Canonical Allele Identifier: CA377510313

Gene: FAS

Linked Data

• gnomAD v4: 10-89014450-G-T
• MyVariant Identifiers: chr10:g.90774207G>T (hg19) ; chr10:g.89014450G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014450G>T , CM000672.2:g.89014450G>T	GRCh38
NC_000010.10:g.90774207G>T , CM000672.1:g.90774207G>T	GRCh37
NC_000010.9:g.90764187G>T	NCBI36
NG_009089.2:g.28920G>T , LRG_134:g.28920G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1317G>T
ENST00000355740.8:c.*331G>T	ENSP00000347979.3:n.*331G>T
ENST00000357339.7:c.945G>T	ENSP00000349896.2:p.Ter315Tyr
ENST00000371857.8:n.2553G>T
ENST00000460510.6:c.291G>T	ENSP00000512812.1:p.Ter97Tyr
ENST00000466081.6:n.2657G>T
ENST00000477270.6:c.1053G>T	ENSP00000512813.1:p.Ter351Tyr
ENST00000479522.6:c.*437G>T	ENSP00000424113.1:n.*437G>T
ENST00000484444.6:c.*449G>T	ENSP00000420975.1:n.*449G>T
ENST00000488877.6:c.899G>T	ENSP00000425159.1:n.899G>T
ENST00000492756.7:c.*437G>T	ENSP00000422453.1:n.*437G>T
ENST00000494799.6:c.291G>T	ENSP00000512834.1:p.Ter97Tyr
ENST00000562983.3:c.291G>T	ENSP00000512845.1:p.Ter97Tyr
ENST00000612663.6:c.*410G>T	ENSP00000477997.3:n.*410G>T
ENST00000640140.2:n.1153G>T
ENST00000640250.2:n.507G>T
ENST00000640681.2:n.1112G>T
ENST00000696723.1:n.4641G>T
ENST00000696741.1:n.2646G>T
ENST00000696742.1:n.2373G>T
ENST00000696743.1:n.3776G>T
ENST00000696744.1:n.1047G>T
ENST00000696767.1:n.1342G>T
ENST00000696768.1:c.*331G>T	ENSP00000512859.1:n.*331G>T
ENST00000696769.1:n.2697G>T
ENST00000696771.1:c.291G>T	ENSP00000512860.1:p.Ter97Tyr
ENST00000696772.1:n.2611G>T
ENST00000696773.1:n.2350G>T
ENST00000696774.1:n.6118G>T
ENST00000696776.1:c.1101G>T	ENSP00000512861.1:p.Ter367Tyr
ENST00000696777.1:n.2416G>T
ENST00000696778.1:n.1444G>T
ENST00000696779.1:c.615G>T	ENSP00000512862.1:p.Ter205Tyr
ENST00000696780.1:c.1038G>T	ENSP00000512863.1:p.Ter346Tyr
ENST00000696781.1:c.753G>T	ENSP00000512864.1:p.Ter251Tyr
ENST00000696782.1:c.*410G>T	ENSP00000512865.1:n.*410G>T
ENST00000696783.1:n.2876G>T
ENST00000696992.1:n.2125G>T
ENST00000696995.1:n.4537G>T
ENST00000696996.1:n.2450G>T
ENST00000696997.1:c.*638G>T	ENSP00000513028.1:n.*638G>T
ENST00000696998.1:n.2262G>T
ENST00000696999.1:c.291G>T	ENSP00000513029.1:p.Ter97Tyr
ENST00000697036.1:c.*424G>T	ENSP00000513060.1:n.*424G>T
ENST00000697037.1:n.1043G>T
ENST00000697093.1:n.3244G>T
ENST00000697094.1:n.3591G>T
ENST00000697095.1:c.*2209G>T	ENSP00000513104.1:n.*2209G>T
ENST00000697096.1:n.2141G>T
ENST00000697097.1:c.291G>T	ENSP00000513105.1:p.Ter97Tyr
ENST00000562983.2:n.1194G>T
ENST00000690268.1:c.1089G>T	ENSP00000509810.1:p.Ter363Tyr
ENST00000355740.7:c.*334G>T	ENSP00000347979.3:n.*334G>T
ENST00000612663.5:c.*410G>T	ENSP00000477997.3:n.*410G>T
ENST00000640140.1:n.1180G>T
ENST00000640250.1:n.507G>T
ENST00000640681.1:n.1129G>T
ENST00000652046.1:c.1008G>T MANE Select	ENSP00000498466.1:p.Ter336Tyr
ENST00000352159.8:c.*325G>T	ENSP00000345601.4:n.*325G>T
ENST00000355279.2:c.983G>T	ENSP00000347426.2:n.983G>T
ENST00000355740.6:c.1008G>T	ENSP00000347979.2:p.Ter336Tyr
ENST00000357339.6:c.945G>T	ENSP00000349896.2:p.Ter315Tyr
ENST00000479522.5:c.*437G>T	ENSP00000424113.1:n.*437G>T
ENST00000484444.5:c.*449G>T	ENSP00000420975.1:n.*449G>T
ENST00000488877.5:c.*449G>T	ENSP00000425159.1:n.*449G>T
ENST00000492756.5:c.836G>T	ENSP00000422453.1:n.836G>T
ENST00000494410.5:c.*366G>T	ENSP00000423755.1:n.*366G>T
ENST00000612663.4:c.*355G>T	ENSP00000477997.2:n.*355G>T
NM_000043.4:c.1008G>T , LRG_134t1:c.1008G>T	NP_000034.1:p.Ter336Tyr
NM_152871.2:c.945G>T	NP_690610.1:p.Ter315Tyr
NM_152872.2:c.*320G>T	NP_690611.1:n.*320G>T
NR_028033.2:n.1182G>T
NR_028034.2:n.1044G>T
NR_028035.2:n.1107G>T
NR_028036.2:n.1245G>T
XM_006717819.2:c.1089G>T	XP_006717882.1:p.Ter363Tyr
XM_011539764.1:c.1170G>T	XP_011538066.1:p.Ter390Tyr
XM_011539765.1:c.1107G>T	XP_011538067.1:p.Ter369Tyr
XM_011539766.1:c.1089G>T	XP_011538068.1:p.Ter363Tyr
XM_011539767.1:c.1053G>T	XP_011538069.1:p.Ter351Tyr
XR_945733.1:n.1013G>T
NM_000043.5:c.1008G>T	NP_000034.1:p.Ter336Tyr
NM_001320619.1:c.*331G>T	NP_001307548.1:n.*331G>T
NM_152871.3:c.945G>T	NP_690610.1:p.Ter315Tyr
NM_152872.3:c.*320G>T	NP_690611.1:n.*320G>T
NR_028033.3:n.1154G>T
NR_028034.3:n.1016G>T
NR_028035.3:n.1079G>T
NR_028036.3:n.1217G>T
NR_135313.1:n.1134G>T
NR_135314.1:n.1317G>T
NR_135315.1:n.1070G>T
XM_006717819.3:c.1089G>T	XP_006717882.1:p.Ter363Tyr
XM_011539764.2:c.1170G>T	XP_011538066.1:p.Ter390Tyr
XM_011539765.2:c.1107G>T	XP_011538067.1:p.Ter369Tyr
XM_011539766.2:c.1089G>T	XP_011538068.1:p.Ter363Tyr
XM_011539767.3:c.1053G>T	XP_011538069.1:p.Ter351Tyr
XR_945732.3:n.1076G>T
XR_945733.2:n.1013G>T
NM_000043.6:c.1008G>T MANE Select	NP_000034.1:p.Ter336Tyr
NM_001320619.2:c.*331G>T	NP_001307548.1:n.*331G>T
NM_152871.4:c.945G>T	NP_690610.1:p.Ter315Tyr
NM_152872.4:c.*320G>T	NP_690611.1:n.*320G>T
NR_028033.4:n.915G>T
NR_028034.4:n.777G>T
NR_028035.4:n.840G>T
NR_028036.4:n.978G>T
NR_135313.2:n.895G>T
NR_135314.2:n.1174G>T
NR_135315.2:n.927G>T