Canonical Allele Identifier: CA539604736

Gene: CNOT9

Linked Data

• dbSNP Id: rs1265530872
• gnomAD v2: 2-219447827-G-GA
• gnomAD v3: 2-218583104-G-GA
• gnomAD v4: 2-218583104-G-GA
• MyVariant Identifiers: chr2:g.219447827_219447828insA (hg19) ; chr2:g.218583104_218583105insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218583104_218583105insA , CM000664.2:g.218583104_218583105insA	GRCh38
NC_000002.11:g.219447827_219447828insA , CM000664.1:g.219447827_219447828insA	GRCh37
NC_000002.10:g.219156071_219156072insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.320+18_320+19insA MANE Select	ENSP00000273064.6:n.320+18_320+19insA
ENST00000273064.10:c.320+18_320+19insA	ENSP00000273064.6:n.320+18_320+19insA
ENST00000295701.9:c.320+18_320+19insA	ENSP00000295701.5:n.320+18_320+19insA
ENST00000432877.5:c.*212+18_*212+19insA	ENSP00000392394.1:n.*212+18_*212+19insA
ENST00000542068.5:c.320+18_320+19insA	ENSP00000443687.1:n.320+18_320+19insA
ENST00000627282.2:c.320+18_320+19insA	ENSP00000486540.1:n.320+18_320+19insA
NM_001271634.1:c.320+18_320+19insA	NP_001258563.1:n.320+18_320+19insA
NM_001271635.1:c.320+18_320+19insA	NP_001258564.1:n.320+18_320+19insA
NM_005444.2:c.320+18_320+19insA	NP_005435.1:n.320+18_320+19insA
NR_073390.1:n.695+18_695+19insA
XM_011512138.1:c.161+18_161+19insA	XP_011510440.1:n.161+18_161+19insA
XM_011512138.3:c.161+18_161+19insA	XP_011510440.1:n.161+18_161+19insA
XM_017005248.1:c.158+18_158+19insA	XP_016860737.1:n.158+18_158+19insA
XM_017005249.2:c.161+18_161+19insA	XP_016860738.1:n.161+18_161+19insA
NM_001271634.2:c.320+18_320+19insA	NP_001258563.1:n.320+18_320+19insA
NM_005444.3:c.320+18_320+19insA MANE Select	NP_005435.1:n.320+18_320+19insA
NR_073390.2:n.436+18_436+19insA
NM_001271635.2:c.320+18_320+19insA	NP_001258564.1:n.320+18_320+19insA