Canonical Allele Identifier: CA1864666285

Gene: FAM120AOS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.93447552T= , CM000671.2:g.93447552T=	GRCh38
NC_000009.11:g.96209834T= , CM000671.1:g.96209834T=	GRCh37
NC_000009.10:g.95249655T=	NCBI36
NG_054727.1:g.11050A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375412.11:c.*59A= MANE Select	ENSP00000364561.5:n.*59A=
ENST00000649557.1:c.*59A=	ENSP00000496904.1:n.*59A=
ENST00000650398.1:n.853A=
ENST00000375412.9:c.*59A=	ENSP00000364561.5:n.*59A=
ENST00000423591.5:c.*59A=	ENSP00000414298.1:n.*59A=
ENST00000428152.1:n.546A=
ENST00000476484.5:c.*228A=	ENSP00000429212.1:n.*228A=
ENST00000479094.5:n.847A=
ENST00000483056.5:n.652A=
ENST00000483149.6:n.785A=
ENST00000520403.1:n.827A=
ENST00000520470.5:n.906A=
ENST00000523407.1:n.708A=
NM_198841.2:c.*59A=	NP_942138.2:n.*59A=
XM_005251736.2:c.917A=	XP_005251793.1:n.917A=
NM_001322224.2:c.*59A=	NP_001309153.1:n.*59A=
NM_198841.3:c.*59A=	NP_942138.2:n.*59A=
NR_136229.2:n.1129A=
NR_136230.2:n.1250A=
NR_136231.2:n.1843A=
NR_136232.2:n.1055A=
NR_136233.2:n.878A=
NR_136234.2:n.912A=
NR_136235.2:n.934A=
NR_136236.2:n.1137A=
NR_136237.2:n.1258A=
NR_136238.2:n.999A=
NM_198841.4:c.*59A= MANE Select	NP_942138.2:n.*59A=
NM_001322224.3:c.*59A=	NP_001309153.1:n.*59A=
NR_136231.3:n.1823A=
NR_136232.3:n.1052A=
NR_136233.3:n.875A=
NR_136234.3:n.909A=
NR_136235.3:n.931A=
NR_136236.3:n.1134A=
NR_136237.3:n.1255A=
NR_136238.3:n.996A=