Canonical Allele Identifier: CA1926639545

Gene: FAS

Linked Data

• dbSNP Id: rs1848708837

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014699T>C , CM000672.2:g.89014699T>C	GRCh38
NC_000010.10:g.90774456T>C , CM000672.1:g.90774456T>C	GRCh37
NC_000010.9:g.90764436T>C	NCBI36
NG_009089.2:g.29169T>C , LRG_134:g.29169T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1566T>C
ENST00000355740.8:c.*580T>C	ENSP00000347979.3:n.*580T>C
ENST00000357339.7:c.*249T>C	ENSP00000349896.2:n.*249T>C
ENST00000371857.8:n.2802T>C
ENST00000460510.6:c.*249T>C	ENSP00000512812.1:n.*249T>C
ENST00000466081.6:n.2906T>C
ENST00000477270.6:c.*249T>C	ENSP00000512813.1:n.*249T>C
ENST00000492756.7:c.*686T>C	ENSP00000422453.1:n.*686T>C
ENST00000494799.6:c.*249T>C	ENSP00000512834.1:n.*249T>C
ENST00000562983.3:c.*249T>C	ENSP00000512845.1:n.*249T>C
ENST00000612663.6:c.*659T>C	ENSP00000477997.3:n.*659T>C
ENST00000640140.2:n.1402T>C
ENST00000640250.2:n.756T>C
ENST00000640681.2:n.1361T>C
ENST00000696723.1:n.4890T>C
ENST00000696741.1:n.2895T>C
ENST00000696742.1:n.2622T>C
ENST00000696743.1:n.4025T>C
ENST00000696744.1:n.1296T>C
ENST00000696767.1:n.1591T>C
ENST00000696768.1:c.*580T>C	ENSP00000512859.1:n.*580T>C
ENST00000696771.1:c.*249T>C	ENSP00000512860.1:n.*249T>C
ENST00000696772.1:n.2860T>C
ENST00000696773.1:n.2599T>C
ENST00000696774.1:n.6367T>C
ENST00000696776.1:c.*249T>C	ENSP00000512861.1:n.*249T>C
ENST00000696777.1:n.2665T>C
ENST00000696778.1:n.1693T>C
ENST00000696779.1:c.*249T>C	ENSP00000512862.1:n.*249T>C
ENST00000696780.1:c.*249T>C	ENSP00000512863.1:n.*249T>C
ENST00000696781.1:c.*249T>C	ENSP00000512864.1:n.*249T>C
ENST00000696782.1:c.*659T>C	ENSP00000512865.1:n.*659T>C
ENST00000696783.1:n.3125T>C
ENST00000696992.1:n.2374T>C
ENST00000696995.1:n.4786T>C
ENST00000696996.1:n.2699T>C
ENST00000696997.1:c.*887T>C	ENSP00000513028.1:n.*887T>C
ENST00000696998.1:n.2511T>C
ENST00000696999.1:c.*249T>C	ENSP00000513029.1:n.*249T>C
ENST00000697036.1:c.*673T>C	ENSP00000513060.1:n.*673T>C
ENST00000697037.1:n.1292T>C
ENST00000697093.1:n.3493T>C
ENST00000697094.1:n.3840T>C
ENST00000697095.1:c.*2458T>C	ENSP00000513104.1:n.*2458T>C
ENST00000697096.1:n.2390T>C
ENST00000697097.1:c.*249T>C	ENSP00000513105.1:n.*249T>C
ENST00000562983.2:n.1443T>C
ENST00000690268.1:c.*249T>C	ENSP00000509810.1:n.*249T>C
ENST00000355740.7:c.*583T>C	ENSP00000347979.3:n.*583T>C
ENST00000640140.1:n.1429T>C
ENST00000640250.1:n.756T>C
ENST00000640681.1:n.1378T>C
ENST00000652046.1:c.*249T>C MANE Select	ENSP00000498466.1:n.*249T>C
ENST00000352159.8:c.*574T>C	ENSP00000345601.4:n.*574T>C
ENST00000355740.6:c.*249T>C	ENSP00000347979.2:n.*249T>C
NM_000043.4:c.*249T>C , LRG_134t1:c.*249T>C	NP_000034.1:n.*249T>C
NM_152871.2:c.*249T>C	NP_690610.1:n.*249T>C
NM_152872.2:c.*569T>C	NP_690611.1:n.*569T>C
NR_028033.2:n.1431T>C
NR_028034.2:n.1293T>C
NR_028035.2:n.1356T>C
NR_028036.2:n.1494T>C
XM_006717819.2:c.*249T>C	XP_006717882.1:n.*249T>C
XM_011539764.1:c.*249T>C	XP_011538066.1:n.*249T>C
XM_011539765.1:c.*249T>C	XP_011538067.1:n.*249T>C
XM_011539766.1:c.*249T>C	XP_011538068.1:n.*249T>C
XM_011539767.1:c.*249T>C	XP_011538069.1:n.*249T>C
NM_000043.5:c.*249T>C	NP_000034.1:n.*249T>C
NM_001320619.1:c.*580T>C	NP_001307548.1:n.*580T>C
NM_152871.3:c.*249T>C	NP_690610.1:n.*249T>C
NM_152872.3:c.*569T>C	NP_690611.1:n.*569T>C
NR_028033.3:n.1403T>C
NR_028034.3:n.1265T>C
NR_028035.3:n.1328T>C
NR_028036.3:n.1466T>C
NR_135313.1:n.1383T>C
NR_135314.1:n.1566T>C
NR_135315.1:n.1319T>C
XM_006717819.3:c.*249T>C	XP_006717882.1:n.*249T>C
XM_011539764.2:c.*249T>C	XP_011538066.1:n.*249T>C
XM_011539765.2:c.*249T>C	XP_011538067.1:n.*249T>C
XM_011539766.2:c.*249T>C	XP_011538068.1:n.*249T>C
XM_011539767.3:c.*249T>C	XP_011538069.1:n.*249T>C
XR_945732.3:n.1325T>C
XR_945733.2:n.1262T>C
NM_000043.6:c.*249T>C MANE Select	NP_000034.1:n.*249T>C
NM_001320619.2:c.*580T>C	NP_001307548.1:n.*580T>C
NM_152871.4:c.*249T>C	NP_690610.1:n.*249T>C
NM_152872.4:c.*569T>C	NP_690611.1:n.*569T>C
NR_028033.4:n.1164T>C
NR_028034.4:n.1026T>C
NR_028035.4:n.1089T>C
NR_028036.4:n.1227T>C
NR_135313.2:n.1144T>C
NR_135314.2:n.1423T>C
NR_135315.2:n.1176T>C