Canonical Allele Identifier: CA2580884376

Gene: FAM120AOS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.93447550G>C , CM000671.2:g.93447550G>C	GRCh38
NC_000009.11:g.96209832G>C , CM000671.1:g.96209832G>C	GRCh37
NC_000009.10:g.95249653G>C	NCBI36
NG_054727.1:g.11052C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375412.11:c.*61C>G MANE Select	ENSP00000364561.5:n.*61C>G
ENST00000649557.1:c.*61C>G	ENSP00000496904.1:n.*61C>G
ENST00000650398.1:n.855C>G
ENST00000375412.9:c.*61C>G	ENSP00000364561.5:n.*61C>G
ENST00000423591.5:c.*61C>G	ENSP00000414298.1:n.*61C>G
ENST00000428152.1:n.548C>G
ENST00000476484.5:c.*230C>G	ENSP00000429212.1:n.*230C>G
ENST00000479094.5:n.849C>G
ENST00000483056.5:n.654C>G
ENST00000483149.6:n.787C>G
ENST00000520403.1:n.829C>G
ENST00000520470.5:n.908C>G
ENST00000523407.1:n.710C>G
NM_198841.2:c.*61C>G	NP_942138.2:n.*61C>G
XM_005251736.2:c.919C>G	XP_005251793.1:n.919C>G
NM_001322224.2:c.*61C>G	NP_001309153.1:n.*61C>G
NM_198841.3:c.*61C>G	NP_942138.2:n.*61C>G
NR_136229.2:n.1131C>G
NR_136230.2:n.1252C>G
NR_136231.2:n.1845C>G
NR_136232.2:n.1057C>G
NR_136233.2:n.880C>G
NR_136234.2:n.914C>G
NR_136235.2:n.936C>G
NR_136236.2:n.1139C>G
NR_136237.2:n.1260C>G
NR_136238.2:n.1001C>G
NM_198841.4:c.*61C>G MANE Select	NP_942138.2:n.*61C>G
NM_001322224.3:c.*61C>G	NP_001309153.1:n.*61C>G
NR_136231.3:n.1825C>G
NR_136232.3:n.1054C>G
NR_136233.3:n.877C>G
NR_136234.3:n.911C>G
NR_136235.3:n.933C>G
NR_136236.3:n.1136C>G
NR_136237.3:n.1257C>G
NR_136238.3:n.998C>G