Canonical Allele Identifier: CA1864666387
Gene: FAM120AOS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93447639G= , CM000671.2:g.93447639G= GRCh38
NC_000009.11:g.96209921G= , CM000671.1:g.96209921G= GRCh37
NC_000009.10:g.95249742G= NCBI36
NG_054727.1:g.10963C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375412.11:c.743C= MANE Select ENSP00000364561.5:p.Thr248=
ENST00000649557.1:c.197C= ENSP00000496904.1:p.Thr66=
ENST00000650398.1:n.766C=
ENST00000375412.9:c.743C= ENSP00000364561.5:p.Thr248=
ENST00000423591.5:c.197C= ENSP00000414298.1:p.Thr66=
ENST00000428152.1:n.459C=
ENST00000428378.1:c.194C= ENSP00000416978.1:p.Thr65=
ENST00000476484.5:c.*141C= ENSP00000429212.1:n.*141C=
ENST00000479094.5:n.760C=
ENST00000483056.5:n.565C=
ENST00000483149.6:n.698C=
ENST00000520403.1:n.740C=
ENST00000520470.5:n.819C=
ENST00000523407.1:n.621C=
NM_198841.2:c.743C= NP_942138.2:p.Thr248=
XM_005251736.2:c.830C= XP_005251793.1:p.Thr277=
NM_001322224.2:c.197C= NP_001309153.1:p.Thr66=
NM_198841.3:c.743C= NP_942138.2:p.Thr248=
NR_136229.2:n.1042C=
NR_136230.2:n.1163C=
NR_136231.2:n.1756C=
NR_136232.2:n.968C=
NR_136233.2:n.791C=
NR_136234.2:n.825C=
NR_136235.2:n.847C=
NR_136236.2:n.1050C=
NR_136237.2:n.1171C=
NR_136238.2:n.912C=
NM_198841.4:c.743C= MANE Select NP_942138.2:p.Thr248=
NM_001322224.3:c.197C= NP_001309153.1:p.Thr66=
NR_136231.3:n.1736C=
NR_136232.3:n.965C=
NR_136233.3:n.788C=
NR_136234.3:n.822C=
NR_136235.3:n.844C=
NR_136236.3:n.1047C=
NR_136237.3:n.1168C=
NR_136238.3:n.909C=