Canonical Allele Identifier: CA2610079719

Gene: FAS

Linked Data

• gnomAD v4: 10-89014569-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014569C>A , CM000672.2:g.89014569C>A	GRCh38
NC_000010.10:g.90774326C>A , CM000672.1:g.90774326C>A	GRCh37
NC_000010.9:g.90764306C>A	NCBI36
NG_009089.2:g.29039C>A , LRG_134:g.29039C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1436C>A
ENST00000355740.8:c.*450C>A	ENSP00000347979.3:n.*450C>A
ENST00000357339.7:c.*119C>A	ENSP00000349896.2:n.*119C>A
ENST00000371857.8:n.2672C>A
ENST00000460510.6:c.*119C>A	ENSP00000512812.1:n.*119C>A
ENST00000466081.6:n.2776C>A
ENST00000477270.6:c.*119C>A	ENSP00000512813.1:n.*119C>A
ENST00000479522.6:c.*556C>A	ENSP00000424113.1:n.*556C>A
ENST00000484444.6:c.*568C>A	ENSP00000420975.1:n.*568C>A
ENST00000488877.6:c.1018C>A	ENSP00000425159.1:n.1018C>A
ENST00000492756.7:c.*556C>A	ENSP00000422453.1:n.*556C>A
ENST00000494799.6:c.*119C>A	ENSP00000512834.1:n.*119C>A
ENST00000562983.3:c.*119C>A	ENSP00000512845.1:n.*119C>A
ENST00000612663.6:c.*529C>A	ENSP00000477997.3:n.*529C>A
ENST00000640140.2:n.1272C>A
ENST00000640250.2:n.626C>A
ENST00000640681.2:n.1231C>A
ENST00000696723.1:n.4760C>A
ENST00000696741.1:n.2765C>A
ENST00000696742.1:n.2492C>A
ENST00000696743.1:n.3895C>A
ENST00000696744.1:n.1166C>A
ENST00000696767.1:n.1461C>A
ENST00000696768.1:c.*450C>A	ENSP00000512859.1:n.*450C>A
ENST00000696771.1:c.*119C>A	ENSP00000512860.1:n.*119C>A
ENST00000696772.1:n.2730C>A
ENST00000696773.1:n.2469C>A
ENST00000696774.1:n.6237C>A
ENST00000696776.1:c.*119C>A	ENSP00000512861.1:n.*119C>A
ENST00000696777.1:n.2535C>A
ENST00000696778.1:n.1563C>A
ENST00000696779.1:c.*119C>A	ENSP00000512862.1:n.*119C>A
ENST00000696780.1:c.*119C>A	ENSP00000512863.1:n.*119C>A
ENST00000696781.1:c.*119C>A	ENSP00000512864.1:n.*119C>A
ENST00000696782.1:c.*529C>A	ENSP00000512865.1:n.*529C>A
ENST00000696783.1:n.2995C>A
ENST00000696992.1:n.2244C>A
ENST00000696995.1:n.4656C>A
ENST00000696996.1:n.2569C>A
ENST00000696997.1:c.*757C>A	ENSP00000513028.1:n.*757C>A
ENST00000696998.1:n.2381C>A
ENST00000696999.1:c.*119C>A	ENSP00000513029.1:n.*119C>A
ENST00000697036.1:c.*543C>A	ENSP00000513060.1:n.*543C>A
ENST00000697037.1:n.1162C>A
ENST00000697093.1:n.3363C>A
ENST00000697094.1:n.3710C>A
ENST00000697095.1:c.*2328C>A	ENSP00000513104.1:n.*2328C>A
ENST00000697096.1:n.2260C>A
ENST00000697097.1:c.*119C>A	ENSP00000513105.1:n.*119C>A
ENST00000562983.2:n.1313C>A
ENST00000690268.1:c.*119C>A	ENSP00000509810.1:n.*119C>A
ENST00000355740.7:c.*453C>A	ENSP00000347979.3:n.*453C>A
ENST00000640140.1:n.1299C>A
ENST00000640250.1:n.626C>A
ENST00000640681.1:n.1248C>A
ENST00000652046.1:c.*119C>A MANE Select	ENSP00000498466.1:n.*119C>A
ENST00000352159.8:c.*444C>A	ENSP00000345601.4:n.*444C>A
ENST00000355740.6:c.*119C>A	ENSP00000347979.2:n.*119C>A
ENST00000479522.5:c.*556C>A	ENSP00000424113.1:n.*556C>A
ENST00000484444.5:c.*568C>A	ENSP00000420975.1:n.*568C>A
ENST00000494410.5:c.*485C>A	ENSP00000423755.1:n.*485C>A
NM_000043.4:c.*119C>A , LRG_134t1:c.*119C>A	NP_000034.1:n.*119C>A
NM_152871.2:c.*119C>A	NP_690610.1:n.*119C>A
NM_152872.2:c.*439C>A	NP_690611.1:n.*439C>A
NR_028033.2:n.1301C>A
NR_028034.2:n.1163C>A
NR_028035.2:n.1226C>A
NR_028036.2:n.1364C>A
XM_006717819.2:c.*119C>A	XP_006717882.1:n.*119C>A
XM_011539764.1:c.*119C>A	XP_011538066.1:n.*119C>A
XM_011539765.1:c.*119C>A	XP_011538067.1:n.*119C>A
XM_011539766.1:c.*119C>A	XP_011538068.1:n.*119C>A
XM_011539767.1:c.*119C>A	XP_011538069.1:n.*119C>A
NM_000043.5:c.*119C>A	NP_000034.1:n.*119C>A
NM_001320619.1:c.*450C>A	NP_001307548.1:n.*450C>A
NM_152871.3:c.*119C>A	NP_690610.1:n.*119C>A
NM_152872.3:c.*439C>A	NP_690611.1:n.*439C>A
NR_028033.3:n.1273C>A
NR_028034.3:n.1135C>A
NR_028035.3:n.1198C>A
NR_028036.3:n.1336C>A
NR_135313.1:n.1253C>A
NR_135314.1:n.1436C>A
NR_135315.1:n.1189C>A
XM_006717819.3:c.*119C>A	XP_006717882.1:n.*119C>A
XM_011539764.2:c.*119C>A	XP_011538066.1:n.*119C>A
XM_011539765.2:c.*119C>A	XP_011538067.1:n.*119C>A
XM_011539766.2:c.*119C>A	XP_011538068.1:n.*119C>A
XM_011539767.3:c.*119C>A	XP_011538069.1:n.*119C>A
XR_945732.3:n.1195C>A
XR_945733.2:n.1132C>A
NM_000043.6:c.*119C>A MANE Select	NP_000034.1:n.*119C>A
NM_001320619.2:c.*450C>A	NP_001307548.1:n.*450C>A
NM_152871.4:c.*119C>A	NP_690610.1:n.*119C>A
NM_152872.4:c.*439C>A	NP_690611.1:n.*439C>A
NR_028033.4:n.1034C>A
NR_028034.4:n.896C>A
NR_028035.4:n.959C>A
NR_028036.4:n.1097C>A
NR_135313.2:n.1014C>A
NR_135314.2:n.1293C>A
NR_135315.2:n.1046C>A