Canonical Allele Identifier: CA377510031

Gene: FAS

Linked Data

• gnomAD v4: 10-89014326-T-C
• MyVariant Identifiers: chr10:g.90774083T>C (hg19) ; chr10:g.89014326T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014326T>C , CM000672.2:g.89014326T>C	GRCh38
NC_000010.10:g.90774083T>C , CM000672.1:g.90774083T>C	GRCh37
NC_000010.9:g.90764063T>C	NCBI36
NG_009089.2:g.28796T>C , LRG_134:g.28796T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1193T>C
ENST00000355740.8:c.*207T>C	ENSP00000347979.3:n.*207T>C
ENST00000357339.7:c.821T>C	ENSP00000349896.2:p.Ile274Thr
ENST00000371857.8:n.2429T>C
ENST00000460510.6:c.167T>C	ENSP00000512812.1:p.Ile56Thr
ENST00000466081.6:n.2533T>C
ENST00000477270.6:c.929T>C	ENSP00000512813.1:p.Ile310Thr
ENST00000479522.6:c.*313T>C	ENSP00000424113.1:n.*313T>C
ENST00000484444.6:c.*325T>C	ENSP00000420975.1:n.*325T>C
ENST00000488877.6:c.775T>C	ENSP00000425159.1:n.775T>C
ENST00000492756.7:c.*313T>C	ENSP00000422453.1:n.*313T>C
ENST00000494799.6:c.167T>C	ENSP00000512834.1:p.Ile56Thr
ENST00000562983.3:c.167T>C	ENSP00000512845.1:p.Ile56Thr
ENST00000612663.6:c.*286T>C	ENSP00000477997.3:n.*286T>C
ENST00000640140.2:n.1029T>C
ENST00000640250.2:n.383T>C
ENST00000640681.2:n.988T>C
ENST00000696723.1:n.4517T>C
ENST00000696741.1:n.2522T>C
ENST00000696742.1:n.2249T>C
ENST00000696743.1:n.3652T>C
ENST00000696744.1:n.923T>C
ENST00000696767.1:n.1218T>C
ENST00000696768.1:c.*207T>C	ENSP00000512859.1:n.*207T>C
ENST00000696769.1:n.2573T>C
ENST00000696771.1:c.167T>C	ENSP00000512860.1:p.Ile56Thr
ENST00000696772.1:n.2487T>C
ENST00000696773.1:n.2226T>C
ENST00000696774.1:n.5994T>C
ENST00000696776.1:c.977T>C	ENSP00000512861.1:p.Ile326Thr
ENST00000696777.1:n.2292T>C
ENST00000696778.1:n.1320T>C
ENST00000696779.1:c.491T>C	ENSP00000512862.1:p.Ile164Thr
ENST00000696780.1:c.914T>C	ENSP00000512863.1:p.Ile305Thr
ENST00000696781.1:c.629T>C	ENSP00000512864.1:p.Ile210Thr
ENST00000696782.1:c.*286T>C	ENSP00000512865.1:n.*286T>C
ENST00000696783.1:n.2752T>C
ENST00000696992.1:n.2001T>C
ENST00000696995.1:n.4413T>C
ENST00000696996.1:n.2326T>C
ENST00000696997.1:c.*514T>C	ENSP00000513028.1:n.*514T>C
ENST00000696998.1:n.2138T>C
ENST00000696999.1:c.167T>C	ENSP00000513029.1:p.Ile56Thr
ENST00000697036.1:c.*300T>C	ENSP00000513060.1:n.*300T>C
ENST00000697037.1:n.919T>C
ENST00000697093.1:n.3120T>C
ENST00000697094.1:n.3467T>C
ENST00000697095.1:c.*2085T>C	ENSP00000513104.1:n.*2085T>C
ENST00000697096.1:n.2017T>C
ENST00000697097.1:c.167T>C	ENSP00000513105.1:p.Ile56Thr
ENST00000562983.2:n.1070T>C
ENST00000690268.1:c.965T>C	ENSP00000509810.1:p.Ile322Thr
ENST00000355740.7:c.*210T>C	ENSP00000347979.3:n.*210T>C
ENST00000612663.5:c.*286T>C	ENSP00000477997.3:n.*286T>C
ENST00000640140.1:n.1056T>C
ENST00000640250.1:n.383T>C
ENST00000640681.1:n.1005T>C
ENST00000652046.1:c.884T>C MANE Select	ENSP00000498466.1:p.Ile295Thr
ENST00000352159.8:c.*201T>C	ENSP00000345601.4:n.*201T>C
ENST00000355279.2:c.859T>C	ENSP00000347426.2:n.859T>C
ENST00000355740.6:c.884T>C	ENSP00000347979.2:p.Ile295Thr
ENST00000357339.6:c.821T>C	ENSP00000349896.2:p.Ile274Thr
ENST00000479522.5:c.*313T>C	ENSP00000424113.1:n.*313T>C
ENST00000484444.5:c.*325T>C	ENSP00000420975.1:n.*325T>C
ENST00000488877.5:c.*325T>C	ENSP00000425159.1:n.*325T>C
ENST00000492756.5:c.712T>C	ENSP00000422453.1:n.712T>C
ENST00000494410.5:c.*242T>C	ENSP00000423755.1:n.*242T>C
ENST00000612663.4:c.*231T>C	ENSP00000477997.2:n.*231T>C
NM_000043.4:c.884T>C , LRG_134t1:c.884T>C	NP_000034.1:p.Ile295Thr
NM_152871.2:c.821T>C	NP_690610.1:p.Ile274Thr
NM_152872.2:c.*196T>C	NP_690611.1:n.*196T>C
NR_028033.2:n.1058T>C
NR_028034.2:n.920T>C
NR_028035.2:n.983T>C
NR_028036.2:n.1121T>C
XM_006717819.2:c.965T>C	XP_006717882.1:p.Ile322Thr
XM_011539764.1:c.1046T>C	XP_011538066.1:p.Ile349Thr
XM_011539765.1:c.983T>C	XP_011538067.1:p.Ile328Thr
XM_011539766.1:c.965T>C	XP_011538068.1:p.Ile322Thr
XM_011539767.1:c.929T>C	XP_011538069.1:p.Ile310Thr
XR_945732.1:n.952T>C
XR_945733.1:n.889T>C
NM_000043.5:c.884T>C	NP_000034.1:p.Ile295Thr
NM_001320619.1:c.*207T>C	NP_001307548.1:n.*207T>C
NM_152871.3:c.821T>C	NP_690610.1:p.Ile274Thr
NM_152872.3:c.*196T>C	NP_690611.1:n.*196T>C
NR_028033.3:n.1030T>C
NR_028034.3:n.892T>C
NR_028035.3:n.955T>C
NR_028036.3:n.1093T>C
NR_135313.1:n.1010T>C
NR_135314.1:n.1193T>C
NR_135315.1:n.946T>C
XM_006717819.3:c.965T>C	XP_006717882.1:p.Ile322Thr
XM_011539764.2:c.1046T>C	XP_011538066.1:p.Ile349Thr
XM_011539765.2:c.983T>C	XP_011538067.1:p.Ile328Thr
XM_011539766.2:c.965T>C	XP_011538068.1:p.Ile322Thr
XM_011539767.3:c.929T>C	XP_011538069.1:p.Ile310Thr
XR_945732.3:n.952T>C
XR_945733.2:n.889T>C
NM_000043.6:c.884T>C MANE Select	NP_000034.1:p.Ile295Thr
NM_001320619.2:c.*207T>C	NP_001307548.1:n.*207T>C
NM_152871.4:c.821T>C	NP_690610.1:p.Ile274Thr
NM_152872.4:c.*196T>C	NP_690611.1:n.*196T>C
NR_028033.4:n.791T>C
NR_028034.4:n.653T>C
NR_028035.4:n.716T>C
NR_028036.4:n.854T>C
NR_135313.2:n.771T>C
NR_135314.2:n.1050T>C
NR_135315.2:n.803T>C