Canonical Allele Identifier: CA1864666294

Gene: FAM120AOS

Linked Data

• dbSNP Id: rs1856895330

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.93447559dup , CM000671.2:g.93447559dup	GRCh38
NC_000009.11:g.96209841dup , CM000671.1:g.96209841dup	GRCh37
NC_000009.10:g.95249662dup	NCBI36
NG_054727.1:g.11043dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375412.11:c.*52dup MANE Select	ENSP00000364561.5:n.*52dup
ENST00000649557.1:c.*52dup	ENSP00000496904.1:n.*52dup
ENST00000650398.1:n.846dup
ENST00000375412.9:c.*52dup	ENSP00000364561.5:n.*52dup
ENST00000423591.5:c.*52dup	ENSP00000414298.1:n.*52dup
ENST00000428152.1:n.539dup
ENST00000476484.5:c.*221dup	ENSP00000429212.1:n.*221dup
ENST00000479094.5:n.840dup
ENST00000483056.5:n.645dup
ENST00000483149.6:n.778dup
ENST00000520403.1:n.820dup
ENST00000520470.5:n.899dup
ENST00000523407.1:n.701dup
NM_198841.2:c.*52dup	NP_942138.2:n.*52dup
XM_005251736.2:c.910dup	XP_005251793.1:n.910dup
NM_001322224.2:c.*52dup	NP_001309153.1:n.*52dup
NM_198841.3:c.*52dup	NP_942138.2:n.*52dup
NR_136229.2:n.1122dup
NR_136230.2:n.1243dup
NR_136231.2:n.1836dup
NR_136232.2:n.1048dup
NR_136233.2:n.871dup
NR_136234.2:n.905dup
NR_136235.2:n.927dup
NR_136236.2:n.1130dup
NR_136237.2:n.1251dup
NR_136238.2:n.992dup
NM_198841.4:c.*52dup MANE Select	NP_942138.2:n.*52dup
NM_001322224.3:c.*52dup	NP_001309153.1:n.*52dup
NR_136231.3:n.1816dup
NR_136232.3:n.1045dup
NR_136233.3:n.868dup
NR_136234.3:n.902dup
NR_136235.3:n.924dup
NR_136236.3:n.1127dup
NR_136237.3:n.1248dup
NR_136238.3:n.989dup