Canonical Allele Identifier: CA65779093

Gene: CNOT9

Linked Data

• dbSNP Id: rs955783199
• gnomAD v3: 2-218584598-T-C
• gnomAD v4: 2-218584598-T-C
• MyVariant Identifiers: chr2:g.219449321T>C (hg19) ; chr2:g.218584598T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584598T>C , CM000664.2:g.218584598T>C	GRCh38
NC_000002.11:g.219449321T>C , CM000664.1:g.219449321T>C	GRCh37
NC_000002.10:g.219157565T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000273064.11:c.321-14T>C MANE Select	ENSP00000273064.6:n.321-14T>C
ENST00000273064.10:c.321-14T>C	ENSP00000273064.6:n.321-14T>C
ENST00000295701.9:c.321-14T>C	ENSP00000295701.5:n.321-14T>C
ENST00000432877.5:c.*213-14T>C	ENSP00000392394.1:n.*213-14T>C
ENST00000542068.5:c.321-14T>C	ENSP00000443687.1:n.321-14T>C
ENST00000627282.2:c.321-14T>C	ENSP00000486540.1:n.321-14T>C
NM_001271634.1:c.321-14T>C	NP_001258563.1:n.321-14T>C
NM_001271635.1:c.321-14T>C	NP_001258564.1:n.321-14T>C
NM_005444.2:c.321-14T>C	NP_005435.1:n.321-14T>C
NR_073390.1:n.695+1512T>C
XM_011512138.1:c.162-14T>C	XP_011510440.1:n.162-14T>C
XM_011512138.3:c.162-14T>C	XP_011510440.1:n.162-14T>C
XM_017005248.1:c.159-14T>C	XP_016860737.1:n.159-14T>C
XM_017005249.2:c.162-14T>C	XP_016860738.1:n.162-14T>C
NM_001271634.2:c.321-14T>C	NP_001258563.1:n.321-14T>C
NM_005444.3:c.321-14T>C MANE Select	NP_005435.1:n.321-14T>C
NR_073390.2:n.436+1512T>C
NM_001271635.2:c.321-14T>C	NP_001258564.1:n.321-14T>C