Canonical Allele Identifier: CA594943249

Gene: FAS

Linked Data

• dbSNP Id: rs1223310407
• gnomAD v2: 10-90774314-CATTT-C
• gnomAD v4: 10-89014557-CATTT-C
• MyVariant Identifiers: chr10:g.90774315_90774318del (hg19) ; chr10:g.89014558_89014561del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014561_89014564del , CM000672.2:g.89014561_89014564del	GRCh38
NC_000010.10:g.90774318_90774321del , CM000672.1:g.90774318_90774321del	GRCh37
NC_000010.9:g.90764298_90764301del	NCBI36
NG_009089.2:g.29031_29034del , LRG_134:g.29031_29034del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1428_1431del
ENST00000355740.8:c.*442_*445del	ENSP00000347979.3:n.*442_*445del
ENST00000357339.7:c.*111_*114del	ENSP00000349896.2:n.*111_*114del
ENST00000371857.8:n.2664_2667del
ENST00000460510.6:c.*111_*114del	ENSP00000512812.1:n.*111_*114del
ENST00000466081.6:n.2768_2771del
ENST00000477270.6:c.*111_*114del	ENSP00000512813.1:n.*111_*114del
ENST00000479522.6:c.*548_*551del	ENSP00000424113.1:n.*548_*551del
ENST00000484444.6:c.*560_*563del	ENSP00000420975.1:n.*560_*563del
ENST00000488877.6:c.1010_1013del	ENSP00000425159.1:n.1010_1013del
ENST00000492756.7:c.*548_*551del	ENSP00000422453.1:n.*548_*551del
ENST00000494799.6:c.*111_*114del	ENSP00000512834.1:n.*111_*114del
ENST00000562983.3:c.*111_*114del	ENSP00000512845.1:n.*111_*114del
ENST00000612663.6:c.*521_*524del	ENSP00000477997.3:n.*521_*524del
ENST00000640140.2:n.1264_1267del
ENST00000640250.2:n.618_621del
ENST00000640681.2:n.1223_1226del
ENST00000696723.1:n.4752_4755del
ENST00000696741.1:n.2757_2760del
ENST00000696742.1:n.2484_2487del
ENST00000696743.1:n.3887_3890del
ENST00000696744.1:n.1158_1161del
ENST00000696767.1:n.1453_1456del
ENST00000696768.1:c.*442_*445del	ENSP00000512859.1:n.*442_*445del
ENST00000696769.1:n.2808_2811del
ENST00000696771.1:c.*111_*114del	ENSP00000512860.1:n.*111_*114del
ENST00000696772.1:n.2722_2725del
ENST00000696773.1:n.2461_2464del
ENST00000696774.1:n.6229_6232del
ENST00000696776.1:c.*111_*114del	ENSP00000512861.1:n.*111_*114del
ENST00000696777.1:n.2527_2530del
ENST00000696778.1:n.1555_1558del
ENST00000696779.1:c.*111_*114del	ENSP00000512862.1:n.*111_*114del
ENST00000696780.1:c.*111_*114del	ENSP00000512863.1:n.*111_*114del
ENST00000696781.1:c.*111_*114del	ENSP00000512864.1:n.*111_*114del
ENST00000696782.1:c.*521_*524del	ENSP00000512865.1:n.*521_*524del
ENST00000696783.1:n.2987_2990del
ENST00000696992.1:n.2236_2239del
ENST00000696995.1:n.4648_4651del
ENST00000696996.1:n.2561_2564del
ENST00000696997.1:c.*749_*752del	ENSP00000513028.1:n.*749_*752del
ENST00000696998.1:n.2373_2376del
ENST00000696999.1:c.*111_*114del	ENSP00000513029.1:n.*111_*114del
ENST00000697036.1:c.*535_*538del	ENSP00000513060.1:n.*535_*538del
ENST00000697037.1:n.1154_1157del
ENST00000697093.1:n.3355_3358del
ENST00000697094.1:n.3702_3705del
ENST00000697095.1:c.*2320_*2323del	ENSP00000513104.1:n.*2320_*2323del
ENST00000697096.1:n.2252_2255del
ENST00000697097.1:c.*111_*114del	ENSP00000513105.1:n.*111_*114del
ENST00000562983.2:n.1305_1308del
ENST00000690268.1:c.*111_*114del	ENSP00000509810.1:n.*111_*114del
ENST00000355740.7:c.*445_*448del	ENSP00000347979.3:n.*445_*448del
ENST00000640140.1:n.1291_1294del
ENST00000640250.1:n.618_621del
ENST00000640681.1:n.1240_1243del
ENST00000652046.1:c.*111_*114del MANE Select	ENSP00000498466.1:n.*111_*114del
ENST00000352159.8:c.*436_*439del	ENSP00000345601.4:n.*436_*439del
ENST00000355740.6:c.*111_*114del	ENSP00000347979.2:n.*111_*114del
ENST00000479522.5:c.*548_*551del	ENSP00000424113.1:n.*548_*551del
ENST00000484444.5:c.*560_*563del	ENSP00000420975.1:n.*560_*563del
ENST00000494410.5:c.*477_*480del	ENSP00000423755.1:n.*477_*480del
NM_000043.4:c.*111_*114del , LRG_134t1:c.*111_*114del	NP_000034.1:n.*111_*114del
NM_152871.2:c.*111_*114del	NP_690610.1:n.*111_*114del
NM_152872.2:c.*431_*434del	NP_690611.1:n.*431_*434del
NR_028033.2:n.1293_1296del
NR_028034.2:n.1155_1158del
NR_028035.2:n.1218_1221del
NR_028036.2:n.1356_1359del
XM_006717819.2:c.*111_*114del	XP_006717882.1:n.*111_*114del
XM_011539764.1:c.*111_*114del	XP_011538066.1:n.*111_*114del
XM_011539765.1:c.*111_*114del	XP_011538067.1:n.*111_*114del
XM_011539766.1:c.*111_*114del	XP_011538068.1:n.*111_*114del
XM_011539767.1:c.*111_*114del	XP_011538069.1:n.*111_*114del
NM_000043.5:c.*111_*114del	NP_000034.1:n.*111_*114del
NM_001320619.1:c.*442_*445del	NP_001307548.1:n.*442_*445del
NM_152871.3:c.*111_*114del	NP_690610.1:n.*111_*114del
NM_152872.3:c.*431_*434del	NP_690611.1:n.*431_*434del
NR_028033.3:n.1265_1268del
NR_028034.3:n.1127_1130del
NR_028035.3:n.1190_1193del
NR_028036.3:n.1328_1331del
NR_135313.1:n.1245_1248del
NR_135314.1:n.1428_1431del
NR_135315.1:n.1181_1184del
XM_006717819.3:c.*111_*114del	XP_006717882.1:n.*111_*114del
XM_011539764.2:c.*111_*114del	XP_011538066.1:n.*111_*114del
XM_011539765.2:c.*111_*114del	XP_011538067.1:n.*111_*114del
XM_011539766.2:c.*111_*114del	XP_011538068.1:n.*111_*114del
XM_011539767.3:c.*111_*114del	XP_011538069.1:n.*111_*114del
XR_945732.3:n.1187_1190del
XR_945733.2:n.1124_1127del
NM_000043.6:c.*111_*114del MANE Select	NP_000034.1:n.*111_*114del
NM_001320619.2:c.*442_*445del	NP_001307548.1:n.*442_*445del
NM_152871.4:c.*111_*114del	NP_690610.1:n.*111_*114del
NM_152872.4:c.*431_*434del	NP_690611.1:n.*431_*434del
NR_028033.4:n.1026_1029del
NR_028034.4:n.888_891del
NR_028035.4:n.951_954del
NR_028036.4:n.1089_1092del
NR_135313.2:n.1006_1009del
NR_135314.2:n.1285_1288del
NR_135315.2:n.1038_1041del