Canonical Allele Identifier: CA1864666404
Gene: FAM120AOS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93447648T= , CM000671.2:g.93447648T= GRCh38
NC_000009.11:g.96209930T= , CM000671.1:g.96209930T= GRCh37
NC_000009.10:g.95249751T= NCBI36
NG_054727.1:g.10954A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375412.11:c.734A= MANE Select ENSP00000364561.5:p.Lys245=
ENST00000649557.1:c.188A= ENSP00000496904.1:p.Lys63=
ENST00000650398.1:n.757A=
ENST00000375412.9:c.734A= ENSP00000364561.5:p.Lys245=
ENST00000423591.5:c.188A= ENSP00000414298.1:p.Lys63=
ENST00000428152.1:n.450A=
ENST00000428378.1:c.185A= ENSP00000416978.1:p.Lys62=
ENST00000476484.5:c.*132A= ENSP00000429212.1:n.*132A=
ENST00000479094.5:n.751A=
ENST00000483056.5:n.556A=
ENST00000483149.6:n.689A=
ENST00000520403.1:n.731A=
ENST00000520470.5:n.810A=
ENST00000523407.1:n.612A=
NM_198841.2:c.734A= NP_942138.2:p.Lys245=
XM_005251736.2:c.821A= XP_005251793.1:p.Lys274=
NM_001322224.2:c.188A= NP_001309153.1:p.Lys63=
NM_198841.3:c.734A= NP_942138.2:p.Lys245=
NR_136229.2:n.1033A=
NR_136230.2:n.1154A=
NR_136231.2:n.1747A=
NR_136232.2:n.959A=
NR_136233.2:n.782A=
NR_136234.2:n.816A=
NR_136235.2:n.838A=
NR_136236.2:n.1041A=
NR_136237.2:n.1162A=
NR_136238.2:n.903A=
NM_198841.4:c.734A= MANE Select NP_942138.2:p.Lys245=
NM_001322224.3:c.188A= NP_001309153.1:p.Lys63=
NR_136231.3:n.1727A=
NR_136232.3:n.956A=
NR_136233.3:n.779A=
NR_136234.3:n.813A=
NR_136235.3:n.835A=
NR_136236.3:n.1038A=
NR_136237.3:n.1159A=
NR_136238.3:n.900A=