Canonical Allele Identifier: CA2788920995

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014683A>C , CM000672.2:g.89014683A>C	GRCh38
NC_000010.10:g.90774440A>C , CM000672.1:g.90774440A>C	GRCh37
NC_000010.9:g.90764420A>C	NCBI36
NG_009089.2:g.29153A>C , LRG_134:g.29153A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1550A>C
ENST00000355740.8:c.*564A>C	ENSP00000347979.3:n.*564A>C
ENST00000357339.7:c.*233A>C	ENSP00000349896.2:n.*233A>C
ENST00000371857.8:n.2786A>C
ENST00000460510.6:c.*233A>C	ENSP00000512812.1:n.*233A>C
ENST00000466081.6:n.2890A>C
ENST00000477270.6:c.*233A>C	ENSP00000512813.1:n.*233A>C
ENST00000492756.7:c.*670A>C	ENSP00000422453.1:n.*670A>C
ENST00000494799.6:c.*233A>C	ENSP00000512834.1:n.*233A>C
ENST00000562983.3:c.*233A>C	ENSP00000512845.1:n.*233A>C
ENST00000612663.6:c.*643A>C	ENSP00000477997.3:n.*643A>C
ENST00000640140.2:n.1386A>C
ENST00000640250.2:n.740A>C
ENST00000640681.2:n.1345A>C
ENST00000696723.1:n.4874A>C
ENST00000696741.1:n.2879A>C
ENST00000696742.1:n.2606A>C
ENST00000696743.1:n.4009A>C
ENST00000696744.1:n.1280A>C
ENST00000696767.1:n.1575A>C
ENST00000696768.1:c.*564A>C	ENSP00000512859.1:n.*564A>C
ENST00000696771.1:c.*233A>C	ENSP00000512860.1:n.*233A>C
ENST00000696772.1:n.2844A>C
ENST00000696773.1:n.2583A>C
ENST00000696774.1:n.6351A>C
ENST00000696776.1:c.*233A>C	ENSP00000512861.1:n.*233A>C
ENST00000696777.1:n.2649A>C
ENST00000696778.1:n.1677A>C
ENST00000696779.1:c.*233A>C	ENSP00000512862.1:n.*233A>C
ENST00000696780.1:c.*233A>C	ENSP00000512863.1:n.*233A>C
ENST00000696781.1:c.*233A>C	ENSP00000512864.1:n.*233A>C
ENST00000696782.1:c.*643A>C	ENSP00000512865.1:n.*643A>C
ENST00000696783.1:n.3109A>C
ENST00000696992.1:n.2358A>C
ENST00000696995.1:n.4770A>C
ENST00000696996.1:n.2683A>C
ENST00000696997.1:c.*871A>C	ENSP00000513028.1:n.*871A>C
ENST00000696998.1:n.2495A>C
ENST00000696999.1:c.*233A>C	ENSP00000513029.1:n.*233A>C
ENST00000697036.1:c.*657A>C	ENSP00000513060.1:n.*657A>C
ENST00000697037.1:n.1276A>C
ENST00000697093.1:n.3477A>C
ENST00000697094.1:n.3824A>C
ENST00000697095.1:c.*2442A>C	ENSP00000513104.1:n.*2442A>C
ENST00000697096.1:n.2374A>C
ENST00000697097.1:c.*233A>C	ENSP00000513105.1:n.*233A>C
ENST00000562983.2:n.1427A>C
ENST00000690268.1:c.*233A>C	ENSP00000509810.1:n.*233A>C
ENST00000355740.7:c.*567A>C	ENSP00000347979.3:n.*567A>C
ENST00000640140.1:n.1413A>C
ENST00000640250.1:n.740A>C
ENST00000640681.1:n.1362A>C
ENST00000652046.1:c.*233A>C MANE Select	ENSP00000498466.1:n.*233A>C
ENST00000352159.8:c.*558A>C	ENSP00000345601.4:n.*558A>C
ENST00000355740.6:c.*233A>C	ENSP00000347979.2:n.*233A>C
NM_000043.4:c.*233A>C , LRG_134t1:c.*233A>C	NP_000034.1:n.*233A>C
NM_152871.2:c.*233A>C	NP_690610.1:n.*233A>C
NM_152872.2:c.*553A>C	NP_690611.1:n.*553A>C
NR_028033.2:n.1415A>C
NR_028034.2:n.1277A>C
NR_028035.2:n.1340A>C
NR_028036.2:n.1478A>C
XM_006717819.2:c.*233A>C	XP_006717882.1:n.*233A>C
XM_011539764.1:c.*233A>C	XP_011538066.1:n.*233A>C
XM_011539765.1:c.*233A>C	XP_011538067.1:n.*233A>C
XM_011539766.1:c.*233A>C	XP_011538068.1:n.*233A>C
XM_011539767.1:c.*233A>C	XP_011538069.1:n.*233A>C
NM_000043.5:c.*233A>C	NP_000034.1:n.*233A>C
NM_001320619.1:c.*564A>C	NP_001307548.1:n.*564A>C
NM_152871.3:c.*233A>C	NP_690610.1:n.*233A>C
NM_152872.3:c.*553A>C	NP_690611.1:n.*553A>C
NR_028033.3:n.1387A>C
NR_028034.3:n.1249A>C
NR_028035.3:n.1312A>C
NR_028036.3:n.1450A>C
NR_135313.1:n.1367A>C
NR_135314.1:n.1550A>C
NR_135315.1:n.1303A>C
XM_006717819.3:c.*233A>C	XP_006717882.1:n.*233A>C
XM_011539764.2:c.*233A>C	XP_011538066.1:n.*233A>C
XM_011539765.2:c.*233A>C	XP_011538067.1:n.*233A>C
XM_011539766.2:c.*233A>C	XP_011538068.1:n.*233A>C
XM_011539767.3:c.*233A>C	XP_011538069.1:n.*233A>C
XR_945732.3:n.1309A>C
XR_945733.2:n.1246A>C
NM_000043.6:c.*233A>C MANE Select	NP_000034.1:n.*233A>C
NM_001320619.2:c.*564A>C	NP_001307548.1:n.*564A>C
NM_152871.4:c.*233A>C	NP_690610.1:n.*233A>C
NM_152872.4:c.*553A>C	NP_690611.1:n.*553A>C
NR_028033.4:n.1148A>C
NR_028034.4:n.1010A>C
NR_028035.4:n.1073A>C
NR_028036.4:n.1211A>C
NR_135313.2:n.1128A>C
NR_135314.2:n.1407A>C
NR_135315.2:n.1160A>C