Canonical Allele Identifier: CA2610079798

Gene: FAS

Linked Data

• gnomAD v4: 10-89014663-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014663G>T , CM000672.2:g.89014663G>T	GRCh38
NC_000010.10:g.90774420G>T , CM000672.1:g.90774420G>T	GRCh37
NC_000010.9:g.90764400G>T	NCBI36
NG_009089.2:g.29133G>T , LRG_134:g.29133G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1530G>T
ENST00000355740.8:c.*544G>T	ENSP00000347979.3:n.*544G>T
ENST00000357339.7:c.*213G>T	ENSP00000349896.2:n.*213G>T
ENST00000371857.8:n.2766G>T
ENST00000460510.6:c.*213G>T	ENSP00000512812.1:n.*213G>T
ENST00000466081.6:n.2870G>T
ENST00000477270.6:c.*213G>T	ENSP00000512813.1:n.*213G>T
ENST00000492756.7:c.*650G>T	ENSP00000422453.1:n.*650G>T
ENST00000494799.6:c.*213G>T	ENSP00000512834.1:n.*213G>T
ENST00000562983.3:c.*213G>T	ENSP00000512845.1:n.*213G>T
ENST00000612663.6:c.*623G>T	ENSP00000477997.3:n.*623G>T
ENST00000640140.2:n.1366G>T
ENST00000640250.2:n.720G>T
ENST00000640681.2:n.1325G>T
ENST00000696723.1:n.4854G>T
ENST00000696741.1:n.2859G>T
ENST00000696742.1:n.2586G>T
ENST00000696743.1:n.3989G>T
ENST00000696744.1:n.1260G>T
ENST00000696767.1:n.1555G>T
ENST00000696768.1:c.*544G>T	ENSP00000512859.1:n.*544G>T
ENST00000696771.1:c.*213G>T	ENSP00000512860.1:n.*213G>T
ENST00000696772.1:n.2824G>T
ENST00000696773.1:n.2563G>T
ENST00000696774.1:n.6331G>T
ENST00000696776.1:c.*213G>T	ENSP00000512861.1:n.*213G>T
ENST00000696777.1:n.2629G>T
ENST00000696778.1:n.1657G>T
ENST00000696779.1:c.*213G>T	ENSP00000512862.1:n.*213G>T
ENST00000696780.1:c.*213G>T	ENSP00000512863.1:n.*213G>T
ENST00000696781.1:c.*213G>T	ENSP00000512864.1:n.*213G>T
ENST00000696782.1:c.*623G>T	ENSP00000512865.1:n.*623G>T
ENST00000696783.1:n.3089G>T
ENST00000696992.1:n.2338G>T
ENST00000696995.1:n.4750G>T
ENST00000696996.1:n.2663G>T
ENST00000696997.1:c.*851G>T	ENSP00000513028.1:n.*851G>T
ENST00000696998.1:n.2475G>T
ENST00000696999.1:c.*213G>T	ENSP00000513029.1:n.*213G>T
ENST00000697036.1:c.*637G>T	ENSP00000513060.1:n.*637G>T
ENST00000697037.1:n.1256G>T
ENST00000697093.1:n.3457G>T
ENST00000697094.1:n.3804G>T
ENST00000697095.1:c.*2422G>T	ENSP00000513104.1:n.*2422G>T
ENST00000697096.1:n.2354G>T
ENST00000697097.1:c.*213G>T	ENSP00000513105.1:n.*213G>T
ENST00000562983.2:n.1407G>T
ENST00000690268.1:c.*213G>T	ENSP00000509810.1:n.*213G>T
ENST00000355740.7:c.*547G>T	ENSP00000347979.3:n.*547G>T
ENST00000640140.1:n.1393G>T
ENST00000640250.1:n.720G>T
ENST00000640681.1:n.1342G>T
ENST00000652046.1:c.*213G>T MANE Select	ENSP00000498466.1:n.*213G>T
ENST00000352159.8:c.*538G>T	ENSP00000345601.4:n.*538G>T
ENST00000355740.6:c.*213G>T	ENSP00000347979.2:n.*213G>T
NM_000043.4:c.*213G>T , LRG_134t1:c.*213G>T	NP_000034.1:n.*213G>T
NM_152871.2:c.*213G>T	NP_690610.1:n.*213G>T
NM_152872.2:c.*533G>T	NP_690611.1:n.*533G>T
NR_028033.2:n.1395G>T
NR_028034.2:n.1257G>T
NR_028035.2:n.1320G>T
NR_028036.2:n.1458G>T
XM_006717819.2:c.*213G>T	XP_006717882.1:n.*213G>T
XM_011539764.1:c.*213G>T	XP_011538066.1:n.*213G>T
XM_011539765.1:c.*213G>T	XP_011538067.1:n.*213G>T
XM_011539766.1:c.*213G>T	XP_011538068.1:n.*213G>T
XM_011539767.1:c.*213G>T	XP_011538069.1:n.*213G>T
NM_000043.5:c.*213G>T	NP_000034.1:n.*213G>T
NM_001320619.1:c.*544G>T	NP_001307548.1:n.*544G>T
NM_152871.3:c.*213G>T	NP_690610.1:n.*213G>T
NM_152872.3:c.*533G>T	NP_690611.1:n.*533G>T
NR_028033.3:n.1367G>T
NR_028034.3:n.1229G>T
NR_028035.3:n.1292G>T
NR_028036.3:n.1430G>T
NR_135313.1:n.1347G>T
NR_135314.1:n.1530G>T
NR_135315.1:n.1283G>T
XM_006717819.3:c.*213G>T	XP_006717882.1:n.*213G>T
XM_011539764.2:c.*213G>T	XP_011538066.1:n.*213G>T
XM_011539765.2:c.*213G>T	XP_011538067.1:n.*213G>T
XM_011539766.2:c.*213G>T	XP_011538068.1:n.*213G>T
XM_011539767.3:c.*213G>T	XP_011538069.1:n.*213G>T
XR_945732.3:n.1289G>T
XR_945733.2:n.1226G>T
NM_000043.6:c.*213G>T MANE Select	NP_000034.1:n.*213G>T
NM_001320619.2:c.*544G>T	NP_001307548.1:n.*544G>T
NM_152871.4:c.*213G>T	NP_690610.1:n.*213G>T
NM_152872.4:c.*533G>T	NP_690611.1:n.*533G>T
NR_028033.4:n.1128G>T
NR_028034.4:n.990G>T
NR_028035.4:n.1053G>T
NR_028036.4:n.1191G>T
NR_135313.2:n.1108G>T
NR_135314.2:n.1387G>T
NR_135315.2:n.1140G>T