Canonical Allele Identifier: CA2788920985

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014555A>T , CM000672.2:g.89014555A>T	GRCh38
NC_000010.10:g.90774312A>T , CM000672.1:g.90774312A>T	GRCh37
NC_000010.9:g.90764292A>T	NCBI36
NG_009089.2:g.29025A>T , LRG_134:g.29025A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1422A>T
ENST00000355740.8:c.*436A>T	ENSP00000347979.3:n.*436A>T
ENST00000357339.7:c.*105A>T	ENSP00000349896.2:n.*105A>T
ENST00000371857.8:n.2658A>T
ENST00000460510.6:c.*105A>T	ENSP00000512812.1:n.*105A>T
ENST00000466081.6:n.2762A>T
ENST00000477270.6:c.*105A>T	ENSP00000512813.1:n.*105A>T
ENST00000479522.6:c.*542A>T	ENSP00000424113.1:n.*542A>T
ENST00000484444.6:c.*554A>T	ENSP00000420975.1:n.*554A>T
ENST00000488877.6:c.1004A>T	ENSP00000425159.1:n.1004A>T
ENST00000492756.7:c.*542A>T	ENSP00000422453.1:n.*542A>T
ENST00000494799.6:c.*105A>T	ENSP00000512834.1:n.*105A>T
ENST00000562983.3:c.*105A>T	ENSP00000512845.1:n.*105A>T
ENST00000612663.6:c.*515A>T	ENSP00000477997.3:n.*515A>T
ENST00000640140.2:n.1258A>T
ENST00000640250.2:n.612A>T
ENST00000640681.2:n.1217A>T
ENST00000696723.1:n.4746A>T
ENST00000696741.1:n.2751A>T
ENST00000696742.1:n.2478A>T
ENST00000696743.1:n.3881A>T
ENST00000696744.1:n.1152A>T
ENST00000696767.1:n.1447A>T
ENST00000696768.1:c.*436A>T	ENSP00000512859.1:n.*436A>T
ENST00000696769.1:n.2802A>T
ENST00000696771.1:c.*105A>T	ENSP00000512860.1:n.*105A>T
ENST00000696772.1:n.2716A>T
ENST00000696773.1:n.2455A>T
ENST00000696774.1:n.6223A>T
ENST00000696776.1:c.*105A>T	ENSP00000512861.1:n.*105A>T
ENST00000696777.1:n.2521A>T
ENST00000696778.1:n.1549A>T
ENST00000696779.1:c.*105A>T	ENSP00000512862.1:n.*105A>T
ENST00000696780.1:c.*105A>T	ENSP00000512863.1:n.*105A>T
ENST00000696781.1:c.*105A>T	ENSP00000512864.1:n.*105A>T
ENST00000696782.1:c.*515A>T	ENSP00000512865.1:n.*515A>T
ENST00000696783.1:n.2981A>T
ENST00000696992.1:n.2230A>T
ENST00000696995.1:n.4642A>T
ENST00000696996.1:n.2555A>T
ENST00000696997.1:c.*743A>T	ENSP00000513028.1:n.*743A>T
ENST00000696998.1:n.2367A>T
ENST00000696999.1:c.*105A>T	ENSP00000513029.1:n.*105A>T
ENST00000697036.1:c.*529A>T	ENSP00000513060.1:n.*529A>T
ENST00000697037.1:n.1148A>T
ENST00000697093.1:n.3349A>T
ENST00000697094.1:n.3696A>T
ENST00000697095.1:c.*2314A>T	ENSP00000513104.1:n.*2314A>T
ENST00000697096.1:n.2246A>T
ENST00000697097.1:c.*105A>T	ENSP00000513105.1:n.*105A>T
ENST00000562983.2:n.1299A>T
ENST00000690268.1:c.*105A>T	ENSP00000509810.1:n.*105A>T
ENST00000355740.7:c.*439A>T	ENSP00000347979.3:n.*439A>T
ENST00000640140.1:n.1285A>T
ENST00000640250.1:n.612A>T
ENST00000640681.1:n.1234A>T
ENST00000652046.1:c.*105A>T MANE Select	ENSP00000498466.1:n.*105A>T
ENST00000352159.8:c.*430A>T	ENSP00000345601.4:n.*430A>T
ENST00000355740.6:c.*105A>T	ENSP00000347979.2:n.*105A>T
ENST00000479522.5:c.*542A>T	ENSP00000424113.1:n.*542A>T
ENST00000484444.5:c.*554A>T	ENSP00000420975.1:n.*554A>T
ENST00000494410.5:c.*471A>T	ENSP00000423755.1:n.*471A>T
NM_000043.4:c.*105A>T , LRG_134t1:c.*105A>T	NP_000034.1:n.*105A>T
NM_152871.2:c.*105A>T	NP_690610.1:n.*105A>T
NM_152872.2:c.*425A>T	NP_690611.1:n.*425A>T
NR_028033.2:n.1287A>T
NR_028034.2:n.1149A>T
NR_028035.2:n.1212A>T
NR_028036.2:n.1350A>T
XM_006717819.2:c.*105A>T	XP_006717882.1:n.*105A>T
XM_011539764.1:c.*105A>T	XP_011538066.1:n.*105A>T
XM_011539765.1:c.*105A>T	XP_011538067.1:n.*105A>T
XM_011539766.1:c.*105A>T	XP_011538068.1:n.*105A>T
XM_011539767.1:c.*105A>T	XP_011538069.1:n.*105A>T
NM_000043.5:c.*105A>T	NP_000034.1:n.*105A>T
NM_001320619.1:c.*436A>T	NP_001307548.1:n.*436A>T
NM_152871.3:c.*105A>T	NP_690610.1:n.*105A>T
NM_152872.3:c.*425A>T	NP_690611.1:n.*425A>T
NR_028033.3:n.1259A>T
NR_028034.3:n.1121A>T
NR_028035.3:n.1184A>T
NR_028036.3:n.1322A>T
NR_135313.1:n.1239A>T
NR_135314.1:n.1422A>T
NR_135315.1:n.1175A>T
XM_006717819.3:c.*105A>T	XP_006717882.1:n.*105A>T
XM_011539764.2:c.*105A>T	XP_011538066.1:n.*105A>T
XM_011539765.2:c.*105A>T	XP_011538067.1:n.*105A>T
XM_011539766.2:c.*105A>T	XP_011538068.1:n.*105A>T
XM_011539767.3:c.*105A>T	XP_011538069.1:n.*105A>T
XR_945732.3:n.1181A>T
XR_945733.2:n.1118A>T
NM_000043.6:c.*105A>T MANE Select	NP_000034.1:n.*105A>T
NM_001320619.2:c.*436A>T	NP_001307548.1:n.*436A>T
NM_152871.4:c.*105A>T	NP_690610.1:n.*105A>T
NM_152872.4:c.*425A>T	NP_690611.1:n.*425A>T
NR_028033.4:n.1020A>T
NR_028034.4:n.882A>T
NR_028035.4:n.945A>T
NR_028036.4:n.1083A>T
NR_135313.2:n.1000A>T
NR_135314.2:n.1279A>T
NR_135315.2:n.1032A>T