Canonical Allele Identifier: CA1926639509

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014614G= , CM000672.2:g.89014614G=	GRCh38
NC_000010.10:g.90774371G= , CM000672.1:g.90774371G=	GRCh37
NC_000010.9:g.90764351G=	NCBI36
NG_009089.2:g.29084G= , LRG_134:g.29084G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1481G=
ENST00000355740.8:c.*495G=	ENSP00000347979.3:n.*495G=
ENST00000357339.7:c.*164G=	ENSP00000349896.2:n.*164G=
ENST00000371857.8:n.2717G=
ENST00000460510.6:c.*164G=	ENSP00000512812.1:n.*164G=
ENST00000466081.6:n.2821G=
ENST00000477270.6:c.*164G=	ENSP00000512813.1:n.*164G=
ENST00000488877.6:c.1063G=	ENSP00000425159.1:n.1063G=
ENST00000492756.7:c.*601G=	ENSP00000422453.1:n.*601G=
ENST00000494799.6:c.*164G=	ENSP00000512834.1:n.*164G=
ENST00000562983.3:c.*164G=	ENSP00000512845.1:n.*164G=
ENST00000612663.6:c.*574G=	ENSP00000477997.3:n.*574G=
ENST00000640140.2:n.1317G=
ENST00000640250.2:n.671G=
ENST00000640681.2:n.1276G=
ENST00000696723.1:n.4805G=
ENST00000696741.1:n.2810G=
ENST00000696742.1:n.2537G=
ENST00000696743.1:n.3940G=
ENST00000696744.1:n.1211G=
ENST00000696767.1:n.1506G=
ENST00000696768.1:c.*495G=	ENSP00000512859.1:n.*495G=
ENST00000696771.1:c.*164G=	ENSP00000512860.1:n.*164G=
ENST00000696772.1:n.2775G=
ENST00000696773.1:n.2514G=
ENST00000696774.1:n.6282G=
ENST00000696776.1:c.*164G=	ENSP00000512861.1:n.*164G=
ENST00000696777.1:n.2580G=
ENST00000696778.1:n.1608G=
ENST00000696779.1:c.*164G=	ENSP00000512862.1:n.*164G=
ENST00000696780.1:c.*164G=	ENSP00000512863.1:n.*164G=
ENST00000696781.1:c.*164G=	ENSP00000512864.1:n.*164G=
ENST00000696782.1:c.*574G=	ENSP00000512865.1:n.*574G=
ENST00000696783.1:n.3040G=
ENST00000696992.1:n.2289G=
ENST00000696995.1:n.4701G=
ENST00000696996.1:n.2614G=
ENST00000696997.1:c.*802G=	ENSP00000513028.1:n.*802G=
ENST00000696998.1:n.2426G=
ENST00000696999.1:c.*164G=	ENSP00000513029.1:n.*164G=
ENST00000697036.1:c.*588G=	ENSP00000513060.1:n.*588G=
ENST00000697037.1:n.1207G=
ENST00000697093.1:n.3408G=
ENST00000697094.1:n.3755G=
ENST00000697095.1:c.*2373G=	ENSP00000513104.1:n.*2373G=
ENST00000697096.1:n.2305G=
ENST00000697097.1:c.*164G=	ENSP00000513105.1:n.*164G=
ENST00000562983.2:n.1358G=
ENST00000690268.1:c.*164G=	ENSP00000509810.1:n.*164G=
ENST00000355740.7:c.*498G=	ENSP00000347979.3:n.*498G=
ENST00000640140.1:n.1344G=
ENST00000640250.1:n.671G=
ENST00000640681.1:n.1293G=
ENST00000652046.1:c.*164G= MANE Select	ENSP00000498466.1:n.*164G=
ENST00000352159.8:c.*489G=	ENSP00000345601.4:n.*489G=
ENST00000355740.6:c.*164G=	ENSP00000347979.2:n.*164G=
ENST00000484444.5:c.*613G=	ENSP00000420975.1:n.*613G=
NM_000043.4:c.*164G= , LRG_134t1:c.*164G=	NP_000034.1:n.*164G=
NM_152871.2:c.*164G=	NP_690610.1:n.*164G=
NM_152872.2:c.*484G=	NP_690611.1:n.*484G=
NR_028033.2:n.1346G=
NR_028034.2:n.1208G=
NR_028035.2:n.1271G=
NR_028036.2:n.1409G=
XM_006717819.2:c.*164G=	XP_006717882.1:n.*164G=
XM_011539764.1:c.*164G=	XP_011538066.1:n.*164G=
XM_011539765.1:c.*164G=	XP_011538067.1:n.*164G=
XM_011539766.1:c.*164G=	XP_011538068.1:n.*164G=
XM_011539767.1:c.*164G=	XP_011538069.1:n.*164G=
NM_000043.5:c.*164G=	NP_000034.1:n.*164G=
NM_001320619.1:c.*495G=	NP_001307548.1:n.*495G=
NM_152871.3:c.*164G=	NP_690610.1:n.*164G=
NM_152872.3:c.*484G=	NP_690611.1:n.*484G=
NR_028033.3:n.1318G=
NR_028034.3:n.1180G=
NR_028035.3:n.1243G=
NR_028036.3:n.1381G=
NR_135313.1:n.1298G=
NR_135314.1:n.1481G=
NR_135315.1:n.1234G=
XM_006717819.3:c.*164G=	XP_006717882.1:n.*164G=
XM_011539764.2:c.*164G=	XP_011538066.1:n.*164G=
XM_011539765.2:c.*164G=	XP_011538067.1:n.*164G=
XM_011539766.2:c.*164G=	XP_011538068.1:n.*164G=
XM_011539767.3:c.*164G=	XP_011538069.1:n.*164G=
XR_945732.3:n.1240G=
XR_945733.2:n.1177G=
NM_000043.6:c.*164G= MANE Select	NP_000034.1:n.*164G=
NM_001320619.2:c.*495G=	NP_001307548.1:n.*495G=
NM_152871.4:c.*164G=	NP_690610.1:n.*164G=
NM_152872.4:c.*484G=	NP_690611.1:n.*484G=
NR_028033.4:n.1079G=
NR_028034.4:n.941G=
NR_028035.4:n.1004G=
NR_028036.4:n.1142G=
NR_135313.2:n.1059G=
NR_135314.2:n.1338G=
NR_135315.2:n.1091G=