Canonical Allele Identifier: CA930982963

Gene: FAS

Linked Data

• dbSNP Id: rs1848698231
• gnomAD v3: 10-89014550-A-C
• gnomAD v4: 10-89014550-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014550A>C , CM000672.2:g.89014550A>C	GRCh38
NC_000010.10:g.90774307A>C , CM000672.1:g.90774307A>C	GRCh37
NC_000010.9:g.90764287A>C	NCBI36
NG_009089.2:g.29020A>C , LRG_134:g.29020A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1417A>C
ENST00000355740.8:c.*431A>C	ENSP00000347979.3:n.*431A>C
ENST00000357339.7:c.*100A>C	ENSP00000349896.2:n.*100A>C
ENST00000371857.8:n.2653A>C
ENST00000460510.6:c.*100A>C	ENSP00000512812.1:n.*100A>C
ENST00000466081.6:n.2757A>C
ENST00000477270.6:c.*100A>C	ENSP00000512813.1:n.*100A>C
ENST00000479522.6:c.*537A>C	ENSP00000424113.1:n.*537A>C
ENST00000484444.6:c.*549A>C	ENSP00000420975.1:n.*549A>C
ENST00000488877.6:c.999A>C	ENSP00000425159.1:n.999A>C
ENST00000492756.7:c.*537A>C	ENSP00000422453.1:n.*537A>C
ENST00000494799.6:c.*100A>C	ENSP00000512834.1:n.*100A>C
ENST00000562983.3:c.*100A>C	ENSP00000512845.1:n.*100A>C
ENST00000612663.6:c.*510A>C	ENSP00000477997.3:n.*510A>C
ENST00000640140.2:n.1253A>C
ENST00000640250.2:n.607A>C
ENST00000640681.2:n.1212A>C
ENST00000696723.1:n.4741A>C
ENST00000696741.1:n.2746A>C
ENST00000696742.1:n.2473A>C
ENST00000696743.1:n.3876A>C
ENST00000696744.1:n.1147A>C
ENST00000696767.1:n.1442A>C
ENST00000696768.1:c.*431A>C	ENSP00000512859.1:n.*431A>C
ENST00000696769.1:n.2797A>C
ENST00000696771.1:c.*100A>C	ENSP00000512860.1:n.*100A>C
ENST00000696772.1:n.2711A>C
ENST00000696773.1:n.2450A>C
ENST00000696774.1:n.6218A>C
ENST00000696776.1:c.*100A>C	ENSP00000512861.1:n.*100A>C
ENST00000696777.1:n.2516A>C
ENST00000696778.1:n.1544A>C
ENST00000696779.1:c.*100A>C	ENSP00000512862.1:n.*100A>C
ENST00000696780.1:c.*100A>C	ENSP00000512863.1:n.*100A>C
ENST00000696781.1:c.*100A>C	ENSP00000512864.1:n.*100A>C
ENST00000696782.1:c.*510A>C	ENSP00000512865.1:n.*510A>C
ENST00000696783.1:n.2976A>C
ENST00000696992.1:n.2225A>C
ENST00000696995.1:n.4637A>C
ENST00000696996.1:n.2550A>C
ENST00000696997.1:c.*738A>C	ENSP00000513028.1:n.*738A>C
ENST00000696998.1:n.2362A>C
ENST00000696999.1:c.*100A>C	ENSP00000513029.1:n.*100A>C
ENST00000697036.1:c.*524A>C	ENSP00000513060.1:n.*524A>C
ENST00000697037.1:n.1143A>C
ENST00000697093.1:n.3344A>C
ENST00000697094.1:n.3691A>C
ENST00000697095.1:c.*2309A>C	ENSP00000513104.1:n.*2309A>C
ENST00000697096.1:n.2241A>C
ENST00000697097.1:c.*100A>C	ENSP00000513105.1:n.*100A>C
ENST00000562983.2:n.1294A>C
ENST00000690268.1:c.*100A>C	ENSP00000509810.1:n.*100A>C
ENST00000355740.7:c.*434A>C	ENSP00000347979.3:n.*434A>C
ENST00000640140.1:n.1280A>C
ENST00000640250.1:n.607A>C
ENST00000640681.1:n.1229A>C
ENST00000652046.1:c.*100A>C MANE Select	ENSP00000498466.1:n.*100A>C
ENST00000352159.8:c.*425A>C	ENSP00000345601.4:n.*425A>C
ENST00000355740.6:c.*100A>C	ENSP00000347979.2:n.*100A>C
ENST00000479522.5:c.*537A>C	ENSP00000424113.1:n.*537A>C
ENST00000484444.5:c.*549A>C	ENSP00000420975.1:n.*549A>C
ENST00000494410.5:c.*466A>C	ENSP00000423755.1:n.*466A>C
NM_000043.4:c.*100A>C , LRG_134t1:c.*100A>C	NP_000034.1:n.*100A>C
NM_152871.2:c.*100A>C	NP_690610.1:n.*100A>C
NM_152872.2:c.*420A>C	NP_690611.1:n.*420A>C
NR_028033.2:n.1282A>C
NR_028034.2:n.1144A>C
NR_028035.2:n.1207A>C
NR_028036.2:n.1345A>C
XM_006717819.2:c.*100A>C	XP_006717882.1:n.*100A>C
XM_011539764.1:c.*100A>C	XP_011538066.1:n.*100A>C
XM_011539765.1:c.*100A>C	XP_011538067.1:n.*100A>C
XM_011539766.1:c.*100A>C	XP_011538068.1:n.*100A>C
XM_011539767.1:c.*100A>C	XP_011538069.1:n.*100A>C
NM_000043.5:c.*100A>C	NP_000034.1:n.*100A>C
NM_001320619.1:c.*431A>C	NP_001307548.1:n.*431A>C
NM_152871.3:c.*100A>C	NP_690610.1:n.*100A>C
NM_152872.3:c.*420A>C	NP_690611.1:n.*420A>C
NR_028033.3:n.1254A>C
NR_028034.3:n.1116A>C
NR_028035.3:n.1179A>C
NR_028036.3:n.1317A>C
NR_135313.1:n.1234A>C
NR_135314.1:n.1417A>C
NR_135315.1:n.1170A>C
XM_006717819.3:c.*100A>C	XP_006717882.1:n.*100A>C
XM_011539764.2:c.*100A>C	XP_011538066.1:n.*100A>C
XM_011539765.2:c.*100A>C	XP_011538067.1:n.*100A>C
XM_011539766.2:c.*100A>C	XP_011538068.1:n.*100A>C
XM_011539767.3:c.*100A>C	XP_011538069.1:n.*100A>C
XR_945732.3:n.1176A>C
XR_945733.2:n.1113A>C
NM_000043.6:c.*100A>C MANE Select	NP_000034.1:n.*100A>C
NM_001320619.2:c.*431A>C	NP_001307548.1:n.*431A>C
NM_152871.4:c.*100A>C	NP_690610.1:n.*100A>C
NM_152872.4:c.*420A>C	NP_690611.1:n.*420A>C
NR_028033.4:n.1015A>C
NR_028034.4:n.877A>C
NR_028035.4:n.940A>C
NR_028036.4:n.1078A>C
NR_135313.2:n.995A>C
NR_135314.2:n.1274A>C
NR_135315.2:n.1027A>C