Canonical Allele Identifier: CA2610079848

Gene: FAS

Linked Data

• gnomAD v4: 10-89014710-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014710G>T , CM000672.2:g.89014710G>T	GRCh38
NC_000010.10:g.90774467G>T , CM000672.1:g.90774467G>T	GRCh37
NC_000010.9:g.90764447G>T	NCBI36
NG_009089.2:g.29180G>T , LRG_134:g.29180G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1577G>T
ENST00000355740.8:c.*591G>T	ENSP00000347979.3:n.*591G>T
ENST00000357339.7:c.*260G>T	ENSP00000349896.2:n.*260G>T
ENST00000371857.8:n.2813G>T
ENST00000460510.6:c.*260G>T	ENSP00000512812.1:n.*260G>T
ENST00000466081.6:n.2917G>T
ENST00000477270.6:c.*260G>T	ENSP00000512813.1:n.*260G>T
ENST00000492756.7:c.*697G>T	ENSP00000422453.1:n.*697G>T
ENST00000494799.6:c.*260G>T	ENSP00000512834.1:n.*260G>T
ENST00000562983.3:c.*260G>T	ENSP00000512845.1:n.*260G>T
ENST00000612663.6:c.*670G>T	ENSP00000477997.3:n.*670G>T
ENST00000640140.2:n.1413G>T
ENST00000640250.2:n.767G>T
ENST00000640681.2:n.1372G>T
ENST00000696723.1:n.4901G>T
ENST00000696741.1:n.2906G>T
ENST00000696742.1:n.2633G>T
ENST00000696743.1:n.4036G>T
ENST00000696744.1:n.1307G>T
ENST00000696767.1:n.1602G>T
ENST00000696768.1:c.*591G>T	ENSP00000512859.1:n.*591G>T
ENST00000696771.1:c.*260G>T	ENSP00000512860.1:n.*260G>T
ENST00000696772.1:n.2871G>T
ENST00000696773.1:n.2610G>T
ENST00000696774.1:n.6378G>T
ENST00000696776.1:c.*260G>T	ENSP00000512861.1:n.*260G>T
ENST00000696777.1:n.2676G>T
ENST00000696778.1:n.1704G>T
ENST00000696779.1:c.*260G>T	ENSP00000512862.1:n.*260G>T
ENST00000696780.1:c.*260G>T	ENSP00000512863.1:n.*260G>T
ENST00000696781.1:c.*260G>T	ENSP00000512864.1:n.*260G>T
ENST00000696782.1:c.*670G>T	ENSP00000512865.1:n.*670G>T
ENST00000696783.1:n.3136G>T
ENST00000696992.1:n.2385G>T
ENST00000696995.1:n.4797G>T
ENST00000696996.1:n.2710G>T
ENST00000696997.1:c.*898G>T	ENSP00000513028.1:n.*898G>T
ENST00000696998.1:n.2522G>T
ENST00000696999.1:c.*260G>T	ENSP00000513029.1:n.*260G>T
ENST00000697036.1:c.*684G>T	ENSP00000513060.1:n.*684G>T
ENST00000697037.1:n.1303G>T
ENST00000697093.1:n.3504G>T
ENST00000697094.1:n.3851G>T
ENST00000697095.1:c.*2469G>T	ENSP00000513104.1:n.*2469G>T
ENST00000697096.1:n.2401G>T
ENST00000697097.1:c.*260G>T	ENSP00000513105.1:n.*260G>T
ENST00000562983.2:n.1454G>T
ENST00000690268.1:c.*260G>T	ENSP00000509810.1:n.*260G>T
ENST00000355740.7:c.*594G>T	ENSP00000347979.3:n.*594G>T
ENST00000640140.1:n.1440G>T
ENST00000640250.1:n.767G>T
ENST00000640681.1:n.1389G>T
ENST00000652046.1:c.*260G>T MANE Select	ENSP00000498466.1:n.*260G>T
ENST00000352159.8:c.*585G>T	ENSP00000345601.4:n.*585G>T
ENST00000355740.6:c.*260G>T	ENSP00000347979.2:n.*260G>T
NM_000043.4:c.*260G>T , LRG_134t1:c.*260G>T	NP_000034.1:n.*260G>T
NM_152871.2:c.*260G>T	NP_690610.1:n.*260G>T
NM_152872.2:c.*580G>T	NP_690611.1:n.*580G>T
NR_028033.2:n.1442G>T
NR_028034.2:n.1304G>T
NR_028035.2:n.1367G>T
NR_028036.2:n.1505G>T
XM_006717819.2:c.*260G>T	XP_006717882.1:n.*260G>T
XM_011539764.1:c.*260G>T	XP_011538066.1:n.*260G>T
XM_011539765.1:c.*260G>T	XP_011538067.1:n.*260G>T
XM_011539766.1:c.*260G>T	XP_011538068.1:n.*260G>T
XM_011539767.1:c.*260G>T	XP_011538069.1:n.*260G>T
NM_000043.5:c.*260G>T	NP_000034.1:n.*260G>T
NM_001320619.1:c.*591G>T	NP_001307548.1:n.*591G>T
NM_152871.3:c.*260G>T	NP_690610.1:n.*260G>T
NM_152872.3:c.*580G>T	NP_690611.1:n.*580G>T
NR_028033.3:n.1414G>T
NR_028034.3:n.1276G>T
NR_028035.3:n.1339G>T
NR_028036.3:n.1477G>T
NR_135313.1:n.1394G>T
NR_135314.1:n.1577G>T
NR_135315.1:n.1330G>T
XM_006717819.3:c.*260G>T	XP_006717882.1:n.*260G>T
XM_011539764.2:c.*260G>T	XP_011538066.1:n.*260G>T
XM_011539765.2:c.*260G>T	XP_011538067.1:n.*260G>T
XM_011539766.2:c.*260G>T	XP_011538068.1:n.*260G>T
XM_011539767.3:c.*260G>T	XP_011538069.1:n.*260G>T
XR_945732.3:n.1336G>T
XR_945733.2:n.1273G>T
NM_000043.6:c.*260G>T MANE Select	NP_000034.1:n.*260G>T
NM_001320619.2:c.*591G>T	NP_001307548.1:n.*591G>T
NM_152871.4:c.*260G>T	NP_690610.1:n.*260G>T
NM_152872.4:c.*580G>T	NP_690611.1:n.*580G>T
NR_028033.4:n.1175G>T
NR_028034.4:n.1037G>T
NR_028035.4:n.1100G>T
NR_028036.4:n.1238G>T
NR_135313.2:n.1155G>T
NR_135314.2:n.1434G>T
NR_135315.2:n.1187G>T