Canonical Allele Identifier: CA2579384373

Gene: FAM120AOS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.93447548_93447549del , CM000671.2:g.93447548_93447549del	GRCh38
NC_000009.11:g.96209830_96209831del , CM000671.1:g.96209830_96209831del	GRCh37
NC_000009.10:g.95249651_95249652del	NCBI36
NG_054727.1:g.11056_11057del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375412.11:c.*65_*66del MANE Select	ENSP00000364561.5:n.*65_*66del
ENST00000649557.1:c.*65_*66del	ENSP00000496904.1:n.*65_*66del
ENST00000650398.1:n.859_860del
ENST00000375412.9:c.*65_*66del	ENSP00000364561.5:n.*65_*66del
ENST00000423591.5:c.*65_*66del	ENSP00000414298.1:n.*65_*66del
ENST00000428152.1:n.552_553del
ENST00000476484.5:c.*234_*235del	ENSP00000429212.1:n.*234_*235del
ENST00000479094.5:n.853_854del
ENST00000483056.5:n.658_659del
ENST00000483149.6:n.791_792del
ENST00000520403.1:n.833_834del
ENST00000520470.5:n.912_913del
ENST00000523407.1:n.714_715del
NM_198841.2:c.*65_*66del	NP_942138.2:n.*65_*66del
XM_005251736.2:c.923_924del	XP_005251793.1:n.923_924del
NM_001322224.2:c.*65_*66del	NP_001309153.1:n.*65_*66del
NM_198841.3:c.*65_*66del	NP_942138.2:n.*65_*66del
NR_136229.2:n.1135_1136del
NR_136230.2:n.1256_1257del
NR_136231.2:n.1849_1850del
NR_136232.2:n.1061_1062del
NR_136233.2:n.884_885del
NR_136234.2:n.918_919del
NR_136235.2:n.940_941del
NR_136236.2:n.1143_1144del
NR_136237.2:n.1264_1265del
NR_136238.2:n.1005_1006del
NM_198841.4:c.*65_*66del MANE Select	NP_942138.2:n.*65_*66del
NM_001322224.3:c.*65_*66del	NP_001309153.1:n.*65_*66del
NR_136231.3:n.1829_1830del
NR_136232.3:n.1058_1059del
NR_136233.3:n.881_882del
NR_136234.3:n.915_916del
NR_136235.3:n.937_938del
NR_136236.3:n.1140_1141del
NR_136237.3:n.1261_1262del
NR_136238.3:n.1002_1003del