Canonical Allele Identifier: CA2610079716

Gene: FAS

Linked Data

• gnomAD v4: 10-89014568-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014568G>C , CM000672.2:g.89014568G>C	GRCh38
NC_000010.10:g.90774325G>C , CM000672.1:g.90774325G>C	GRCh37
NC_000010.9:g.90764305G>C	NCBI36
NG_009089.2:g.29038G>C , LRG_134:g.29038G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1435G>C
ENST00000355740.8:c.*449G>C	ENSP00000347979.3:n.*449G>C
ENST00000357339.7:c.*118G>C	ENSP00000349896.2:n.*118G>C
ENST00000371857.8:n.2671G>C
ENST00000460510.6:c.*118G>C	ENSP00000512812.1:n.*118G>C
ENST00000466081.6:n.2775G>C
ENST00000477270.6:c.*118G>C	ENSP00000512813.1:n.*118G>C
ENST00000479522.6:c.*555G>C	ENSP00000424113.1:n.*555G>C
ENST00000484444.6:c.*567G>C	ENSP00000420975.1:n.*567G>C
ENST00000488877.6:c.1017G>C	ENSP00000425159.1:n.1017G>C
ENST00000492756.7:c.*555G>C	ENSP00000422453.1:n.*555G>C
ENST00000494799.6:c.*118G>C	ENSP00000512834.1:n.*118G>C
ENST00000562983.3:c.*118G>C	ENSP00000512845.1:n.*118G>C
ENST00000612663.6:c.*528G>C	ENSP00000477997.3:n.*528G>C
ENST00000640140.2:n.1271G>C
ENST00000640250.2:n.625G>C
ENST00000640681.2:n.1230G>C
ENST00000696723.1:n.4759G>C
ENST00000696741.1:n.2764G>C
ENST00000696742.1:n.2491G>C
ENST00000696743.1:n.3894G>C
ENST00000696744.1:n.1165G>C
ENST00000696767.1:n.1460G>C
ENST00000696768.1:c.*449G>C	ENSP00000512859.1:n.*449G>C
ENST00000696771.1:c.*118G>C	ENSP00000512860.1:n.*118G>C
ENST00000696772.1:n.2729G>C
ENST00000696773.1:n.2468G>C
ENST00000696774.1:n.6236G>C
ENST00000696776.1:c.*118G>C	ENSP00000512861.1:n.*118G>C
ENST00000696777.1:n.2534G>C
ENST00000696778.1:n.1562G>C
ENST00000696779.1:c.*118G>C	ENSP00000512862.1:n.*118G>C
ENST00000696780.1:c.*118G>C	ENSP00000512863.1:n.*118G>C
ENST00000696781.1:c.*118G>C	ENSP00000512864.1:n.*118G>C
ENST00000696782.1:c.*528G>C	ENSP00000512865.1:n.*528G>C
ENST00000696783.1:n.2994G>C
ENST00000696992.1:n.2243G>C
ENST00000696995.1:n.4655G>C
ENST00000696996.1:n.2568G>C
ENST00000696997.1:c.*756G>C	ENSP00000513028.1:n.*756G>C
ENST00000696998.1:n.2380G>C
ENST00000696999.1:c.*118G>C	ENSP00000513029.1:n.*118G>C
ENST00000697036.1:c.*542G>C	ENSP00000513060.1:n.*542G>C
ENST00000697037.1:n.1161G>C
ENST00000697093.1:n.3362G>C
ENST00000697094.1:n.3709G>C
ENST00000697095.1:c.*2327G>C	ENSP00000513104.1:n.*2327G>C
ENST00000697096.1:n.2259G>C
ENST00000697097.1:c.*118G>C	ENSP00000513105.1:n.*118G>C
ENST00000562983.2:n.1312G>C
ENST00000690268.1:c.*118G>C	ENSP00000509810.1:n.*118G>C
ENST00000355740.7:c.*452G>C	ENSP00000347979.3:n.*452G>C
ENST00000640140.1:n.1298G>C
ENST00000640250.1:n.625G>C
ENST00000640681.1:n.1247G>C
ENST00000652046.1:c.*118G>C MANE Select	ENSP00000498466.1:n.*118G>C
ENST00000352159.8:c.*443G>C	ENSP00000345601.4:n.*443G>C
ENST00000355740.6:c.*118G>C	ENSP00000347979.2:n.*118G>C
ENST00000479522.5:c.*555G>C	ENSP00000424113.1:n.*555G>C
ENST00000484444.5:c.*567G>C	ENSP00000420975.1:n.*567G>C
ENST00000494410.5:c.*484G>C	ENSP00000423755.1:n.*484G>C
NM_000043.4:c.*118G>C , LRG_134t1:c.*118G>C	NP_000034.1:n.*118G>C
NM_152871.2:c.*118G>C	NP_690610.1:n.*118G>C
NM_152872.2:c.*438G>C	NP_690611.1:n.*438G>C
NR_028033.2:n.1300G>C
NR_028034.2:n.1162G>C
NR_028035.2:n.1225G>C
NR_028036.2:n.1363G>C
XM_006717819.2:c.*118G>C	XP_006717882.1:n.*118G>C
XM_011539764.1:c.*118G>C	XP_011538066.1:n.*118G>C
XM_011539765.1:c.*118G>C	XP_011538067.1:n.*118G>C
XM_011539766.1:c.*118G>C	XP_011538068.1:n.*118G>C
XM_011539767.1:c.*118G>C	XP_011538069.1:n.*118G>C
NM_000043.5:c.*118G>C	NP_000034.1:n.*118G>C
NM_001320619.1:c.*449G>C	NP_001307548.1:n.*449G>C
NM_152871.3:c.*118G>C	NP_690610.1:n.*118G>C
NM_152872.3:c.*438G>C	NP_690611.1:n.*438G>C
NR_028033.3:n.1272G>C
NR_028034.3:n.1134G>C
NR_028035.3:n.1197G>C
NR_028036.3:n.1335G>C
NR_135313.1:n.1252G>C
NR_135314.1:n.1435G>C
NR_135315.1:n.1188G>C
XM_006717819.3:c.*118G>C	XP_006717882.1:n.*118G>C
XM_011539764.2:c.*118G>C	XP_011538066.1:n.*118G>C
XM_011539765.2:c.*118G>C	XP_011538067.1:n.*118G>C
XM_011539766.2:c.*118G>C	XP_011538068.1:n.*118G>C
XM_011539767.3:c.*118G>C	XP_011538069.1:n.*118G>C
XR_945732.3:n.1194G>C
XR_945733.2:n.1131G>C
NM_000043.6:c.*118G>C MANE Select	NP_000034.1:n.*118G>C
NM_001320619.2:c.*449G>C	NP_001307548.1:n.*449G>C
NM_152871.4:c.*118G>C	NP_690610.1:n.*118G>C
NM_152872.4:c.*438G>C	NP_690611.1:n.*438G>C
NR_028033.4:n.1033G>C
NR_028034.4:n.895G>C
NR_028035.4:n.958G>C
NR_028036.4:n.1096G>C
NR_135313.2:n.1013G>C
NR_135314.2:n.1292G>C
NR_135315.2:n.1045G>C