Canonical Allele Identifier: CA1864666290

Gene: FAM120AOS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.93447557_93447568delinsATCAGGGTGGTT , CM000671.2:g.93447557_93447568delinsATCAGGGTGGTT	GRCh38
NC_000009.11:g.96209839_96209850delinsATCAGGGTGGTT , CM000671.1:g.96209839_96209850delinsATCAGGGTGGTT	GRCh37
NC_000009.10:g.95249660_95249671delinsATCAGGGTGGTT	NCBI36
NG_054727.1:g.11034_11045delinsAACCACCCTGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375412.11:c.*43_*54delinsAACCACCCTGAT MANE Select	ENSP00000364561.5:n.*43_*54delinsAACCACCCTGAT
ENST00000649557.1:c.*43_*54delinsAACCACCCTGAT	ENSP00000496904.1:n.*43_*54delinsAACCACCCTGAT
ENST00000650398.1:n.837_848delinsAACCACCCTGAT
ENST00000375412.9:c.*43_*54delinsAACCACCCTGAT	ENSP00000364561.5:n.*43_*54delinsAACCACCCTGAT
ENST00000423591.5:c.*43_*54delinsAACCACCCTGAT	ENSP00000414298.1:n.*43_*54delinsAACCACCCTGAT
ENST00000428152.1:n.530_541delinsAACCACCCTGAT
ENST00000476484.5:c.*212_*223delinsAACCACCCTGAT	ENSP00000429212.1:n.*212_*223delinsAACCACCCTGAT
ENST00000479094.5:n.831_842delinsAACCACCCTGAT
ENST00000483056.5:n.636_647delinsAACCACCCTGAT
ENST00000483149.6:n.769_780delinsAACCACCCTGAT
ENST00000520403.1:n.811_822delinsAACCACCCTGAT
ENST00000520470.5:n.890_901delinsAACCACCCTGAT
ENST00000523407.1:n.692_703delinsAACCACCCTGAT
NM_198841.2:c.*43_*54delinsAACCACCCTGAT	NP_942138.2:n.*43_*54delinsAACCACCCTGAT
XM_005251736.2:c.901_912delinsAACCACCCTGAT	XP_005251793.1:n.901_912delinsAACCACCCTGAT
NM_001322224.2:c.*43_*54delinsAACCACCCTGAT	NP_001309153.1:n.*43_*54delinsAACCACCCTGAT
NM_198841.3:c.*43_*54delinsAACCACCCTGAT	NP_942138.2:n.*43_*54delinsAACCACCCTGAT
NR_136229.2:n.1113_1124delinsAACCACCCTGAT
NR_136230.2:n.1234_1245delinsAACCACCCTGAT
NR_136231.2:n.1827_1838delinsAACCACCCTGAT
NR_136232.2:n.1039_1050delinsAACCACCCTGAT
NR_136233.2:n.862_873delinsAACCACCCTGAT
NR_136234.2:n.896_907delinsAACCACCCTGAT
NR_136235.2:n.918_929delinsAACCACCCTGAT
NR_136236.2:n.1121_1132delinsAACCACCCTGAT
NR_136237.2:n.1242_1253delinsAACCACCCTGAT
NR_136238.2:n.983_994delinsAACCACCCTGAT
NM_198841.4:c.*43_*54delinsAACCACCCTGAT MANE Select	NP_942138.2:n.*43_*54delinsAACCACCCTGAT
NM_001322224.3:c.*43_*54delinsAACCACCCTGAT	NP_001309153.1:n.*43_*54delinsAACCACCCTGAT
NR_136231.3:n.1807_1818delinsAACCACCCTGAT
NR_136232.3:n.1036_1047delinsAACCACCCTGAT
NR_136233.3:n.859_870delinsAACCACCCTGAT
NR_136234.3:n.893_904delinsAACCACCCTGAT
NR_136235.3:n.915_926delinsAACCACCCTGAT
NR_136236.3:n.1118_1129delinsAACCACCCTGAT
NR_136237.3:n.1239_1250delinsAACCACCCTGAT
NR_136238.3:n.980_991delinsAACCACCCTGAT