Canonical Allele Identifier: CA2610079764

Gene: FAS

Linked Data

• gnomAD v4: 10-89014627-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014627T>C , CM000672.2:g.89014627T>C	GRCh38
NC_000010.10:g.90774384T>C , CM000672.1:g.90774384T>C	GRCh37
NC_000010.9:g.90764364T>C	NCBI36
NG_009089.2:g.29097T>C , LRG_134:g.29097T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1494T>C
ENST00000355740.8:c.*508T>C	ENSP00000347979.3:n.*508T>C
ENST00000357339.7:c.*177T>C	ENSP00000349896.2:n.*177T>C
ENST00000371857.8:n.2730T>C
ENST00000460510.6:c.*177T>C	ENSP00000512812.1:n.*177T>C
ENST00000466081.6:n.2834T>C
ENST00000477270.6:c.*177T>C	ENSP00000512813.1:n.*177T>C
ENST00000488877.6:c.1076T>C	ENSP00000425159.1:n.1076T>C
ENST00000492756.7:c.*614T>C	ENSP00000422453.1:n.*614T>C
ENST00000494799.6:c.*177T>C	ENSP00000512834.1:n.*177T>C
ENST00000562983.3:c.*177T>C	ENSP00000512845.1:n.*177T>C
ENST00000612663.6:c.*587T>C	ENSP00000477997.3:n.*587T>C
ENST00000640140.2:n.1330T>C
ENST00000640250.2:n.684T>C
ENST00000640681.2:n.1289T>C
ENST00000696723.1:n.4818T>C
ENST00000696741.1:n.2823T>C
ENST00000696742.1:n.2550T>C
ENST00000696743.1:n.3953T>C
ENST00000696744.1:n.1224T>C
ENST00000696767.1:n.1519T>C
ENST00000696768.1:c.*508T>C	ENSP00000512859.1:n.*508T>C
ENST00000696771.1:c.*177T>C	ENSP00000512860.1:n.*177T>C
ENST00000696772.1:n.2788T>C
ENST00000696773.1:n.2527T>C
ENST00000696774.1:n.6295T>C
ENST00000696776.1:c.*177T>C	ENSP00000512861.1:n.*177T>C
ENST00000696777.1:n.2593T>C
ENST00000696778.1:n.1621T>C
ENST00000696779.1:c.*177T>C	ENSP00000512862.1:n.*177T>C
ENST00000696780.1:c.*177T>C	ENSP00000512863.1:n.*177T>C
ENST00000696781.1:c.*177T>C	ENSP00000512864.1:n.*177T>C
ENST00000696782.1:c.*587T>C	ENSP00000512865.1:n.*587T>C
ENST00000696783.1:n.3053T>C
ENST00000696992.1:n.2302T>C
ENST00000696995.1:n.4714T>C
ENST00000696996.1:n.2627T>C
ENST00000696997.1:c.*815T>C	ENSP00000513028.1:n.*815T>C
ENST00000696998.1:n.2439T>C
ENST00000696999.1:c.*177T>C	ENSP00000513029.1:n.*177T>C
ENST00000697036.1:c.*601T>C	ENSP00000513060.1:n.*601T>C
ENST00000697037.1:n.1220T>C
ENST00000697093.1:n.3421T>C
ENST00000697094.1:n.3768T>C
ENST00000697095.1:c.*2386T>C	ENSP00000513104.1:n.*2386T>C
ENST00000697096.1:n.2318T>C
ENST00000697097.1:c.*177T>C	ENSP00000513105.1:n.*177T>C
ENST00000562983.2:n.1371T>C
ENST00000690268.1:c.*177T>C	ENSP00000509810.1:n.*177T>C
ENST00000355740.7:c.*511T>C	ENSP00000347979.3:n.*511T>C
ENST00000640140.1:n.1357T>C
ENST00000640250.1:n.684T>C
ENST00000640681.1:n.1306T>C
ENST00000652046.1:c.*177T>C MANE Select	ENSP00000498466.1:n.*177T>C
ENST00000352159.8:c.*502T>C	ENSP00000345601.4:n.*502T>C
ENST00000355740.6:c.*177T>C	ENSP00000347979.2:n.*177T>C
NM_000043.4:c.*177T>C , LRG_134t1:c.*177T>C	NP_000034.1:n.*177T>C
NM_152871.2:c.*177T>C	NP_690610.1:n.*177T>C
NM_152872.2:c.*497T>C	NP_690611.1:n.*497T>C
NR_028033.2:n.1359T>C
NR_028034.2:n.1221T>C
NR_028035.2:n.1284T>C
NR_028036.2:n.1422T>C
XM_006717819.2:c.*177T>C	XP_006717882.1:n.*177T>C
XM_011539764.1:c.*177T>C	XP_011538066.1:n.*177T>C
XM_011539765.1:c.*177T>C	XP_011538067.1:n.*177T>C
XM_011539766.1:c.*177T>C	XP_011538068.1:n.*177T>C
XM_011539767.1:c.*177T>C	XP_011538069.1:n.*177T>C
NM_000043.5:c.*177T>C	NP_000034.1:n.*177T>C
NM_001320619.1:c.*508T>C	NP_001307548.1:n.*508T>C
NM_152871.3:c.*177T>C	NP_690610.1:n.*177T>C
NM_152872.3:c.*497T>C	NP_690611.1:n.*497T>C
NR_028033.3:n.1331T>C
NR_028034.3:n.1193T>C
NR_028035.3:n.1256T>C
NR_028036.3:n.1394T>C
NR_135313.1:n.1311T>C
NR_135314.1:n.1494T>C
NR_135315.1:n.1247T>C
XM_006717819.3:c.*177T>C	XP_006717882.1:n.*177T>C
XM_011539764.2:c.*177T>C	XP_011538066.1:n.*177T>C
XM_011539765.2:c.*177T>C	XP_011538067.1:n.*177T>C
XM_011539766.2:c.*177T>C	XP_011538068.1:n.*177T>C
XM_011539767.3:c.*177T>C	XP_011538069.1:n.*177T>C
XR_945732.3:n.1253T>C
XR_945733.2:n.1190T>C
NM_000043.6:c.*177T>C MANE Select	NP_000034.1:n.*177T>C
NM_001320619.2:c.*508T>C	NP_001307548.1:n.*508T>C
NM_152871.4:c.*177T>C	NP_690610.1:n.*177T>C
NM_152872.4:c.*497T>C	NP_690611.1:n.*497T>C
NR_028033.4:n.1092T>C
NR_028034.4:n.954T>C
NR_028035.4:n.1017T>C
NR_028036.4:n.1155T>C
NR_135313.2:n.1072T>C
NR_135314.2:n.1351T>C
NR_135315.2:n.1104T>C