Canonical Allele Identifier: CA377510001

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774070T>C (hg19) ; chr10:g.89014313T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014313T>C , CM000672.2:g.89014313T>C	GRCh38
NC_000010.10:g.90774070T>C , CM000672.1:g.90774070T>C	GRCh37
NC_000010.9:g.90764050T>C	NCBI36
NG_009089.2:g.28783T>C , LRG_134:g.28783T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1180T>C
ENST00000355740.8:c.*194T>C	ENSP00000347979.3:n.*194T>C
ENST00000357339.7:c.808T>C	ENSP00000349896.2:p.Tyr270His
ENST00000371857.8:n.2416T>C
ENST00000460510.6:c.154T>C	ENSP00000512812.1:p.Tyr52His
ENST00000466081.6:n.2520T>C
ENST00000477270.6:c.916T>C	ENSP00000512813.1:p.Tyr306His
ENST00000479522.6:c.*300T>C	ENSP00000424113.1:n.*300T>C
ENST00000484444.6:c.*312T>C	ENSP00000420975.1:n.*312T>C
ENST00000488877.6:c.762T>C	ENSP00000425159.1:n.762T>C
ENST00000492756.7:c.*300T>C	ENSP00000422453.1:n.*300T>C
ENST00000494799.6:c.154T>C	ENSP00000512834.1:p.Tyr52His
ENST00000562983.3:c.154T>C	ENSP00000512845.1:p.Tyr52His
ENST00000612663.6:c.*273T>C	ENSP00000477997.3:n.*273T>C
ENST00000640140.2:n.1016T>C
ENST00000640250.2:n.370T>C
ENST00000640681.2:n.975T>C
ENST00000696723.1:n.4504T>C
ENST00000696741.1:n.2509T>C
ENST00000696742.1:n.2236T>C
ENST00000696743.1:n.3639T>C
ENST00000696744.1:n.910T>C
ENST00000696767.1:n.1205T>C
ENST00000696768.1:c.*194T>C	ENSP00000512859.1:n.*194T>C
ENST00000696769.1:n.2560T>C
ENST00000696771.1:c.154T>C	ENSP00000512860.1:p.Tyr52His
ENST00000696772.1:n.2474T>C
ENST00000696773.1:n.2213T>C
ENST00000696774.1:n.5981T>C
ENST00000696776.1:c.964T>C	ENSP00000512861.1:p.Tyr322His
ENST00000696777.1:n.2279T>C
ENST00000696778.1:n.1307T>C
ENST00000696779.1:c.478T>C	ENSP00000512862.1:p.Tyr160His
ENST00000696780.1:c.901T>C	ENSP00000512863.1:p.Tyr301His
ENST00000696781.1:c.616T>C	ENSP00000512864.1:p.Tyr206His
ENST00000696782.1:c.*273T>C	ENSP00000512865.1:n.*273T>C
ENST00000696783.1:n.2739T>C
ENST00000696992.1:n.1988T>C
ENST00000696995.1:n.4400T>C
ENST00000696996.1:n.2313T>C
ENST00000696997.1:c.*501T>C	ENSP00000513028.1:n.*501T>C
ENST00000696998.1:n.2125T>C
ENST00000696999.1:c.154T>C	ENSP00000513029.1:p.Tyr52His
ENST00000697036.1:c.*287T>C	ENSP00000513060.1:n.*287T>C
ENST00000697037.1:n.906T>C
ENST00000697093.1:n.3107T>C
ENST00000697094.1:n.3454T>C
ENST00000697095.1:c.*2072T>C	ENSP00000513104.1:n.*2072T>C
ENST00000697096.1:n.2004T>C
ENST00000697097.1:c.154T>C	ENSP00000513105.1:p.Tyr52His
ENST00000562983.2:n.1057T>C
ENST00000690268.1:c.952T>C	ENSP00000509810.1:p.Tyr318His
ENST00000355740.7:c.*197T>C	ENSP00000347979.3:n.*197T>C
ENST00000612663.5:c.*273T>C	ENSP00000477997.3:n.*273T>C
ENST00000640140.1:n.1043T>C
ENST00000640250.1:n.370T>C
ENST00000640681.1:n.992T>C
ENST00000652046.1:c.871T>C MANE Select	ENSP00000498466.1:p.Tyr291His
ENST00000352159.8:c.*188T>C	ENSP00000345601.4:n.*188T>C
ENST00000355279.2:c.846T>C	ENSP00000347426.2:n.846T>C
ENST00000355740.6:c.871T>C	ENSP00000347979.2:p.Tyr291His
ENST00000357339.6:c.808T>C	ENSP00000349896.2:p.Tyr270His
ENST00000479522.5:c.*300T>C	ENSP00000424113.1:n.*300T>C
ENST00000484444.5:c.*312T>C	ENSP00000420975.1:n.*312T>C
ENST00000488877.5:c.*312T>C	ENSP00000425159.1:n.*312T>C
ENST00000492756.5:c.699T>C	ENSP00000422453.1:n.699T>C
ENST00000494410.5:c.*229T>C	ENSP00000423755.1:n.*229T>C
ENST00000612663.4:c.*218T>C	ENSP00000477997.2:n.*218T>C
NM_000043.4:c.871T>C , LRG_134t1:c.871T>C	NP_000034.1:p.Tyr291His
NM_152871.2:c.808T>C	NP_690610.1:p.Tyr270His
NM_152872.2:c.*183T>C	NP_690611.1:n.*183T>C
NR_028033.2:n.1045T>C
NR_028034.2:n.907T>C
NR_028035.2:n.970T>C
NR_028036.2:n.1108T>C
XM_006717819.2:c.952T>C	XP_006717882.1:p.Tyr318His
XM_011539764.1:c.1033T>C	XP_011538066.1:p.Tyr345His
XM_011539765.1:c.970T>C	XP_011538067.1:p.Tyr324His
XM_011539766.1:c.952T>C	XP_011538068.1:p.Tyr318His
XM_011539767.1:c.916T>C	XP_011538069.1:p.Tyr306His
XR_945732.1:n.939T>C
XR_945733.1:n.876T>C
NM_000043.5:c.871T>C	NP_000034.1:p.Tyr291His
NM_001320619.1:c.*194T>C	NP_001307548.1:n.*194T>C
NM_152871.3:c.808T>C	NP_690610.1:p.Tyr270His
NM_152872.3:c.*183T>C	NP_690611.1:n.*183T>C
NR_028033.3:n.1017T>C
NR_028034.3:n.879T>C
NR_028035.3:n.942T>C
NR_028036.3:n.1080T>C
NR_135313.1:n.997T>C
NR_135314.1:n.1180T>C
NR_135315.1:n.933T>C
XM_006717819.3:c.952T>C	XP_006717882.1:p.Tyr318His
XM_011539764.2:c.1033T>C	XP_011538066.1:p.Tyr345His
XM_011539765.2:c.970T>C	XP_011538067.1:p.Tyr324His
XM_011539766.2:c.952T>C	XP_011538068.1:p.Tyr318His
XM_011539767.3:c.916T>C	XP_011538069.1:p.Tyr306His
XR_945732.3:n.939T>C
XR_945733.2:n.876T>C
NM_000043.6:c.871T>C MANE Select	NP_000034.1:p.Tyr291His
NM_001320619.2:c.*194T>C	NP_001307548.1:n.*194T>C
NM_152871.4:c.808T>C	NP_690610.1:p.Tyr270His
NM_152872.4:c.*183T>C	NP_690611.1:n.*183T>C
NR_028033.4:n.778T>C
NR_028034.4:n.640T>C
NR_028035.4:n.703T>C
NR_028036.4:n.841T>C
NR_135313.2:n.758T>C
NR_135314.2:n.1037T>C
NR_135315.2:n.790T>C