Canonical Allele Identifier: CA2663138965

Gene: CNOT9

Linked Data

• gnomAD v4: 2-218584498-T-TTCCTTGCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584500_218584508dup , CM000664.2:g.218584500_218584508dup	GRCh38
NC_000002.11:g.219449223_219449231dup , CM000664.1:g.219449223_219449231dup	GRCh37
NC_000002.10:g.219157467_219157475dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.321-112_321-104dup MANE Select	ENSP00000273064.6:n.321-112_321-104dup
ENST00000273064.10:c.321-112_321-104dup	ENSP00000273064.6:n.321-112_321-104dup
ENST00000295701.9:c.321-112_321-104dup	ENSP00000295701.5:n.321-112_321-104dup
ENST00000432877.5:c.*213-112_*213-104dup	ENSP00000392394.1:n.*213-112_*213-104dup
ENST00000542068.5:c.321-112_321-104dup	ENSP00000443687.1:n.321-112_321-104dup
ENST00000627282.2:c.321-112_321-104dup	ENSP00000486540.1:n.321-112_321-104dup
NM_001271634.1:c.321-112_321-104dup	NP_001258563.1:n.321-112_321-104dup
NM_001271635.1:c.321-112_321-104dup	NP_001258564.1:n.321-112_321-104dup
NM_005444.2:c.321-112_321-104dup	NP_005435.1:n.321-112_321-104dup
NR_073390.1:n.695+1414_695+1422dup
XM_011512138.1:c.162-112_162-104dup	XP_011510440.1:n.162-112_162-104dup
XM_011512138.3:c.162-112_162-104dup	XP_011510440.1:n.162-112_162-104dup
XM_017005248.1:c.159-112_159-104dup	XP_016860737.1:n.159-112_159-104dup
XM_017005249.2:c.162-112_162-104dup	XP_016860738.1:n.162-112_162-104dup
NM_001271634.2:c.321-112_321-104dup	NP_001258563.1:n.321-112_321-104dup
NM_005444.3:c.321-112_321-104dup MANE Select	NP_005435.1:n.321-112_321-104dup
NR_073390.2:n.436+1414_436+1422dup
NM_001271635.2:c.321-112_321-104dup	NP_001258564.1:n.321-112_321-104dup