Canonical Allele Identifier: CA2568238791

Gene: CNOT9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584582_218584583insGA , CM000664.2:g.218584582_218584583insGA	GRCh38
NC_000002.11:g.219449305_219449306insGA , CM000664.1:g.219449305_219449306insGA	GRCh37
NC_000002.10:g.219157549_219157550insGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.321-30_321-29insGA MANE Select	ENSP00000273064.6:n.321-30_321-29insGA
ENST00000273064.10:c.321-30_321-29insGA	ENSP00000273064.6:n.321-30_321-29insGA
ENST00000295701.9:c.321-30_321-29insGA	ENSP00000295701.5:n.321-30_321-29insGA
ENST00000432877.5:c.*213-30_*213-29insGA	ENSP00000392394.1:n.*213-30_*213-29insGA
ENST00000542068.5:c.321-30_321-29insGA	ENSP00000443687.1:n.321-30_321-29insGA
ENST00000627282.2:c.321-30_321-29insGA	ENSP00000486540.1:n.321-30_321-29insGA
NM_001271634.1:c.321-30_321-29insGA	NP_001258563.1:n.321-30_321-29insGA
NM_001271635.1:c.321-30_321-29insGA	NP_001258564.1:n.321-30_321-29insGA
NM_005444.2:c.321-30_321-29insGA	NP_005435.1:n.321-30_321-29insGA
NR_073390.1:n.695+1496_695+1497insGA
XM_011512138.1:c.162-30_162-29insGA	XP_011510440.1:n.162-30_162-29insGA
XM_011512138.3:c.162-30_162-29insGA	XP_011510440.1:n.162-30_162-29insGA
XM_017005248.1:c.159-30_159-29insGA	XP_016860737.1:n.159-30_159-29insGA
XM_017005249.2:c.162-30_162-29insGA	XP_016860738.1:n.162-30_162-29insGA
NM_001271634.2:c.321-30_321-29insGA	NP_001258563.1:n.321-30_321-29insGA
NM_005444.3:c.321-30_321-29insGA MANE Select	NP_005435.1:n.321-30_321-29insGA
NR_073390.2:n.436+1496_436+1497insGA
NM_001271635.2:c.321-30_321-29insGA	NP_001258564.1:n.321-30_321-29insGA