Canonical Allele Identifier: CA2610079674

Gene: FAS

Linked Data

• gnomAD v4: 10-89014525-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014525T>C , CM000672.2:g.89014525T>C	GRCh38
NC_000010.10:g.90774282T>C , CM000672.1:g.90774282T>C	GRCh37
NC_000010.9:g.90764262T>C	NCBI36
NG_009089.2:g.28995T>C , LRG_134:g.28995T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1392T>C
ENST00000355740.8:c.*406T>C	ENSP00000347979.3:n.*406T>C
ENST00000357339.7:c.*75T>C	ENSP00000349896.2:n.*75T>C
ENST00000371857.8:n.2628T>C
ENST00000460510.6:c.*75T>C	ENSP00000512812.1:n.*75T>C
ENST00000466081.6:n.2732T>C
ENST00000477270.6:c.*75T>C	ENSP00000512813.1:n.*75T>C
ENST00000479522.6:c.*512T>C	ENSP00000424113.1:n.*512T>C
ENST00000484444.6:c.*524T>C	ENSP00000420975.1:n.*524T>C
ENST00000488877.6:c.974T>C	ENSP00000425159.1:n.974T>C
ENST00000492756.7:c.*512T>C	ENSP00000422453.1:n.*512T>C
ENST00000494799.6:c.*75T>C	ENSP00000512834.1:n.*75T>C
ENST00000562983.3:c.*75T>C	ENSP00000512845.1:n.*75T>C
ENST00000612663.6:c.*485T>C	ENSP00000477997.3:n.*485T>C
ENST00000640140.2:n.1228T>C
ENST00000640250.2:n.582T>C
ENST00000640681.2:n.1187T>C
ENST00000696723.1:n.4716T>C
ENST00000696741.1:n.2721T>C
ENST00000696742.1:n.2448T>C
ENST00000696743.1:n.3851T>C
ENST00000696744.1:n.1122T>C
ENST00000696767.1:n.1417T>C
ENST00000696768.1:c.*406T>C	ENSP00000512859.1:n.*406T>C
ENST00000696769.1:n.2772T>C
ENST00000696771.1:c.*75T>C	ENSP00000512860.1:n.*75T>C
ENST00000696772.1:n.2686T>C
ENST00000696773.1:n.2425T>C
ENST00000696774.1:n.6193T>C
ENST00000696776.1:c.*75T>C	ENSP00000512861.1:n.*75T>C
ENST00000696777.1:n.2491T>C
ENST00000696778.1:n.1519T>C
ENST00000696779.1:c.*75T>C	ENSP00000512862.1:n.*75T>C
ENST00000696780.1:c.*75T>C	ENSP00000512863.1:n.*75T>C
ENST00000696781.1:c.*75T>C	ENSP00000512864.1:n.*75T>C
ENST00000696782.1:c.*485T>C	ENSP00000512865.1:n.*485T>C
ENST00000696783.1:n.2951T>C
ENST00000696992.1:n.2200T>C
ENST00000696995.1:n.4612T>C
ENST00000696996.1:n.2525T>C
ENST00000696997.1:c.*713T>C	ENSP00000513028.1:n.*713T>C
ENST00000696998.1:n.2337T>C
ENST00000696999.1:c.*75T>C	ENSP00000513029.1:n.*75T>C
ENST00000697036.1:c.*499T>C	ENSP00000513060.1:n.*499T>C
ENST00000697037.1:n.1118T>C
ENST00000697093.1:n.3319T>C
ENST00000697094.1:n.3666T>C
ENST00000697095.1:c.*2284T>C	ENSP00000513104.1:n.*2284T>C
ENST00000697096.1:n.2216T>C
ENST00000697097.1:c.*75T>C	ENSP00000513105.1:n.*75T>C
ENST00000562983.2:n.1269T>C
ENST00000690268.1:c.*75T>C	ENSP00000509810.1:n.*75T>C
ENST00000355740.7:c.*409T>C	ENSP00000347979.3:n.*409T>C
ENST00000640140.1:n.1255T>C
ENST00000640250.1:n.582T>C
ENST00000640681.1:n.1204T>C
ENST00000652046.1:c.*75T>C MANE Select	ENSP00000498466.1:n.*75T>C
ENST00000352159.8:c.*400T>C	ENSP00000345601.4:n.*400T>C
ENST00000355740.6:c.*75T>C	ENSP00000347979.2:n.*75T>C
ENST00000479522.5:c.*512T>C	ENSP00000424113.1:n.*512T>C
ENST00000484444.5:c.*524T>C	ENSP00000420975.1:n.*524T>C
ENST00000494410.5:c.*441T>C	ENSP00000423755.1:n.*441T>C
NM_000043.4:c.*75T>C , LRG_134t1:c.*75T>C	NP_000034.1:n.*75T>C
NM_152871.2:c.*75T>C	NP_690610.1:n.*75T>C
NM_152872.2:c.*395T>C	NP_690611.1:n.*395T>C
NR_028033.2:n.1257T>C
NR_028034.2:n.1119T>C
NR_028035.2:n.1182T>C
NR_028036.2:n.1320T>C
XM_006717819.2:c.*75T>C	XP_006717882.1:n.*75T>C
XM_011539764.1:c.*75T>C	XP_011538066.1:n.*75T>C
XM_011539765.1:c.*75T>C	XP_011538067.1:n.*75T>C
XM_011539766.1:c.*75T>C	XP_011538068.1:n.*75T>C
XM_011539767.1:c.*75T>C	XP_011538069.1:n.*75T>C
NM_000043.5:c.*75T>C	NP_000034.1:n.*75T>C
NM_001320619.1:c.*406T>C	NP_001307548.1:n.*406T>C
NM_152871.3:c.*75T>C	NP_690610.1:n.*75T>C
NM_152872.3:c.*395T>C	NP_690611.1:n.*395T>C
NR_028033.3:n.1229T>C
NR_028034.3:n.1091T>C
NR_028035.3:n.1154T>C
NR_028036.3:n.1292T>C
NR_135313.1:n.1209T>C
NR_135314.1:n.1392T>C
NR_135315.1:n.1145T>C
XM_006717819.3:c.*75T>C	XP_006717882.1:n.*75T>C
XM_011539764.2:c.*75T>C	XP_011538066.1:n.*75T>C
XM_011539765.2:c.*75T>C	XP_011538067.1:n.*75T>C
XM_011539766.2:c.*75T>C	XP_011538068.1:n.*75T>C
XM_011539767.3:c.*75T>C	XP_011538069.1:n.*75T>C
XR_945732.3:n.1151T>C
XR_945733.2:n.1088T>C
NM_000043.6:c.*75T>C MANE Select	NP_000034.1:n.*75T>C
NM_001320619.2:c.*406T>C	NP_001307548.1:n.*406T>C
NM_152871.4:c.*75T>C	NP_690610.1:n.*75T>C
NM_152872.4:c.*395T>C	NP_690611.1:n.*395T>C
NR_028033.4:n.990T>C
NR_028034.4:n.852T>C
NR_028035.4:n.915T>C
NR_028036.4:n.1053T>C
NR_135313.2:n.970T>C
NR_135314.2:n.1249T>C
NR_135315.2:n.1002T>C