Canonical Allele Identifier: CA470974934

Gene: FAS

Linked Data

• dbSNP Id: rs967060461
• gnomAD v3: 10-89014351-T-G
• gnomAD v4: 10-89014351-T-G
• MyVariant Identifiers: chr10:g.90774108T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014351T>G , CM000672.2:g.89014351T>G	GRCh38
NC_000010.10:g.90774108T>G , CM000672.1:g.90774108T>G	GRCh37
NC_000010.9:g.90764088T>G	NCBI36
NG_009089.2:g.28821T>G , LRG_134:g.28821T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1218T>G
ENST00000355740.8:c.*232T>G	ENSP00000347979.3:n.*232T>G
ENST00000357339.7:c.846T>G	ENSP00000349896.2:p.Leu282=
ENST00000371857.8:n.2454T>G
ENST00000460510.6:c.192T>G	ENSP00000512812.1:p.Leu64=
ENST00000466081.6:n.2558T>G
ENST00000477270.6:c.954T>G	ENSP00000512813.1:p.Leu318=
ENST00000479522.6:c.*338T>G	ENSP00000424113.1:n.*338T>G
ENST00000484444.6:c.*350T>G	ENSP00000420975.1:n.*350T>G
ENST00000488877.6:c.800T>G	ENSP00000425159.1:n.800T>G
ENST00000492756.7:c.*338T>G	ENSP00000422453.1:n.*338T>G
ENST00000494799.6:c.192T>G	ENSP00000512834.1:p.Leu64=
ENST00000562983.3:c.192T>G	ENSP00000512845.1:p.Leu64=
ENST00000612663.6:c.*311T>G	ENSP00000477997.3:n.*311T>G
ENST00000640140.2:n.1054T>G
ENST00000640250.2:n.408T>G
ENST00000640681.2:n.1013T>G
ENST00000696723.1:n.4542T>G
ENST00000696741.1:n.2547T>G
ENST00000696742.1:n.2274T>G
ENST00000696743.1:n.3677T>G
ENST00000696744.1:n.948T>G
ENST00000696767.1:n.1243T>G
ENST00000696768.1:c.*232T>G	ENSP00000512859.1:n.*232T>G
ENST00000696769.1:n.2598T>G
ENST00000696771.1:c.192T>G	ENSP00000512860.1:p.Leu64=
ENST00000696772.1:n.2512T>G
ENST00000696773.1:n.2251T>G
ENST00000696774.1:n.6019T>G
ENST00000696776.1:c.1002T>G	ENSP00000512861.1:p.Leu334=
ENST00000696777.1:n.2317T>G
ENST00000696778.1:n.1345T>G
ENST00000696779.1:c.516T>G	ENSP00000512862.1:p.Leu172=
ENST00000696780.1:c.939T>G	ENSP00000512863.1:p.Leu313=
ENST00000696781.1:c.654T>G	ENSP00000512864.1:p.Leu218=
ENST00000696782.1:c.*311T>G	ENSP00000512865.1:n.*311T>G
ENST00000696783.1:n.2777T>G
ENST00000696992.1:n.2026T>G
ENST00000696995.1:n.4438T>G
ENST00000696996.1:n.2351T>G
ENST00000696997.1:c.*539T>G	ENSP00000513028.1:n.*539T>G
ENST00000696998.1:n.2163T>G
ENST00000696999.1:c.192T>G	ENSP00000513029.1:p.Leu64=
ENST00000697036.1:c.*325T>G	ENSP00000513060.1:n.*325T>G
ENST00000697037.1:n.944T>G
ENST00000697093.1:n.3145T>G
ENST00000697094.1:n.3492T>G
ENST00000697095.1:c.*2110T>G	ENSP00000513104.1:n.*2110T>G
ENST00000697096.1:n.2042T>G
ENST00000697097.1:c.192T>G	ENSP00000513105.1:p.Leu64=
ENST00000562983.2:n.1095T>G
ENST00000690268.1:c.990T>G	ENSP00000509810.1:p.Leu330=
ENST00000355740.7:c.*235T>G	ENSP00000347979.3:n.*235T>G
ENST00000612663.5:c.*311T>G	ENSP00000477997.3:n.*311T>G
ENST00000640140.1:n.1081T>G
ENST00000640250.1:n.408T>G
ENST00000640681.1:n.1030T>G
ENST00000652046.1:c.909T>G MANE Select	ENSP00000498466.1:p.Leu303=
ENST00000352159.8:c.*226T>G	ENSP00000345601.4:n.*226T>G
ENST00000355279.2:c.884T>G	ENSP00000347426.2:n.884T>G
ENST00000355740.6:c.909T>G	ENSP00000347979.2:p.Leu303=
ENST00000357339.6:c.846T>G	ENSP00000349896.2:p.Leu282=
ENST00000479522.5:c.*338T>G	ENSP00000424113.1:n.*338T>G
ENST00000484444.5:c.*350T>G	ENSP00000420975.1:n.*350T>G
ENST00000488877.5:c.*350T>G	ENSP00000425159.1:n.*350T>G
ENST00000492756.5:c.737T>G	ENSP00000422453.1:n.737T>G
ENST00000494410.5:c.*267T>G	ENSP00000423755.1:n.*267T>G
ENST00000612663.4:c.*256T>G	ENSP00000477997.2:n.*256T>G
NM_000043.4:c.909T>G , LRG_134t1:c.909T>G	NP_000034.1:p.Leu303=
NM_152871.2:c.846T>G	NP_690610.1:p.Leu282=
NM_152872.2:c.*221T>G	NP_690611.1:n.*221T>G
NR_028033.2:n.1083T>G
NR_028034.2:n.945T>G
NR_028035.2:n.1008T>G
NR_028036.2:n.1146T>G
XM_006717819.2:c.990T>G	XP_006717882.1:p.Leu330=
XM_011539764.1:c.1071T>G	XP_011538066.1:p.Leu357=
XM_011539765.1:c.1008T>G	XP_011538067.1:p.Leu336=
XM_011539766.1:c.990T>G	XP_011538068.1:p.Leu330=
XM_011539767.1:c.954T>G	XP_011538069.1:p.Leu318=
XR_945732.1:n.977T>G
XR_945733.1:n.914T>G
NM_000043.5:c.909T>G	NP_000034.1:p.Leu303=
NM_001320619.1:c.*232T>G	NP_001307548.1:n.*232T>G
NM_152871.3:c.846T>G	NP_690610.1:p.Leu282=
NM_152872.3:c.*221T>G	NP_690611.1:n.*221T>G
NR_028033.3:n.1055T>G
NR_028034.3:n.917T>G
NR_028035.3:n.980T>G
NR_028036.3:n.1118T>G
NR_135313.1:n.1035T>G
NR_135314.1:n.1218T>G
NR_135315.1:n.971T>G
XM_006717819.3:c.990T>G	XP_006717882.1:p.Leu330=
XM_011539764.2:c.1071T>G	XP_011538066.1:p.Leu357=
XM_011539765.2:c.1008T>G	XP_011538067.1:p.Leu336=
XM_011539766.2:c.990T>G	XP_011538068.1:p.Leu330=
XM_011539767.3:c.954T>G	XP_011538069.1:p.Leu318=
XR_945732.3:n.977T>G
XR_945733.2:n.914T>G
NM_000043.6:c.909T>G MANE Select	NP_000034.1:p.Leu303=
NM_001320619.2:c.*232T>G	NP_001307548.1:n.*232T>G
NM_152871.4:c.846T>G	NP_690610.1:p.Leu282=
NM_152872.4:c.*221T>G	NP_690611.1:n.*221T>G
NR_028033.4:n.816T>G
NR_028034.4:n.678T>G
NR_028035.4:n.741T>G
NR_028036.4:n.879T>G
NR_135313.2:n.796T>G
NR_135314.2:n.1075T>G
NR_135315.2:n.828T>G