Canonical Allele Identifier: CA1864666394
Gene: FAM120AOS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93447641T= , CM000671.2:g.93447641T= GRCh38
NC_000009.11:g.96209923T= , CM000671.1:g.96209923T= GRCh37
NC_000009.10:g.95249744T= NCBI36
NG_054727.1:g.10961A=

Transcript Alleles

HGVS Amino-acid change
ENST00000375412.11:c.741A= MANE Select ENSP00000364561.5:p.Pro247=
ENST00000649557.1:c.195A= ENSP00000496904.1:p.Pro65=
ENST00000650398.1:n.764A=
ENST00000375412.9:c.741A= ENSP00000364561.5:p.Pro247=
ENST00000423591.5:c.195A= ENSP00000414298.1:p.Pro65=
ENST00000428152.1:n.457A=
ENST00000428378.1:c.192A= ENSP00000416978.1:p.Pro64=
ENST00000476484.5:c.*139A= ENSP00000429212.1:n.*139A=
ENST00000479094.5:n.758A=
ENST00000483056.5:n.563A=
ENST00000483149.6:n.696A=
ENST00000520403.1:n.738A=
ENST00000520470.5:n.817A=
ENST00000523407.1:n.619A=
NM_198841.2:c.741A= NP_942138.2:p.Pro247=
XM_005251736.2:c.828A= XP_005251793.1:p.Pro276=
NM_001322224.2:c.195A= NP_001309153.1:p.Pro65=
NM_198841.3:c.741A= NP_942138.2:p.Pro247=
NR_136229.2:n.1040A=
NR_136230.2:n.1161A=
NR_136231.2:n.1754A=
NR_136232.2:n.966A=
NR_136233.2:n.789A=
NR_136234.2:n.823A=
NR_136235.2:n.845A=
NR_136236.2:n.1048A=
NR_136237.2:n.1169A=
NR_136238.2:n.910A=
NM_198841.4:c.741A= MANE Select NP_942138.2:p.Pro247=
NM_001322224.3:c.195A= NP_001309153.1:p.Pro65=
NR_136231.3:n.1734A=
NR_136232.3:n.963A=
NR_136233.3:n.786A=
NR_136234.3:n.820A=
NR_136235.3:n.842A=
NR_136236.3:n.1045A=
NR_136237.3:n.1166A=
NR_136238.3:n.907A=