Canonical Allele Identifier: CA1864666287

Gene: FAM120AOS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.93447554G= , CM000671.2:g.93447554G=	GRCh38
NC_000009.11:g.96209836G= , CM000671.1:g.96209836G=	GRCh37
NC_000009.10:g.95249657G=	NCBI36
NG_054727.1:g.11048C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375412.11:c.*57C= MANE Select	ENSP00000364561.5:n.*57C=
ENST00000649557.1:c.*57C=	ENSP00000496904.1:n.*57C=
ENST00000650398.1:n.851C=
ENST00000375412.9:c.*57C=	ENSP00000364561.5:n.*57C=
ENST00000423591.5:c.*57C=	ENSP00000414298.1:n.*57C=
ENST00000428152.1:n.544C=
ENST00000476484.5:c.*226C=	ENSP00000429212.1:n.*226C=
ENST00000479094.5:n.845C=
ENST00000483056.5:n.650C=
ENST00000483149.6:n.783C=
ENST00000520403.1:n.825C=
ENST00000520470.5:n.904C=
ENST00000523407.1:n.706C=
NM_198841.2:c.*57C=	NP_942138.2:n.*57C=
XM_005251736.2:c.915C=	XP_005251793.1:n.915C=
NM_001322224.2:c.*57C=	NP_001309153.1:n.*57C=
NM_198841.3:c.*57C=	NP_942138.2:n.*57C=
NR_136229.2:n.1127C=
NR_136230.2:n.1248C=
NR_136231.2:n.1841C=
NR_136232.2:n.1053C=
NR_136233.2:n.876C=
NR_136234.2:n.910C=
NR_136235.2:n.932C=
NR_136236.2:n.1135C=
NR_136237.2:n.1256C=
NR_136238.2:n.997C=
NM_198841.4:c.*57C= MANE Select	NP_942138.2:n.*57C=
NM_001322224.3:c.*57C=	NP_001309153.1:n.*57C=
NR_136231.3:n.1821C=
NR_136232.3:n.1050C=
NR_136233.3:n.873C=
NR_136234.3:n.907C=
NR_136235.3:n.929C=
NR_136236.3:n.1132C=
NR_136237.3:n.1253C=
NR_136238.3:n.994C=