Canonical Allele Identifier: CA377510008

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774072T>G (hg19) ; chr10:g.89014315T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014315T>G , CM000672.2:g.89014315T>G	GRCh38
NC_000010.10:g.90774072T>G , CM000672.1:g.90774072T>G	GRCh37
NC_000010.9:g.90764052T>G	NCBI36
NG_009089.2:g.28785T>G , LRG_134:g.28785T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1182T>G
ENST00000355740.8:c.*196T>G	ENSP00000347979.3:n.*196T>G
ENST00000357339.7:c.810T>G	ENSP00000349896.2:p.Tyr270Ter
ENST00000371857.8:n.2418T>G
ENST00000460510.6:c.156T>G	ENSP00000512812.1:p.Tyr52Ter
ENST00000466081.6:n.2522T>G
ENST00000477270.6:c.918T>G	ENSP00000512813.1:p.Tyr306Ter
ENST00000479522.6:c.*302T>G	ENSP00000424113.1:n.*302T>G
ENST00000484444.6:c.*314T>G	ENSP00000420975.1:n.*314T>G
ENST00000488877.6:c.764T>G	ENSP00000425159.1:n.764T>G
ENST00000492756.7:c.*302T>G	ENSP00000422453.1:n.*302T>G
ENST00000494799.6:c.156T>G	ENSP00000512834.1:p.Tyr52Ter
ENST00000562983.3:c.156T>G	ENSP00000512845.1:p.Tyr52Ter
ENST00000612663.6:c.*275T>G	ENSP00000477997.3:n.*275T>G
ENST00000640140.2:n.1018T>G
ENST00000640250.2:n.372T>G
ENST00000640681.2:n.977T>G
ENST00000696723.1:n.4506T>G
ENST00000696741.1:n.2511T>G
ENST00000696742.1:n.2238T>G
ENST00000696743.1:n.3641T>G
ENST00000696744.1:n.912T>G
ENST00000696767.1:n.1207T>G
ENST00000696768.1:c.*196T>G	ENSP00000512859.1:n.*196T>G
ENST00000696769.1:n.2562T>G
ENST00000696771.1:c.156T>G	ENSP00000512860.1:p.Tyr52Ter
ENST00000696772.1:n.2476T>G
ENST00000696773.1:n.2215T>G
ENST00000696774.1:n.5983T>G
ENST00000696776.1:c.966T>G	ENSP00000512861.1:p.Tyr322Ter
ENST00000696777.1:n.2281T>G
ENST00000696778.1:n.1309T>G
ENST00000696779.1:c.480T>G	ENSP00000512862.1:p.Tyr160Ter
ENST00000696780.1:c.903T>G	ENSP00000512863.1:p.Tyr301Ter
ENST00000696781.1:c.618T>G	ENSP00000512864.1:p.Tyr206Ter
ENST00000696782.1:c.*275T>G	ENSP00000512865.1:n.*275T>G
ENST00000696783.1:n.2741T>G
ENST00000696992.1:n.1990T>G
ENST00000696995.1:n.4402T>G
ENST00000696996.1:n.2315T>G
ENST00000696997.1:c.*503T>G	ENSP00000513028.1:n.*503T>G
ENST00000696998.1:n.2127T>G
ENST00000696999.1:c.156T>G	ENSP00000513029.1:p.Tyr52Ter
ENST00000697036.1:c.*289T>G	ENSP00000513060.1:n.*289T>G
ENST00000697037.1:n.908T>G
ENST00000697093.1:n.3109T>G
ENST00000697094.1:n.3456T>G
ENST00000697095.1:c.*2074T>G	ENSP00000513104.1:n.*2074T>G
ENST00000697096.1:n.2006T>G
ENST00000697097.1:c.156T>G	ENSP00000513105.1:p.Tyr52Ter
ENST00000562983.2:n.1059T>G
ENST00000690268.1:c.954T>G	ENSP00000509810.1:p.Tyr318Ter
ENST00000355740.7:c.*199T>G	ENSP00000347979.3:n.*199T>G
ENST00000612663.5:c.*275T>G	ENSP00000477997.3:n.*275T>G
ENST00000640140.1:n.1045T>G
ENST00000640250.1:n.372T>G
ENST00000640681.1:n.994T>G
ENST00000652046.1:c.873T>G MANE Select	ENSP00000498466.1:p.Tyr291Ter
ENST00000352159.8:c.*190T>G	ENSP00000345601.4:n.*190T>G
ENST00000355279.2:c.848T>G	ENSP00000347426.2:n.848T>G
ENST00000355740.6:c.873T>G	ENSP00000347979.2:p.Tyr291Ter
ENST00000357339.6:c.810T>G	ENSP00000349896.2:p.Tyr270Ter
ENST00000479522.5:c.*302T>G	ENSP00000424113.1:n.*302T>G
ENST00000484444.5:c.*314T>G	ENSP00000420975.1:n.*314T>G
ENST00000488877.5:c.*314T>G	ENSP00000425159.1:n.*314T>G
ENST00000492756.5:c.701T>G	ENSP00000422453.1:n.701T>G
ENST00000494410.5:c.*231T>G	ENSP00000423755.1:n.*231T>G
ENST00000612663.4:c.*220T>G	ENSP00000477997.2:n.*220T>G
NM_000043.4:c.873T>G , LRG_134t1:c.873T>G	NP_000034.1:p.Tyr291Ter
NM_152871.2:c.810T>G	NP_690610.1:p.Tyr270Ter
NM_152872.2:c.*185T>G	NP_690611.1:n.*185T>G
NR_028033.2:n.1047T>G
NR_028034.2:n.909T>G
NR_028035.2:n.972T>G
NR_028036.2:n.1110T>G
XM_006717819.2:c.954T>G	XP_006717882.1:p.Tyr318Ter
XM_011539764.1:c.1035T>G	XP_011538066.1:p.Tyr345Ter
XM_011539765.1:c.972T>G	XP_011538067.1:p.Tyr324Ter
XM_011539766.1:c.954T>G	XP_011538068.1:p.Tyr318Ter
XM_011539767.1:c.918T>G	XP_011538069.1:p.Tyr306Ter
XR_945732.1:n.941T>G
XR_945733.1:n.878T>G
NM_000043.5:c.873T>G	NP_000034.1:p.Tyr291Ter
NM_001320619.1:c.*196T>G	NP_001307548.1:n.*196T>G
NM_152871.3:c.810T>G	NP_690610.1:p.Tyr270Ter
NM_152872.3:c.*185T>G	NP_690611.1:n.*185T>G
NR_028033.3:n.1019T>G
NR_028034.3:n.881T>G
NR_028035.3:n.944T>G
NR_028036.3:n.1082T>G
NR_135313.1:n.999T>G
NR_135314.1:n.1182T>G
NR_135315.1:n.935T>G
XM_006717819.3:c.954T>G	XP_006717882.1:p.Tyr318Ter
XM_011539764.2:c.1035T>G	XP_011538066.1:p.Tyr345Ter
XM_011539765.2:c.972T>G	XP_011538067.1:p.Tyr324Ter
XM_011539766.2:c.954T>G	XP_011538068.1:p.Tyr318Ter
XM_011539767.3:c.918T>G	XP_011538069.1:p.Tyr306Ter
XR_945732.3:n.941T>G
XR_945733.2:n.878T>G
NM_000043.6:c.873T>G MANE Select	NP_000034.1:p.Tyr291Ter
NM_001320619.2:c.*196T>G	NP_001307548.1:n.*196T>G
NM_152871.4:c.810T>G	NP_690610.1:p.Tyr270Ter
NM_152872.4:c.*185T>G	NP_690611.1:n.*185T>G
NR_028033.4:n.780T>G
NR_028034.4:n.642T>G
NR_028035.4:n.705T>G
NR_028036.4:n.843T>G
NR_135313.2:n.760T>G
NR_135314.2:n.1039T>G
NR_135315.2:n.792T>G