Canonical Allele Identifier: CA377510004

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774071A>C (hg19) ; chr10:g.89014314A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014314A>C , CM000672.2:g.89014314A>C	GRCh38
NC_000010.10:g.90774071A>C , CM000672.1:g.90774071A>C	GRCh37
NC_000010.9:g.90764051A>C	NCBI36
NG_009089.2:g.28784A>C , LRG_134:g.28784A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1181A>C
ENST00000355740.8:c.*195A>C	ENSP00000347979.3:n.*195A>C
ENST00000357339.7:c.809A>C	ENSP00000349896.2:p.Tyr270Ser
ENST00000371857.8:n.2417A>C
ENST00000460510.6:c.155A>C	ENSP00000512812.1:p.Tyr52Ser
ENST00000466081.6:n.2521A>C
ENST00000477270.6:c.917A>C	ENSP00000512813.1:p.Tyr306Ser
ENST00000479522.6:c.*301A>C	ENSP00000424113.1:n.*301A>C
ENST00000484444.6:c.*313A>C	ENSP00000420975.1:n.*313A>C
ENST00000488877.6:c.763A>C	ENSP00000425159.1:n.763A>C
ENST00000492756.7:c.*301A>C	ENSP00000422453.1:n.*301A>C
ENST00000494799.6:c.155A>C	ENSP00000512834.1:p.Tyr52Ser
ENST00000562983.3:c.155A>C	ENSP00000512845.1:p.Tyr52Ser
ENST00000612663.6:c.*274A>C	ENSP00000477997.3:n.*274A>C
ENST00000640140.2:n.1017A>C
ENST00000640250.2:n.371A>C
ENST00000640681.2:n.976A>C
ENST00000696723.1:n.4505A>C
ENST00000696741.1:n.2510A>C
ENST00000696742.1:n.2237A>C
ENST00000696743.1:n.3640A>C
ENST00000696744.1:n.911A>C
ENST00000696767.1:n.1206A>C
ENST00000696768.1:c.*195A>C	ENSP00000512859.1:n.*195A>C
ENST00000696769.1:n.2561A>C
ENST00000696771.1:c.155A>C	ENSP00000512860.1:p.Tyr52Ser
ENST00000696772.1:n.2475A>C
ENST00000696773.1:n.2214A>C
ENST00000696774.1:n.5982A>C
ENST00000696776.1:c.965A>C	ENSP00000512861.1:p.Tyr322Ser
ENST00000696777.1:n.2280A>C
ENST00000696778.1:n.1308A>C
ENST00000696779.1:c.479A>C	ENSP00000512862.1:p.Tyr160Ser
ENST00000696780.1:c.902A>C	ENSP00000512863.1:p.Tyr301Ser
ENST00000696781.1:c.617A>C	ENSP00000512864.1:p.Tyr206Ser
ENST00000696782.1:c.*274A>C	ENSP00000512865.1:n.*274A>C
ENST00000696783.1:n.2740A>C
ENST00000696992.1:n.1989A>C
ENST00000696995.1:n.4401A>C
ENST00000696996.1:n.2314A>C
ENST00000696997.1:c.*502A>C	ENSP00000513028.1:n.*502A>C
ENST00000696998.1:n.2126A>C
ENST00000696999.1:c.155A>C	ENSP00000513029.1:p.Tyr52Ser
ENST00000697036.1:c.*288A>C	ENSP00000513060.1:n.*288A>C
ENST00000697037.1:n.907A>C
ENST00000697093.1:n.3108A>C
ENST00000697094.1:n.3455A>C
ENST00000697095.1:c.*2073A>C	ENSP00000513104.1:n.*2073A>C
ENST00000697096.1:n.2005A>C
ENST00000697097.1:c.155A>C	ENSP00000513105.1:p.Tyr52Ser
ENST00000562983.2:n.1058A>C
ENST00000690268.1:c.953A>C	ENSP00000509810.1:p.Tyr318Ser
ENST00000355740.7:c.*198A>C	ENSP00000347979.3:n.*198A>C
ENST00000612663.5:c.*274A>C	ENSP00000477997.3:n.*274A>C
ENST00000640140.1:n.1044A>C
ENST00000640250.1:n.371A>C
ENST00000640681.1:n.993A>C
ENST00000652046.1:c.872A>C MANE Select	ENSP00000498466.1:p.Tyr291Ser
ENST00000352159.8:c.*189A>C	ENSP00000345601.4:n.*189A>C
ENST00000355279.2:c.847A>C	ENSP00000347426.2:n.847A>C
ENST00000355740.6:c.872A>C	ENSP00000347979.2:p.Tyr291Ser
ENST00000357339.6:c.809A>C	ENSP00000349896.2:p.Tyr270Ser
ENST00000479522.5:c.*301A>C	ENSP00000424113.1:n.*301A>C
ENST00000484444.5:c.*313A>C	ENSP00000420975.1:n.*313A>C
ENST00000488877.5:c.*313A>C	ENSP00000425159.1:n.*313A>C
ENST00000492756.5:c.700A>C	ENSP00000422453.1:n.700A>C
ENST00000494410.5:c.*230A>C	ENSP00000423755.1:n.*230A>C
ENST00000612663.4:c.*219A>C	ENSP00000477997.2:n.*219A>C
NM_000043.4:c.872A>C , LRG_134t1:c.872A>C	NP_000034.1:p.Tyr291Ser
NM_152871.2:c.809A>C	NP_690610.1:p.Tyr270Ser
NM_152872.2:c.*184A>C	NP_690611.1:n.*184A>C
NR_028033.2:n.1046A>C
NR_028034.2:n.908A>C
NR_028035.2:n.971A>C
NR_028036.2:n.1109A>C
XM_006717819.2:c.953A>C	XP_006717882.1:p.Tyr318Ser
XM_011539764.1:c.1034A>C	XP_011538066.1:p.Tyr345Ser
XM_011539765.1:c.971A>C	XP_011538067.1:p.Tyr324Ser
XM_011539766.1:c.953A>C	XP_011538068.1:p.Tyr318Ser
XM_011539767.1:c.917A>C	XP_011538069.1:p.Tyr306Ser
XR_945732.1:n.940A>C
XR_945733.1:n.877A>C
NM_000043.5:c.872A>C	NP_000034.1:p.Tyr291Ser
NM_001320619.1:c.*195A>C	NP_001307548.1:n.*195A>C
NM_152871.3:c.809A>C	NP_690610.1:p.Tyr270Ser
NM_152872.3:c.*184A>C	NP_690611.1:n.*184A>C
NR_028033.3:n.1018A>C
NR_028034.3:n.880A>C
NR_028035.3:n.943A>C
NR_028036.3:n.1081A>C
NR_135313.1:n.998A>C
NR_135314.1:n.1181A>C
NR_135315.1:n.934A>C
XM_006717819.3:c.953A>C	XP_006717882.1:p.Tyr318Ser
XM_011539764.2:c.1034A>C	XP_011538066.1:p.Tyr345Ser
XM_011539765.2:c.971A>C	XP_011538067.1:p.Tyr324Ser
XM_011539766.2:c.953A>C	XP_011538068.1:p.Tyr318Ser
XM_011539767.3:c.917A>C	XP_011538069.1:p.Tyr306Ser
XR_945732.3:n.940A>C
XR_945733.2:n.877A>C
NM_000043.6:c.872A>C MANE Select	NP_000034.1:p.Tyr291Ser
NM_001320619.2:c.*195A>C	NP_001307548.1:n.*195A>C
NM_152871.4:c.809A>C	NP_690610.1:p.Tyr270Ser
NM_152872.4:c.*184A>C	NP_690611.1:n.*184A>C
NR_028033.4:n.779A>C
NR_028034.4:n.641A>C
NR_028035.4:n.704A>C
NR_028036.4:n.842A>C
NR_135313.2:n.759A>C
NR_135314.2:n.1038A>C
NR_135315.2:n.791A>C