Canonical Allele Identifier: CA466069698

Gene: FAM120AOS

Linked Data

• MyVariant Identifiers: chr9:g.96209932T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.93447650T>A , CM000671.2:g.93447650T>A	GRCh38
NC_000009.11:g.96209932T>A , CM000671.1:g.96209932T>A	GRCh37
NC_000009.10:g.95249753T>A	NCBI36
NG_054727.1:g.10952A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375412.11:c.732A>T MANE Select	ENSP00000364561.5:p.Thr244=
ENST00000649557.1:c.186A>T	ENSP00000496904.1:p.Thr62=
ENST00000650398.1:n.755A>T
ENST00000375412.9:c.732A>T	ENSP00000364561.5:p.Thr244=
ENST00000423591.5:c.186A>T	ENSP00000414298.1:p.Thr62=
ENST00000428152.1:n.448A>T
ENST00000428378.1:c.183A>T	ENSP00000416978.1:p.Thr61=
ENST00000476484.5:c.*130A>T	ENSP00000429212.1:n.*130A>T
ENST00000479094.5:n.749A>T
ENST00000483056.5:n.554A>T
ENST00000483149.6:n.687A>T
ENST00000520403.1:n.729A>T
ENST00000520470.5:n.808A>T
ENST00000523407.1:n.610A>T
NM_198841.2:c.732A>T	NP_942138.2:p.Thr244=
XM_005251736.2:c.819A>T	XP_005251793.1:p.Thr273=
NM_001322224.2:c.186A>T	NP_001309153.1:p.Thr62=
NM_198841.3:c.732A>T	NP_942138.2:p.Thr244=
NR_136229.2:n.1031A>T
NR_136230.2:n.1152A>T
NR_136231.2:n.1745A>T
NR_136232.2:n.957A>T
NR_136233.2:n.780A>T
NR_136234.2:n.814A>T
NR_136235.2:n.836A>T
NR_136236.2:n.1039A>T
NR_136237.2:n.1160A>T
NR_136238.2:n.901A>T
NM_198841.4:c.732A>T MANE Select	NP_942138.2:p.Thr244=
NM_001322224.3:c.186A>T	NP_001309153.1:p.Thr62=
NR_136231.3:n.1725A>T
NR_136232.3:n.954A>T
NR_136233.3:n.777A>T
NR_136234.3:n.811A>T
NR_136235.3:n.833A>T
NR_136236.3:n.1036A>T
NR_136237.3:n.1157A>T
NR_136238.3:n.898A>T