Canonical Allele Identifier: CA374064339

Gene: FAM120AOS

Linked Data

• MyVariant Identifiers: chr9:g.96209925G>T (hg19) ; chr9:g.93447643G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.93447643G>T , CM000671.2:g.93447643G>T	GRCh38
NC_000009.11:g.96209925G>T , CM000671.1:g.96209925G>T	GRCh37
NC_000009.10:g.95249746G>T	NCBI36
NG_054727.1:g.10959C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375412.11:c.739C>A MANE Select	ENSP00000364561.5:p.Pro247Thr
ENST00000649557.1:c.193C>A	ENSP00000496904.1:p.Pro65Thr
ENST00000650398.1:n.762C>A
ENST00000375412.9:c.739C>A	ENSP00000364561.5:p.Pro247Thr
ENST00000423591.5:c.193C>A	ENSP00000414298.1:p.Pro65Thr
ENST00000428152.1:n.455C>A
ENST00000428378.1:c.190C>A	ENSP00000416978.1:p.Pro64Thr
ENST00000476484.5:c.*137C>A	ENSP00000429212.1:n.*137C>A
ENST00000479094.5:n.756C>A
ENST00000483056.5:n.561C>A
ENST00000483149.6:n.694C>A
ENST00000520403.1:n.736C>A
ENST00000520470.5:n.815C>A
ENST00000523407.1:n.617C>A
NM_198841.2:c.739C>A	NP_942138.2:p.Pro247Thr
XM_005251736.2:c.826C>A	XP_005251793.1:p.Pro276Thr
NM_001322224.2:c.193C>A	NP_001309153.1:p.Pro65Thr
NM_198841.3:c.739C>A	NP_942138.2:p.Pro247Thr
NR_136229.2:n.1038C>A
NR_136230.2:n.1159C>A
NR_136231.2:n.1752C>A
NR_136232.2:n.964C>A
NR_136233.2:n.787C>A
NR_136234.2:n.821C>A
NR_136235.2:n.843C>A
NR_136236.2:n.1046C>A
NR_136237.2:n.1167C>A
NR_136238.2:n.908C>A
NM_198841.4:c.739C>A MANE Select	NP_942138.2:p.Pro247Thr
NM_001322224.3:c.193C>A	NP_001309153.1:p.Pro65Thr
NR_136231.3:n.1732C>A
NR_136232.3:n.961C>A
NR_136233.3:n.784C>A
NR_136234.3:n.818C>A
NR_136235.3:n.840C>A
NR_136236.3:n.1043C>A
NR_136237.3:n.1164C>A
NR_136238.3:n.905C>A