Canonical Allele Identifier: CA431228396

Gene: CNOT9

Linked Data

• MyVariant Identifiers: chr2:g.219449350A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218584627A>T , CM000664.2:g.218584627A>T	GRCh38
NC_000002.11:g.219449350A>T , CM000664.1:g.219449350A>T	GRCh37
NC_000002.10:g.219157594A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273064.11:c.336A>T MANE Select	ENSP00000273064.6:p.Ala112=
ENST00000273064.10:c.336A>T	ENSP00000273064.6:p.Ala112=
ENST00000295701.9:c.336A>T	ENSP00000295701.5:p.Ala112=
ENST00000432877.5:c.*228A>T	ENSP00000392394.1:n.*228A>T
ENST00000542068.5:c.336A>T	ENSP00000443687.1:p.Ala112=
ENST00000627282.2:c.336A>T	ENSP00000486540.1:p.Ala112=
NM_001271634.1:c.336A>T	NP_001258563.1:p.Ala112=
NM_001271635.1:c.336A>T	NP_001258564.1:p.Ala112=
NM_005444.2:c.336A>T	NP_005435.1:p.Ala112=
NR_073390.1:n.695+1541A>T
XM_011512138.1:c.177A>T	XP_011510440.1:p.Ala59=
XM_011512138.3:c.177A>T	XP_011510440.1:p.Ala59=
XM_017005248.1:c.174A>T	XP_016860737.1:p.Ala58=
XM_017005249.2:c.177A>T	XP_016860738.1:p.Ala59=
NM_001271634.2:c.336A>T	NP_001258563.1:p.Ala112=
NM_005444.3:c.336A>T MANE Select	NP_005435.1:p.Ala112=
NR_073390.2:n.436+1541A>T
NM_001271635.2:c.336A>T	NP_001258564.1:p.Ala112=