Canonical Allele Identifier: CA1864666401
Gene: FAM120AOS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93447646G= , CM000671.2:g.93447646G= GRCh38
NC_000009.11:g.96209928G= , CM000671.1:g.96209928G= GRCh37
NC_000009.10:g.95249749G= NCBI36
NG_054727.1:g.10956C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375412.11:c.736C= MANE Select ENSP00000364561.5:p.Pro246=
ENST00000649557.1:c.190C= ENSP00000496904.1:p.Pro64=
ENST00000650398.1:n.759C=
ENST00000375412.9:c.736C= ENSP00000364561.5:p.Pro246=
ENST00000423591.5:c.190C= ENSP00000414298.1:p.Pro64=
ENST00000428152.1:n.452C=
ENST00000428378.1:c.187C= ENSP00000416978.1:p.Pro63=
ENST00000476484.5:c.*134C= ENSP00000429212.1:n.*134C=
ENST00000479094.5:n.753C=
ENST00000483056.5:n.558C=
ENST00000483149.6:n.691C=
ENST00000520403.1:n.733C=
ENST00000520470.5:n.812C=
ENST00000523407.1:n.614C=
NM_198841.2:c.736C= NP_942138.2:p.Pro246=
XM_005251736.2:c.823C= XP_005251793.1:p.Pro275=
NM_001322224.2:c.190C= NP_001309153.1:p.Pro64=
NM_198841.3:c.736C= NP_942138.2:p.Pro246=
NR_136229.2:n.1035C=
NR_136230.2:n.1156C=
NR_136231.2:n.1749C=
NR_136232.2:n.961C=
NR_136233.2:n.784C=
NR_136234.2:n.818C=
NR_136235.2:n.840C=
NR_136236.2:n.1043C=
NR_136237.2:n.1164C=
NR_136238.2:n.905C=
NM_198841.4:c.736C= MANE Select NP_942138.2:p.Pro246=
NM_001322224.3:c.190C= NP_001309153.1:p.Pro64=
NR_136231.3:n.1729C=
NR_136232.3:n.958C=
NR_136233.3:n.781C=
NR_136234.3:n.815C=
NR_136235.3:n.837C=
NR_136236.3:n.1040C=
NR_136237.3:n.1161C=
NR_136238.3:n.902C=