Canonical Allele Identifier: CA2610079819

Gene: FAS

Linked Data

• gnomAD v4: 10-89014679-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014679G>T , CM000672.2:g.89014679G>T	GRCh38
NC_000010.10:g.90774436G>T , CM000672.1:g.90774436G>T	GRCh37
NC_000010.9:g.90764416G>T	NCBI36
NG_009089.2:g.29149G>T , LRG_134:g.29149G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1546G>T
ENST00000355740.8:c.*560G>T	ENSP00000347979.3:n.*560G>T
ENST00000357339.7:c.*229G>T	ENSP00000349896.2:n.*229G>T
ENST00000371857.8:n.2782G>T
ENST00000460510.6:c.*229G>T	ENSP00000512812.1:n.*229G>T
ENST00000466081.6:n.2886G>T
ENST00000477270.6:c.*229G>T	ENSP00000512813.1:n.*229G>T
ENST00000492756.7:c.*666G>T	ENSP00000422453.1:n.*666G>T
ENST00000494799.6:c.*229G>T	ENSP00000512834.1:n.*229G>T
ENST00000562983.3:c.*229G>T	ENSP00000512845.1:n.*229G>T
ENST00000612663.6:c.*639G>T	ENSP00000477997.3:n.*639G>T
ENST00000640140.2:n.1382G>T
ENST00000640250.2:n.736G>T
ENST00000640681.2:n.1341G>T
ENST00000696723.1:n.4870G>T
ENST00000696741.1:n.2875G>T
ENST00000696742.1:n.2602G>T
ENST00000696743.1:n.4005G>T
ENST00000696744.1:n.1276G>T
ENST00000696767.1:n.1571G>T
ENST00000696768.1:c.*560G>T	ENSP00000512859.1:n.*560G>T
ENST00000696771.1:c.*229G>T	ENSP00000512860.1:n.*229G>T
ENST00000696772.1:n.2840G>T
ENST00000696773.1:n.2579G>T
ENST00000696774.1:n.6347G>T
ENST00000696776.1:c.*229G>T	ENSP00000512861.1:n.*229G>T
ENST00000696777.1:n.2645G>T
ENST00000696778.1:n.1673G>T
ENST00000696779.1:c.*229G>T	ENSP00000512862.1:n.*229G>T
ENST00000696780.1:c.*229G>T	ENSP00000512863.1:n.*229G>T
ENST00000696781.1:c.*229G>T	ENSP00000512864.1:n.*229G>T
ENST00000696782.1:c.*639G>T	ENSP00000512865.1:n.*639G>T
ENST00000696783.1:n.3105G>T
ENST00000696992.1:n.2354G>T
ENST00000696995.1:n.4766G>T
ENST00000696996.1:n.2679G>T
ENST00000696997.1:c.*867G>T	ENSP00000513028.1:n.*867G>T
ENST00000696998.1:n.2491G>T
ENST00000696999.1:c.*229G>T	ENSP00000513029.1:n.*229G>T
ENST00000697036.1:c.*653G>T	ENSP00000513060.1:n.*653G>T
ENST00000697037.1:n.1272G>T
ENST00000697093.1:n.3473G>T
ENST00000697094.1:n.3820G>T
ENST00000697095.1:c.*2438G>T	ENSP00000513104.1:n.*2438G>T
ENST00000697096.1:n.2370G>T
ENST00000697097.1:c.*229G>T	ENSP00000513105.1:n.*229G>T
ENST00000562983.2:n.1423G>T
ENST00000690268.1:c.*229G>T	ENSP00000509810.1:n.*229G>T
ENST00000355740.7:c.*563G>T	ENSP00000347979.3:n.*563G>T
ENST00000640140.1:n.1409G>T
ENST00000640250.1:n.736G>T
ENST00000640681.1:n.1358G>T
ENST00000652046.1:c.*229G>T MANE Select	ENSP00000498466.1:n.*229G>T
ENST00000352159.8:c.*554G>T	ENSP00000345601.4:n.*554G>T
ENST00000355740.6:c.*229G>T	ENSP00000347979.2:n.*229G>T
NM_000043.4:c.*229G>T , LRG_134t1:c.*229G>T	NP_000034.1:n.*229G>T
NM_152871.2:c.*229G>T	NP_690610.1:n.*229G>T
NM_152872.2:c.*549G>T	NP_690611.1:n.*549G>T
NR_028033.2:n.1411G>T
NR_028034.2:n.1273G>T
NR_028035.2:n.1336G>T
NR_028036.2:n.1474G>T
XM_006717819.2:c.*229G>T	XP_006717882.1:n.*229G>T
XM_011539764.1:c.*229G>T	XP_011538066.1:n.*229G>T
XM_011539765.1:c.*229G>T	XP_011538067.1:n.*229G>T
XM_011539766.1:c.*229G>T	XP_011538068.1:n.*229G>T
XM_011539767.1:c.*229G>T	XP_011538069.1:n.*229G>T
NM_000043.5:c.*229G>T	NP_000034.1:n.*229G>T
NM_001320619.1:c.*560G>T	NP_001307548.1:n.*560G>T
NM_152871.3:c.*229G>T	NP_690610.1:n.*229G>T
NM_152872.3:c.*549G>T	NP_690611.1:n.*549G>T
NR_028033.3:n.1383G>T
NR_028034.3:n.1245G>T
NR_028035.3:n.1308G>T
NR_028036.3:n.1446G>T
NR_135313.1:n.1363G>T
NR_135314.1:n.1546G>T
NR_135315.1:n.1299G>T
XM_006717819.3:c.*229G>T	XP_006717882.1:n.*229G>T
XM_011539764.2:c.*229G>T	XP_011538066.1:n.*229G>T
XM_011539765.2:c.*229G>T	XP_011538067.1:n.*229G>T
XM_011539766.2:c.*229G>T	XP_011538068.1:n.*229G>T
XM_011539767.3:c.*229G>T	XP_011538069.1:n.*229G>T
XR_945732.3:n.1305G>T
XR_945733.2:n.1242G>T
NM_000043.6:c.*229G>T MANE Select	NP_000034.1:n.*229G>T
NM_001320619.2:c.*560G>T	NP_001307548.1:n.*560G>T
NM_152871.4:c.*229G>T	NP_690610.1:n.*229G>T
NM_152872.4:c.*549G>T	NP_690611.1:n.*549G>T
NR_028033.4:n.1144G>T
NR_028034.4:n.1006G>T
NR_028035.4:n.1069G>T
NR_028036.4:n.1207G>T
NR_135313.2:n.1124G>T
NR_135314.2:n.1403G>T
NR_135315.2:n.1156G>T