Canonical Allele Identifier: CA2610079723

Gene: FAS

Linked Data

• gnomAD v4: 10-89014572-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014572A>C , CM000672.2:g.89014572A>C	GRCh38
NC_000010.10:g.90774329A>C , CM000672.1:g.90774329A>C	GRCh37
NC_000010.9:g.90764309A>C	NCBI36
NG_009089.2:g.29042A>C , LRG_134:g.29042A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1439A>C
ENST00000355740.8:c.*453A>C	ENSP00000347979.3:n.*453A>C
ENST00000357339.7:c.*122A>C	ENSP00000349896.2:n.*122A>C
ENST00000371857.8:n.2675A>C
ENST00000460510.6:c.*122A>C	ENSP00000512812.1:n.*122A>C
ENST00000466081.6:n.2779A>C
ENST00000477270.6:c.*122A>C	ENSP00000512813.1:n.*122A>C
ENST00000479522.6:c.*559A>C	ENSP00000424113.1:n.*559A>C
ENST00000484444.6:c.*571A>C	ENSP00000420975.1:n.*571A>C
ENST00000488877.6:c.1021A>C	ENSP00000425159.1:n.1021A>C
ENST00000492756.7:c.*559A>C	ENSP00000422453.1:n.*559A>C
ENST00000494799.6:c.*122A>C	ENSP00000512834.1:n.*122A>C
ENST00000562983.3:c.*122A>C	ENSP00000512845.1:n.*122A>C
ENST00000612663.6:c.*532A>C	ENSP00000477997.3:n.*532A>C
ENST00000640140.2:n.1275A>C
ENST00000640250.2:n.629A>C
ENST00000640681.2:n.1234A>C
ENST00000696723.1:n.4763A>C
ENST00000696741.1:n.2768A>C
ENST00000696742.1:n.2495A>C
ENST00000696743.1:n.3898A>C
ENST00000696744.1:n.1169A>C
ENST00000696767.1:n.1464A>C
ENST00000696768.1:c.*453A>C	ENSP00000512859.1:n.*453A>C
ENST00000696771.1:c.*122A>C	ENSP00000512860.1:n.*122A>C
ENST00000696772.1:n.2733A>C
ENST00000696773.1:n.2472A>C
ENST00000696774.1:n.6240A>C
ENST00000696776.1:c.*122A>C	ENSP00000512861.1:n.*122A>C
ENST00000696777.1:n.2538A>C
ENST00000696778.1:n.1566A>C
ENST00000696779.1:c.*122A>C	ENSP00000512862.1:n.*122A>C
ENST00000696780.1:c.*122A>C	ENSP00000512863.1:n.*122A>C
ENST00000696781.1:c.*122A>C	ENSP00000512864.1:n.*122A>C
ENST00000696782.1:c.*532A>C	ENSP00000512865.1:n.*532A>C
ENST00000696783.1:n.2998A>C
ENST00000696992.1:n.2247A>C
ENST00000696995.1:n.4659A>C
ENST00000696996.1:n.2572A>C
ENST00000696997.1:c.*760A>C	ENSP00000513028.1:n.*760A>C
ENST00000696998.1:n.2384A>C
ENST00000696999.1:c.*122A>C	ENSP00000513029.1:n.*122A>C
ENST00000697036.1:c.*546A>C	ENSP00000513060.1:n.*546A>C
ENST00000697037.1:n.1165A>C
ENST00000697093.1:n.3366A>C
ENST00000697094.1:n.3713A>C
ENST00000697095.1:c.*2331A>C	ENSP00000513104.1:n.*2331A>C
ENST00000697096.1:n.2263A>C
ENST00000697097.1:c.*122A>C	ENSP00000513105.1:n.*122A>C
ENST00000562983.2:n.1316A>C
ENST00000690268.1:c.*122A>C	ENSP00000509810.1:n.*122A>C
ENST00000355740.7:c.*456A>C	ENSP00000347979.3:n.*456A>C
ENST00000640140.1:n.1302A>C
ENST00000640250.1:n.629A>C
ENST00000640681.1:n.1251A>C
ENST00000652046.1:c.*122A>C MANE Select	ENSP00000498466.1:n.*122A>C
ENST00000352159.8:c.*447A>C	ENSP00000345601.4:n.*447A>C
ENST00000355740.6:c.*122A>C	ENSP00000347979.2:n.*122A>C
ENST00000479522.5:c.*559A>C	ENSP00000424113.1:n.*559A>C
ENST00000484444.5:c.*571A>C	ENSP00000420975.1:n.*571A>C
ENST00000494410.5:c.*488A>C	ENSP00000423755.1:n.*488A>C
NM_000043.4:c.*122A>C , LRG_134t1:c.*122A>C	NP_000034.1:n.*122A>C
NM_152871.2:c.*122A>C	NP_690610.1:n.*122A>C
NM_152872.2:c.*442A>C	NP_690611.1:n.*442A>C
NR_028033.2:n.1304A>C
NR_028034.2:n.1166A>C
NR_028035.2:n.1229A>C
NR_028036.2:n.1367A>C
XM_006717819.2:c.*122A>C	XP_006717882.1:n.*122A>C
XM_011539764.1:c.*122A>C	XP_011538066.1:n.*122A>C
XM_011539765.1:c.*122A>C	XP_011538067.1:n.*122A>C
XM_011539766.1:c.*122A>C	XP_011538068.1:n.*122A>C
XM_011539767.1:c.*122A>C	XP_011538069.1:n.*122A>C
NM_000043.5:c.*122A>C	NP_000034.1:n.*122A>C
NM_001320619.1:c.*453A>C	NP_001307548.1:n.*453A>C
NM_152871.3:c.*122A>C	NP_690610.1:n.*122A>C
NM_152872.3:c.*442A>C	NP_690611.1:n.*442A>C
NR_028033.3:n.1276A>C
NR_028034.3:n.1138A>C
NR_028035.3:n.1201A>C
NR_028036.3:n.1339A>C
NR_135313.1:n.1256A>C
NR_135314.1:n.1439A>C
NR_135315.1:n.1192A>C
XM_006717819.3:c.*122A>C	XP_006717882.1:n.*122A>C
XM_011539764.2:c.*122A>C	XP_011538066.1:n.*122A>C
XM_011539765.2:c.*122A>C	XP_011538067.1:n.*122A>C
XM_011539766.2:c.*122A>C	XP_011538068.1:n.*122A>C
XM_011539767.3:c.*122A>C	XP_011538069.1:n.*122A>C
XR_945732.3:n.1198A>C
XR_945733.2:n.1135A>C
NM_000043.6:c.*122A>C MANE Select	NP_000034.1:n.*122A>C
NM_001320619.2:c.*453A>C	NP_001307548.1:n.*453A>C
NM_152871.4:c.*122A>C	NP_690610.1:n.*122A>C
NM_152872.4:c.*442A>C	NP_690611.1:n.*442A>C
NR_028033.4:n.1037A>C
NR_028034.4:n.899A>C
NR_028035.4:n.962A>C
NR_028036.4:n.1100A>C
NR_135313.2:n.1017A>C
NR_135314.2:n.1296A>C
NR_135315.2:n.1049A>C