00000627282.2:c.205-18C>T	ENSP00000486540.1:n.205-18C>T
NM_001271634.1:c.205-18C>T	NP_001258563.1:n.205-18C>T
NM_001271635.1:c.205-18C>T	NP_001258564.1:n.205-18C>T
NM_005444.2:c.205-18C>T	NP_005435.1:n.205-18C>T
NR_073390.1:n.580-18C>T
XM_011512138.1:c.46-18C>T	XP_011510440.1:n.46-18C>T
XM_011512138.3:c.46-18C>T	XP_011510440.1:n.46-18C>T
XM_017005248.1:c.43-18C>T	XP_016860737.1:n.43-18C>T
XM_017005249.2:c.46-18C>T	XP_016860738.1:n.46-18C>T
NM_001271634.2:c.205-18C>T	NP_001258563.1:n.205-18C>T
NM_005444.3:c.205-18C>T MANE Select	NP_005435.1:n.205-18C>T
NR_073390.2:n.321-18C>T
NM_001271635.2:c.205-18C>T	NP_001258564.1:n.205-18C>T