Canonical Allele Identifier: CA2610079810

Gene: FAS

Linked Data

• gnomAD v4: 10-89014672-GTGGCATGCTAAGTACCCAAATAGGAGTGTATGCAGAGGATGAAAGATTAAGATTATGCTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014679_89014738del , CM000672.2:g.89014679_89014738del	GRCh38
NC_000010.10:g.90774436_90774495del , CM000672.1:g.90774436_90774495del	GRCh37
NC_000010.9:g.90764416_90764475del	NCBI36
NG_009089.2:g.29149_29208del , LRG_134:g.29149_29208del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1546_1605del
ENST00000355740.8:c.*560_*619del	ENSP00000347979.3:n.*560_*619del
ENST00000357339.7:c.*229_*288del	ENSP00000349896.2:n.*229_*288del
ENST00000371857.8:n.2782_2841del
ENST00000460510.6:c.*229_*288del	ENSP00000512812.1:n.*229_*288del
ENST00000466081.6:n.2886_2945del
ENST00000477270.6:c.*229_*288del	ENSP00000512813.1:n.*229_*288del
ENST00000492756.7:c.*666_*725del	ENSP00000422453.1:n.*666_*725del
ENST00000494799.6:c.*229_*288del	ENSP00000512834.1:n.*229_*288del
ENST00000562983.3:c.*229_*288del	ENSP00000512845.1:n.*229_*288del
ENST00000612663.6:c.*639_*698del	ENSP00000477997.3:n.*639_*698del
ENST00000640140.2:n.1382_1441del
ENST00000640250.2:n.736_795del
ENST00000640681.2:n.1341_1400del
ENST00000696723.1:n.4870_4929del
ENST00000696741.1:n.2875_2934del
ENST00000696742.1:n.2602_2661del
ENST00000696743.1:n.4005_4064del
ENST00000696744.1:n.1276_1335del
ENST00000696767.1:n.1571_1630del
ENST00000696768.1:c.*560_*619del	ENSP00000512859.1:n.*560_*619del
ENST00000696771.1:c.*229_*288del	ENSP00000512860.1:n.*229_*288del
ENST00000696772.1:n.2840_2899del
ENST00000696773.1:n.2579_2638del
ENST00000696774.1:n.6347_6406del
ENST00000696776.1:c.*229_*288del	ENSP00000512861.1:n.*229_*288del
ENST00000696777.1:n.2645_2704del
ENST00000696778.1:n.1673_1732del
ENST00000696779.1:c.*229_*288del	ENSP00000512862.1:n.*229_*288del
ENST00000696780.1:c.*229_*288del	ENSP00000512863.1:n.*229_*288del
ENST00000696781.1:c.*229_*288del	ENSP00000512864.1:n.*229_*288del
ENST00000696782.1:c.*639_*698del	ENSP00000512865.1:n.*639_*698del
ENST00000696783.1:n.3105_3164del
ENST00000696992.1:n.2354_2413del
ENST00000696995.1:n.4766_4825del
ENST00000696996.1:n.2679_2738del
ENST00000696997.1:c.*867_*926del	ENSP00000513028.1:n.*867_*926del
ENST00000696998.1:n.2491_2550del
ENST00000696999.1:c.*229_*288del	ENSP00000513029.1:n.*229_*288del
ENST00000697036.1:c.*653_*712del	ENSP00000513060.1:n.*653_*712del
ENST00000697037.1:n.1272_1331del
ENST00000697093.1:n.3473_3532del
ENST00000697094.1:n.3820_3879del
ENST00000697095.1:c.*2438_*2497del	ENSP00000513104.1:n.*2438_*2497del
ENST00000697096.1:n.2370_2429del
ENST00000697097.1:c.*229_*288del	ENSP00000513105.1:n.*229_*288del
ENST00000562983.2:n.1423_1482del
ENST00000690268.1:c.*229_*288del	ENSP00000509810.1:n.*229_*288del
ENST00000355740.7:c.*563_*622del	ENSP00000347979.3:n.*563_*622del
ENST00000640140.1:n.1409_1468del
ENST00000640250.1:n.736_795del
ENST00000640681.1:n.1358_1417del
ENST00000652046.1:c.*229_*288del MANE Select	ENSP00000498466.1:n.*229_*288del
ENST00000352159.8:c.*554_*613del	ENSP00000345601.4:n.*554_*613del
ENST00000355740.6:c.*229_*288del	ENSP00000347979.2:n.*229_*288del
NM_000043.4:c.*229_*288del , LRG_134t1:c.*229_*288del	NP_000034.1:n.*229_*288del
NM_152871.2:c.*229_*288del	NP_690610.1:n.*229_*288del
NM_152872.2:c.*549_*608del	NP_690611.1:n.*549_*608del
NR_028033.2:n.1411_1470del
NR_028034.2:n.1273_1332del
NR_028035.2:n.1336_1395del
NR_028036.2:n.1474_1533del
XM_006717819.2:c.*229_*288del	XP_006717882.1:n.*229_*288del
XM_011539764.1:c.*229_*288del	XP_011538066.1:n.*229_*288del
XM_011539765.1:c.*229_*288del	XP_011538067.1:n.*229_*288del
XM_011539766.1:c.*229_*288del	XP_011538068.1:n.*229_*288del
XM_011539767.1:c.*229_*288del	XP_011538069.1:n.*229_*288del
NM_000043.5:c.*229_*288del	NP_000034.1:n.*229_*288del
NM_001320619.1:c.*560_*619del	NP_001307548.1:n.*560_*619del
NM_152871.3:c.*229_*288del	NP_690610.1:n.*229_*288del
NM_152872.3:c.*549_*608del	NP_690611.1:n.*549_*608del
NR_028033.3:n.1383_1442del
NR_028034.3:n.1245_1304del
NR_028035.3:n.1308_1367del
NR_028036.3:n.1446_1505del
NR_135313.1:n.1363_1422del
NR_135314.1:n.1546_1605del
NR_135315.1:n.1299_1358del
XM_006717819.3:c.*229_*288del	XP_006717882.1:n.*229_*288del
XM_011539764.2:c.*229_*288del	XP_011538066.1:n.*229_*288del
XM_011539765.2:c.*229_*288del	XP_011538067.1:n.*229_*288del
XM_011539766.2:c.*229_*288del	XP_011538068.1:n.*229_*288del
XM_011539767.3:c.*229_*288del	XP_011538069.1:n.*229_*288del
XR_945732.3:n.1305_1364del
XR_945733.2:n.1242_1301del
NM_000043.6:c.*229_*288del MANE Select	NP_000034.1:n.*229_*288del
NM_001320619.2:c.*560_*619del	NP_001307548.1:n.*560_*619del
NM_152871.4:c.*229_*288del	NP_690610.1:n.*229_*288del
NM_152872.4:c.*549_*608del	NP_690611.1:n.*549_*608del
NR_028033.4:n.1144_1203del
NR_028034.4:n.1006_1065del
NR_028035.4:n.1069_1128del
NR_028036.4:n.1207_1266del
NR_135313.2:n.1124_1183del
NR_135314.2:n.1403_1462del
NR_135315.2:n.1156_1215del