Canonical Allele Identifier: CA1864666302

Gene: FAM120AOS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.93447561G= , CM000671.2:g.93447561G=	GRCh38
NC_000009.11:g.96209843G= , CM000671.1:g.96209843G=	GRCh37
NC_000009.10:g.95249664G=	NCBI36
NG_054727.1:g.11041C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375412.11:c.*50C= MANE Select	ENSP00000364561.5:n.*50C=
ENST00000649557.1:c.*50C=	ENSP00000496904.1:n.*50C=
ENST00000650398.1:n.844C=
ENST00000375412.9:c.*50C=	ENSP00000364561.5:n.*50C=
ENST00000423591.5:c.*50C=	ENSP00000414298.1:n.*50C=
ENST00000428152.1:n.537C=
ENST00000476484.5:c.*219C=	ENSP00000429212.1:n.*219C=
ENST00000479094.5:n.838C=
ENST00000483056.5:n.643C=
ENST00000483149.6:n.776C=
ENST00000520403.1:n.818C=
ENST00000520470.5:n.897C=
ENST00000523407.1:n.699C=
NM_198841.2:c.*50C=	NP_942138.2:n.*50C=
XM_005251736.2:c.908C=	XP_005251793.1:n.908C=
NM_001322224.2:c.*50C=	NP_001309153.1:n.*50C=
NM_198841.3:c.*50C=	NP_942138.2:n.*50C=
NR_136229.2:n.1120C=
NR_136230.2:n.1241C=
NR_136231.2:n.1834C=
NR_136232.2:n.1046C=
NR_136233.2:n.869C=
NR_136234.2:n.903C=
NR_136235.2:n.925C=
NR_136236.2:n.1128C=
NR_136237.2:n.1249C=
NR_136238.2:n.990C=
NM_198841.4:c.*50C= MANE Select	NP_942138.2:n.*50C=
NM_001322224.3:c.*50C=	NP_001309153.1:n.*50C=
NR_136231.3:n.1814C=
NR_136232.3:n.1043C=
NR_136233.3:n.866C=
NR_136234.3:n.900C=
NR_136235.3:n.922C=
NR_136236.3:n.1125C=
NR_136237.3:n.1246C=
NR_136238.3:n.987C=