Canonical Allele Identifier: CA470974937

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774114T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014357T>C , CM000672.2:g.89014357T>C	GRCh38
NC_000010.10:g.90774114T>C , CM000672.1:g.90774114T>C	GRCh37
NC_000010.9:g.90764094T>C	NCBI36
NG_009089.2:g.28827T>C , LRG_134:g.28827T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1224T>C
ENST00000355740.8:c.*238T>C	ENSP00000347979.3:n.*238T>C
ENST00000357339.7:c.852T>C	ENSP00000349896.2:p.Thr284=
ENST00000371857.8:n.2460T>C
ENST00000460510.6:c.198T>C	ENSP00000512812.1:p.Thr66=
ENST00000466081.6:n.2564T>C
ENST00000477270.6:c.960T>C	ENSP00000512813.1:p.Thr320=
ENST00000479522.6:c.*344T>C	ENSP00000424113.1:n.*344T>C
ENST00000484444.6:c.*356T>C	ENSP00000420975.1:n.*356T>C
ENST00000488877.6:c.806T>C	ENSP00000425159.1:n.806T>C
ENST00000492756.7:c.*344T>C	ENSP00000422453.1:n.*344T>C
ENST00000494799.6:c.198T>C	ENSP00000512834.1:p.Thr66=
ENST00000562983.3:c.198T>C	ENSP00000512845.1:p.Thr66=
ENST00000612663.6:c.*317T>C	ENSP00000477997.3:n.*317T>C
ENST00000640140.2:n.1060T>C
ENST00000640250.2:n.414T>C
ENST00000640681.2:n.1019T>C
ENST00000696723.1:n.4548T>C
ENST00000696741.1:n.2553T>C
ENST00000696742.1:n.2280T>C
ENST00000696743.1:n.3683T>C
ENST00000696744.1:n.954T>C
ENST00000696767.1:n.1249T>C
ENST00000696768.1:c.*238T>C	ENSP00000512859.1:n.*238T>C
ENST00000696769.1:n.2604T>C
ENST00000696771.1:c.198T>C	ENSP00000512860.1:p.Thr66=
ENST00000696772.1:n.2518T>C
ENST00000696773.1:n.2257T>C
ENST00000696774.1:n.6025T>C
ENST00000696776.1:c.1008T>C	ENSP00000512861.1:p.Thr336=
ENST00000696777.1:n.2323T>C
ENST00000696778.1:n.1351T>C
ENST00000696779.1:c.522T>C	ENSP00000512862.1:p.Thr174=
ENST00000696780.1:c.945T>C	ENSP00000512863.1:p.Thr315=
ENST00000696781.1:c.660T>C	ENSP00000512864.1:p.Thr220=
ENST00000696782.1:c.*317T>C	ENSP00000512865.1:n.*317T>C
ENST00000696783.1:n.2783T>C
ENST00000696992.1:n.2032T>C
ENST00000696995.1:n.4444T>C
ENST00000696996.1:n.2357T>C
ENST00000696997.1:c.*545T>C	ENSP00000513028.1:n.*545T>C
ENST00000696998.1:n.2169T>C
ENST00000696999.1:c.198T>C	ENSP00000513029.1:p.Thr66=
ENST00000697036.1:c.*331T>C	ENSP00000513060.1:n.*331T>C
ENST00000697037.1:n.950T>C
ENST00000697093.1:n.3151T>C
ENST00000697094.1:n.3498T>C
ENST00000697095.1:c.*2116T>C	ENSP00000513104.1:n.*2116T>C
ENST00000697096.1:n.2048T>C
ENST00000697097.1:c.198T>C	ENSP00000513105.1:p.Thr66=
ENST00000562983.2:n.1101T>C
ENST00000690268.1:c.996T>C	ENSP00000509810.1:p.Thr332=
ENST00000355740.7:c.*241T>C	ENSP00000347979.3:n.*241T>C
ENST00000612663.5:c.*317T>C	ENSP00000477997.3:n.*317T>C
ENST00000640140.1:n.1087T>C
ENST00000640250.1:n.414T>C
ENST00000640681.1:n.1036T>C
ENST00000652046.1:c.915T>C MANE Select	ENSP00000498466.1:p.Thr305=
ENST00000352159.8:c.*232T>C	ENSP00000345601.4:n.*232T>C
ENST00000355279.2:c.890T>C	ENSP00000347426.2:n.890T>C
ENST00000355740.6:c.915T>C	ENSP00000347979.2:p.Thr305=
ENST00000357339.6:c.852T>C	ENSP00000349896.2:p.Thr284=
ENST00000479522.5:c.*344T>C	ENSP00000424113.1:n.*344T>C
ENST00000484444.5:c.*356T>C	ENSP00000420975.1:n.*356T>C
ENST00000488877.5:c.*356T>C	ENSP00000425159.1:n.*356T>C
ENST00000492756.5:c.743T>C	ENSP00000422453.1:n.743T>C
ENST00000494410.5:c.*273T>C	ENSP00000423755.1:n.*273T>C
ENST00000612663.4:c.*262T>C	ENSP00000477997.2:n.*262T>C
NM_000043.4:c.915T>C , LRG_134t1:c.915T>C	NP_000034.1:p.Thr305=
NM_152871.2:c.852T>C	NP_690610.1:p.Thr284=
NM_152872.2:c.*227T>C	NP_690611.1:n.*227T>C
NR_028033.2:n.1089T>C
NR_028034.2:n.951T>C
NR_028035.2:n.1014T>C
NR_028036.2:n.1152T>C
XM_006717819.2:c.996T>C	XP_006717882.1:p.Thr332=
XM_011539764.1:c.1077T>C	XP_011538066.1:p.Thr359=
XM_011539765.1:c.1014T>C	XP_011538067.1:p.Thr338=
XM_011539766.1:c.996T>C	XP_011538068.1:p.Thr332=
XM_011539767.1:c.960T>C	XP_011538069.1:p.Thr320=
XR_945732.1:n.983T>C
XR_945733.1:n.920T>C
NM_000043.5:c.915T>C	NP_000034.1:p.Thr305=
NM_001320619.1:c.*238T>C	NP_001307548.1:n.*238T>C
NM_152871.3:c.852T>C	NP_690610.1:p.Thr284=
NM_152872.3:c.*227T>C	NP_690611.1:n.*227T>C
NR_028033.3:n.1061T>C
NR_028034.3:n.923T>C
NR_028035.3:n.986T>C
NR_028036.3:n.1124T>C
NR_135313.1:n.1041T>C
NR_135314.1:n.1224T>C
NR_135315.1:n.977T>C
XM_006717819.3:c.996T>C	XP_006717882.1:p.Thr332=
XM_011539764.2:c.1077T>C	XP_011538066.1:p.Thr359=
XM_011539765.2:c.1014T>C	XP_011538067.1:p.Thr338=
XM_011539766.2:c.996T>C	XP_011538068.1:p.Thr332=
XM_011539767.3:c.960T>C	XP_011538069.1:p.Thr320=
XR_945732.3:n.983T>C
XR_945733.2:n.920T>C
NM_000043.6:c.915T>C MANE Select	NP_000034.1:p.Thr305=
NM_001320619.2:c.*238T>C	NP_001307548.1:n.*238T>C
NM_152871.4:c.852T>C	NP_690610.1:p.Thr284=
NM_152872.4:c.*227T>C	NP_690611.1:n.*227T>C
NR_028033.4:n.822T>C
NR_028034.4:n.684T>C
NR_028035.4:n.747T>C
NR_028036.4:n.885T>C
NR_135313.2:n.802T>C
NR_135314.2:n.1081T>C
NR_135315.2:n.834T>C