Canonical Allele Identifier: CA1926639498

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014591G= , CM000672.2:g.89014591G=	GRCh38
NC_000010.10:g.90774348G= , CM000672.1:g.90774348G=	GRCh37
NC_000010.9:g.90764328G=	NCBI36
NG_009089.2:g.29061G= , LRG_134:g.29061G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1458G=
ENST00000355740.8:c.*472G=	ENSP00000347979.3:n.*472G=
ENST00000357339.7:c.*141G=	ENSP00000349896.2:n.*141G=
ENST00000371857.8:n.2694G=
ENST00000460510.6:c.*141G=	ENSP00000512812.1:n.*141G=
ENST00000466081.6:n.2798G=
ENST00000477270.6:c.*141G=	ENSP00000512813.1:n.*141G=
ENST00000488877.6:c.1040G=	ENSP00000425159.1:n.1040G=
ENST00000492756.7:c.*578G=	ENSP00000422453.1:n.*578G=
ENST00000494799.6:c.*141G=	ENSP00000512834.1:n.*141G=
ENST00000562983.3:c.*141G=	ENSP00000512845.1:n.*141G=
ENST00000612663.6:c.*551G=	ENSP00000477997.3:n.*551G=
ENST00000640140.2:n.1294G=
ENST00000640250.2:n.648G=
ENST00000640681.2:n.1253G=
ENST00000696723.1:n.4782G=
ENST00000696741.1:n.2787G=
ENST00000696742.1:n.2514G=
ENST00000696743.1:n.3917G=
ENST00000696744.1:n.1188G=
ENST00000696767.1:n.1483G=
ENST00000696768.1:c.*472G=	ENSP00000512859.1:n.*472G=
ENST00000696771.1:c.*141G=	ENSP00000512860.1:n.*141G=
ENST00000696772.1:n.2752G=
ENST00000696773.1:n.2491G=
ENST00000696774.1:n.6259G=
ENST00000696776.1:c.*141G=	ENSP00000512861.1:n.*141G=
ENST00000696777.1:n.2557G=
ENST00000696778.1:n.1585G=
ENST00000696779.1:c.*141G=	ENSP00000512862.1:n.*141G=
ENST00000696780.1:c.*141G=	ENSP00000512863.1:n.*141G=
ENST00000696781.1:c.*141G=	ENSP00000512864.1:n.*141G=
ENST00000696782.1:c.*551G=	ENSP00000512865.1:n.*551G=
ENST00000696783.1:n.3017G=
ENST00000696992.1:n.2266G=
ENST00000696995.1:n.4678G=
ENST00000696996.1:n.2591G=
ENST00000696997.1:c.*779G=	ENSP00000513028.1:n.*779G=
ENST00000696998.1:n.2403G=
ENST00000696999.1:c.*141G=	ENSP00000513029.1:n.*141G=
ENST00000697036.1:c.*565G=	ENSP00000513060.1:n.*565G=
ENST00000697037.1:n.1184G=
ENST00000697093.1:n.3385G=
ENST00000697094.1:n.3732G=
ENST00000697095.1:c.*2350G=	ENSP00000513104.1:n.*2350G=
ENST00000697096.1:n.2282G=
ENST00000697097.1:c.*141G=	ENSP00000513105.1:n.*141G=
ENST00000562983.2:n.1335G=
ENST00000690268.1:c.*141G=	ENSP00000509810.1:n.*141G=
ENST00000355740.7:c.*475G=	ENSP00000347979.3:n.*475G=
ENST00000640140.1:n.1321G=
ENST00000640250.1:n.648G=
ENST00000640681.1:n.1270G=
ENST00000652046.1:c.*141G= MANE Select	ENSP00000498466.1:n.*141G=
ENST00000352159.8:c.*466G=	ENSP00000345601.4:n.*466G=
ENST00000355740.6:c.*141G=	ENSP00000347979.2:n.*141G=
ENST00000484444.5:c.*590G=	ENSP00000420975.1:n.*590G=
NM_000043.4:c.*141G= , LRG_134t1:c.*141G=	NP_000034.1:n.*141G=
NM_152871.2:c.*141G=	NP_690610.1:n.*141G=
NM_152872.2:c.*461G=	NP_690611.1:n.*461G=
NR_028033.2:n.1323G=
NR_028034.2:n.1185G=
NR_028035.2:n.1248G=
NR_028036.2:n.1386G=
XM_006717819.2:c.*141G=	XP_006717882.1:n.*141G=
XM_011539764.1:c.*141G=	XP_011538066.1:n.*141G=
XM_011539765.1:c.*141G=	XP_011538067.1:n.*141G=
XM_011539766.1:c.*141G=	XP_011538068.1:n.*141G=
XM_011539767.1:c.*141G=	XP_011538069.1:n.*141G=
NM_000043.5:c.*141G=	NP_000034.1:n.*141G=
NM_001320619.1:c.*472G=	NP_001307548.1:n.*472G=
NM_152871.3:c.*141G=	NP_690610.1:n.*141G=
NM_152872.3:c.*461G=	NP_690611.1:n.*461G=
NR_028033.3:n.1295G=
NR_028034.3:n.1157G=
NR_028035.3:n.1220G=
NR_028036.3:n.1358G=
NR_135313.1:n.1275G=
NR_135314.1:n.1458G=
NR_135315.1:n.1211G=
XM_006717819.3:c.*141G=	XP_006717882.1:n.*141G=
XM_011539764.2:c.*141G=	XP_011538066.1:n.*141G=
XM_011539765.2:c.*141G=	XP_011538067.1:n.*141G=
XM_011539766.2:c.*141G=	XP_011538068.1:n.*141G=
XM_011539767.3:c.*141G=	XP_011538069.1:n.*141G=
XR_945732.3:n.1217G=
XR_945733.2:n.1154G=
NM_000043.6:c.*141G= MANE Select	NP_000034.1:n.*141G=
NM_001320619.2:c.*472G=	NP_001307548.1:n.*472G=
NM_152871.4:c.*141G=	NP_690610.1:n.*141G=
NM_152872.4:c.*461G=	NP_690611.1:n.*461G=
NR_028033.4:n.1056G=
NR_028034.4:n.918G=
NR_028035.4:n.981G=
NR_028036.4:n.1119G=
NR_135313.2:n.1036G=
NR_135314.2:n.1315G=
NR_135315.2:n.1068G=