Canonical Allele Identifier: CA2610079754

Gene: FAS

Linked Data

• gnomAD v4: 10-89014617-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014617T>C , CM000672.2:g.89014617T>C	GRCh38
NC_000010.10:g.90774374T>C , CM000672.1:g.90774374T>C	GRCh37
NC_000010.9:g.90764354T>C	NCBI36
NG_009089.2:g.29087T>C , LRG_134:g.29087T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1484T>C
ENST00000355740.8:c.*498T>C	ENSP00000347979.3:n.*498T>C
ENST00000357339.7:c.*167T>C	ENSP00000349896.2:n.*167T>C
ENST00000371857.8:n.2720T>C
ENST00000460510.6:c.*167T>C	ENSP00000512812.1:n.*167T>C
ENST00000466081.6:n.2824T>C
ENST00000477270.6:c.*167T>C	ENSP00000512813.1:n.*167T>C
ENST00000488877.6:c.1066T>C	ENSP00000425159.1:n.1066T>C
ENST00000492756.7:c.*604T>C	ENSP00000422453.1:n.*604T>C
ENST00000494799.6:c.*167T>C	ENSP00000512834.1:n.*167T>C
ENST00000562983.3:c.*167T>C	ENSP00000512845.1:n.*167T>C
ENST00000612663.6:c.*577T>C	ENSP00000477997.3:n.*577T>C
ENST00000640140.2:n.1320T>C
ENST00000640250.2:n.674T>C
ENST00000640681.2:n.1279T>C
ENST00000696723.1:n.4808T>C
ENST00000696741.1:n.2813T>C
ENST00000696742.1:n.2540T>C
ENST00000696743.1:n.3943T>C
ENST00000696744.1:n.1214T>C
ENST00000696767.1:n.1509T>C
ENST00000696768.1:c.*498T>C	ENSP00000512859.1:n.*498T>C
ENST00000696771.1:c.*167T>C	ENSP00000512860.1:n.*167T>C
ENST00000696772.1:n.2778T>C
ENST00000696773.1:n.2517T>C
ENST00000696774.1:n.6285T>C
ENST00000696776.1:c.*167T>C	ENSP00000512861.1:n.*167T>C
ENST00000696777.1:n.2583T>C
ENST00000696778.1:n.1611T>C
ENST00000696779.1:c.*167T>C	ENSP00000512862.1:n.*167T>C
ENST00000696780.1:c.*167T>C	ENSP00000512863.1:n.*167T>C
ENST00000696781.1:c.*167T>C	ENSP00000512864.1:n.*167T>C
ENST00000696782.1:c.*577T>C	ENSP00000512865.1:n.*577T>C
ENST00000696783.1:n.3043T>C
ENST00000696992.1:n.2292T>C
ENST00000696995.1:n.4704T>C
ENST00000696996.1:n.2617T>C
ENST00000696997.1:c.*805T>C	ENSP00000513028.1:n.*805T>C
ENST00000696998.1:n.2429T>C
ENST00000696999.1:c.*167T>C	ENSP00000513029.1:n.*167T>C
ENST00000697036.1:c.*591T>C	ENSP00000513060.1:n.*591T>C
ENST00000697037.1:n.1210T>C
ENST00000697093.1:n.3411T>C
ENST00000697094.1:n.3758T>C
ENST00000697095.1:c.*2376T>C	ENSP00000513104.1:n.*2376T>C
ENST00000697096.1:n.2308T>C
ENST00000697097.1:c.*167T>C	ENSP00000513105.1:n.*167T>C
ENST00000562983.2:n.1361T>C
ENST00000690268.1:c.*167T>C	ENSP00000509810.1:n.*167T>C
ENST00000355740.7:c.*501T>C	ENSP00000347979.3:n.*501T>C
ENST00000640140.1:n.1347T>C
ENST00000640250.1:n.674T>C
ENST00000640681.1:n.1296T>C
ENST00000652046.1:c.*167T>C MANE Select	ENSP00000498466.1:n.*167T>C
ENST00000352159.8:c.*492T>C	ENSP00000345601.4:n.*492T>C
ENST00000355740.6:c.*167T>C	ENSP00000347979.2:n.*167T>C
ENST00000484444.5:c.*616T>C	ENSP00000420975.1:n.*616T>C
NM_000043.4:c.*167T>C , LRG_134t1:c.*167T>C	NP_000034.1:n.*167T>C
NM_152871.2:c.*167T>C	NP_690610.1:n.*167T>C
NM_152872.2:c.*487T>C	NP_690611.1:n.*487T>C
NR_028033.2:n.1349T>C
NR_028034.2:n.1211T>C
NR_028035.2:n.1274T>C
NR_028036.2:n.1412T>C
XM_006717819.2:c.*167T>C	XP_006717882.1:n.*167T>C
XM_011539764.1:c.*167T>C	XP_011538066.1:n.*167T>C
XM_011539765.1:c.*167T>C	XP_011538067.1:n.*167T>C
XM_011539766.1:c.*167T>C	XP_011538068.1:n.*167T>C
XM_011539767.1:c.*167T>C	XP_011538069.1:n.*167T>C
NM_000043.5:c.*167T>C	NP_000034.1:n.*167T>C
NM_001320619.1:c.*498T>C	NP_001307548.1:n.*498T>C
NM_152871.3:c.*167T>C	NP_690610.1:n.*167T>C
NM_152872.3:c.*487T>C	NP_690611.1:n.*487T>C
NR_028033.3:n.1321T>C
NR_028034.3:n.1183T>C
NR_028035.3:n.1246T>C
NR_028036.3:n.1384T>C
NR_135313.1:n.1301T>C
NR_135314.1:n.1484T>C
NR_135315.1:n.1237T>C
XM_006717819.3:c.*167T>C	XP_006717882.1:n.*167T>C
XM_011539764.2:c.*167T>C	XP_011538066.1:n.*167T>C
XM_011539765.2:c.*167T>C	XP_011538067.1:n.*167T>C
XM_011539766.2:c.*167T>C	XP_011538068.1:n.*167T>C
XM_011539767.3:c.*167T>C	XP_011538069.1:n.*167T>C
XR_945732.3:n.1243T>C
XR_945733.2:n.1180T>C
NM_000043.6:c.*167T>C MANE Select	NP_000034.1:n.*167T>C
NM_001320619.2:c.*498T>C	NP_001307548.1:n.*498T>C
NM_152871.4:c.*167T>C	NP_690610.1:n.*167T>C
NM_152872.4:c.*487T>C	NP_690611.1:n.*487T>C
NR_028033.4:n.1082T>C
NR_028034.4:n.944T>C
NR_028035.4:n.1007T>C
NR_028036.4:n.1145T>C
NR_135313.2:n.1062T>C
NR_135314.2:n.1341T>C
NR_135315.2:n.1094T>C