Canonical Allele Identifier: CA470974982

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773979T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014222T>C , CM000672.2:g.89014222T>C	GRCh38
NC_000010.10:g.90773979T>C , CM000672.1:g.90773979T>C	GRCh37
NC_000010.9:g.90763959T>C	NCBI36
NG_009089.2:g.28692T>C , LRG_134:g.28692T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1089T>C
ENST00000355740.8:c.*103T>C	ENSP00000347979.3:n.*103T>C
ENST00000357339.7:c.717T>C	ENSP00000349896.2:p.Asp239=
ENST00000371857.8:n.2325T>C
ENST00000460510.6:c.63T>C	ENSP00000512812.1:p.Asp21=
ENST00000466081.6:n.2429T>C
ENST00000477270.6:c.825T>C	ENSP00000512813.1:p.Asp275=
ENST00000479522.6:c.*209T>C	ENSP00000424113.1:n.*209T>C
ENST00000484444.6:c.*221T>C	ENSP00000420975.1:n.*221T>C
ENST00000488877.6:c.671T>C	ENSP00000425159.1:n.671T>C
ENST00000492756.7:c.*209T>C	ENSP00000422453.1:n.*209T>C
ENST00000494799.6:c.63T>C	ENSP00000512834.1:p.Asp21=
ENST00000562983.3:c.63T>C	ENSP00000512845.1:p.Asp21=
ENST00000612663.6:c.*182T>C	ENSP00000477997.3:n.*182T>C
ENST00000640140.2:n.925T>C
ENST00000640250.2:n.279T>C
ENST00000640681.2:n.884T>C
ENST00000696723.1:n.4413T>C
ENST00000696741.1:n.2418T>C
ENST00000696742.1:n.2145T>C
ENST00000696743.1:n.3548T>C
ENST00000696744.1:n.819T>C
ENST00000696767.1:n.1114T>C
ENST00000696768.1:c.*103T>C	ENSP00000512859.1:n.*103T>C
ENST00000696769.1:n.2469T>C
ENST00000696771.1:c.63T>C	ENSP00000512860.1:p.Asp21=
ENST00000696772.1:n.2383T>C
ENST00000696773.1:n.2122T>C
ENST00000696774.1:n.5890T>C
ENST00000696776.1:c.873T>C	ENSP00000512861.1:p.Asp291=
ENST00000696777.1:n.2188T>C
ENST00000696778.1:n.1216T>C
ENST00000696779.1:c.387T>C	ENSP00000512862.1:p.Asp129=
ENST00000696780.1:c.810T>C	ENSP00000512863.1:p.Asp270=
ENST00000696781.1:c.525T>C	ENSP00000512864.1:p.Asp175=
ENST00000696782.1:c.*182T>C	ENSP00000512865.1:n.*182T>C
ENST00000696783.1:n.2648T>C
ENST00000696992.1:n.1897T>C
ENST00000696995.1:n.4309T>C
ENST00000696996.1:n.2222T>C
ENST00000696997.1:c.*410T>C	ENSP00000513028.1:n.*410T>C
ENST00000696998.1:n.2034T>C
ENST00000696999.1:c.63T>C	ENSP00000513029.1:p.Asp21=
ENST00000697035.1:c.*113T>C	ENSP00000513059.1:n.*113T>C
ENST00000697036.1:c.*196T>C	ENSP00000513060.1:n.*196T>C
ENST00000697037.1:n.815T>C
ENST00000697093.1:n.3016T>C
ENST00000697094.1:n.3363T>C
ENST00000697095.1:c.*1981T>C	ENSP00000513104.1:n.*1981T>C
ENST00000697096.1:n.1913T>C
ENST00000697097.1:c.63T>C	ENSP00000513105.1:p.Asp21=
ENST00000562983.2:n.966T>C
ENST00000690268.1:c.861T>C	ENSP00000509810.1:p.Asp287=
ENST00000355740.7:c.*106T>C	ENSP00000347979.3:n.*106T>C
ENST00000612663.5:c.*182T>C	ENSP00000477997.3:n.*182T>C
ENST00000640140.1:n.952T>C
ENST00000640250.1:n.279T>C
ENST00000640681.1:n.901T>C
ENST00000652046.1:c.780T>C MANE Select	ENSP00000498466.1:p.Asp260=
ENST00000352159.8:c.*97T>C	ENSP00000345601.4:n.*97T>C
ENST00000355279.2:c.755T>C	ENSP00000347426.2:n.755T>C
ENST00000355740.6:c.780T>C	ENSP00000347979.2:p.Asp260=
ENST00000357339.6:c.717T>C	ENSP00000349896.2:p.Asp239=
ENST00000479522.5:c.*209T>C	ENSP00000424113.1:n.*209T>C
ENST00000484444.5:c.*221T>C	ENSP00000420975.1:n.*221T>C
ENST00000488877.5:c.*221T>C	ENSP00000425159.1:n.*221T>C
ENST00000492756.5:c.608T>C	ENSP00000422453.1:n.608T>C
ENST00000494410.5:c.*138T>C	ENSP00000423755.1:n.*138T>C
ENST00000612663.4:c.*127T>C	ENSP00000477997.2:n.*127T>C
NM_000043.4:c.780T>C , LRG_134t1:c.780T>C	NP_000034.1:p.Asp260=
NM_152871.2:c.717T>C	NP_690610.1:p.Asp239=
NM_152872.2:c.*92T>C	NP_690611.1:n.*92T>C
NR_028033.2:n.954T>C
NR_028034.2:n.816T>C
NR_028035.2:n.879T>C
NR_028036.2:n.1017T>C
XM_006717819.2:c.861T>C	XP_006717882.1:p.Asp287=
XM_011539764.1:c.942T>C	XP_011538066.1:p.Asp314=
XM_011539765.1:c.879T>C	XP_011538067.1:p.Asp293=
XM_011539766.1:c.861T>C	XP_011538068.1:p.Asp287=
XM_011539767.1:c.825T>C	XP_011538069.1:p.Asp275=
XR_945732.1:n.848T>C
XR_945733.1:n.785T>C
NM_000043.5:c.780T>C	NP_000034.1:p.Asp260=
NM_001320619.1:c.*103T>C	NP_001307548.1:n.*103T>C
NM_152871.3:c.717T>C	NP_690610.1:p.Asp239=
NM_152872.3:c.*92T>C	NP_690611.1:n.*92T>C
NR_028033.3:n.926T>C
NR_028034.3:n.788T>C
NR_028035.3:n.851T>C
NR_028036.3:n.989T>C
NR_135313.1:n.906T>C
NR_135314.1:n.1089T>C
NR_135315.1:n.842T>C
XM_006717819.3:c.861T>C	XP_006717882.1:p.Asp287=
XM_011539764.2:c.942T>C	XP_011538066.1:p.Asp314=
XM_011539765.2:c.879T>C	XP_011538067.1:p.Asp293=
XM_011539766.2:c.861T>C	XP_011538068.1:p.Asp287=
XM_011539767.3:c.825T>C	XP_011538069.1:p.Asp275=
XR_945732.3:n.848T>C
XR_945733.2:n.785T>C
NM_000043.6:c.780T>C MANE Select	NP_000034.1:p.Asp260=
NM_001320619.2:c.*103T>C	NP_001307548.1:n.*103T>C
NM_152871.4:c.717T>C	NP_690610.1:p.Asp239=
NM_152872.4:c.*92T>C	NP_690611.1:n.*92T>C
NR_028033.4:n.687T>C
NR_028034.4:n.549T>C
NR_028035.4:n.612T>C
NR_028036.4:n.750T>C
NR_135313.2:n.667T>C
NR_135314.2:n.946T>C
NR_135315.2:n.699T>C