Canonical Allele Identifier: CA466069696

Gene: FAM120AOS

Linked Data

• MyVariant Identifiers: chr9:g.96209926T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.93447644T>G , CM000671.2:g.93447644T>G	GRCh38
NC_000009.11:g.96209926T>G , CM000671.1:g.96209926T>G	GRCh37
NC_000009.10:g.95249747T>G	NCBI36
NG_054727.1:g.10958A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375412.11:c.738A>C MANE Select	ENSP00000364561.5:p.Pro246=
ENST00000649557.1:c.192A>C	ENSP00000496904.1:p.Pro64=
ENST00000650398.1:n.761A>C
ENST00000375412.9:c.738A>C	ENSP00000364561.5:p.Pro246=
ENST00000423591.5:c.192A>C	ENSP00000414298.1:p.Pro64=
ENST00000428152.1:n.454A>C
ENST00000428378.1:c.189A>C	ENSP00000416978.1:p.Pro63=
ENST00000476484.5:c.*136A>C	ENSP00000429212.1:n.*136A>C
ENST00000479094.5:n.755A>C
ENST00000483056.5:n.560A>C
ENST00000483149.6:n.693A>C
ENST00000520403.1:n.735A>C
ENST00000520470.5:n.814A>C
ENST00000523407.1:n.616A>C
NM_198841.2:c.738A>C	NP_942138.2:p.Pro246=
XM_005251736.2:c.825A>C	XP_005251793.1:p.Pro275=
NM_001322224.2:c.192A>C	NP_001309153.1:p.Pro64=
NM_198841.3:c.738A>C	NP_942138.2:p.Pro246=
NR_136229.2:n.1037A>C
NR_136230.2:n.1158A>C
NR_136231.2:n.1751A>C
NR_136232.2:n.963A>C
NR_136233.2:n.786A>C
NR_136234.2:n.820A>C
NR_136235.2:n.842A>C
NR_136236.2:n.1045A>C
NR_136237.2:n.1166A>C
NR_136238.2:n.907A>C
NM_198841.4:c.738A>C MANE Select	NP_942138.2:p.Pro246=
NM_001322224.3:c.192A>C	NP_001309153.1:p.Pro64=
NR_136231.3:n.1731A>C
NR_136232.3:n.960A>C
NR_136233.3:n.783A>C
NR_136234.3:n.817A>C
NR_136235.3:n.839A>C
NR_136236.3:n.1042A>C
NR_136237.3:n.1163A>C
NR_136238.3:n.904A>C