Canonical Allele Identifier: CA1864666297

Gene: FAM120AOS

Linked Data

• dbSNP Id: rs1856895162
• gnomAD v4: 9-93447559-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.93447559C>T , CM000671.2:g.93447559C>T	GRCh38
NC_000009.11:g.96209841C>T , CM000671.1:g.96209841C>T	GRCh37
NC_000009.10:g.95249662C>T	NCBI36
NG_054727.1:g.11043G>A

Transcript Alleles

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