Canonical Allele Identifier: CA5593259

Gene: FAS

Linked Data

• ClinVar Variation Id: 301532
• ClinVar RCV Id: RCV000407837
• dbSNP Id: rs754986111
• ExAC: 10:90774291 G / A
• gnomAD v2: 10-90774291-G-A
• gnomAD v3: 10-89014534-G-A
• gnomAD v4: 10-89014534-G-A
• MyVariant Identifiers: chr10:g.90774291G>A (hg19) ; chr10:g.89014534G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014534G>A , CM000672.2:g.89014534G>A	GRCh38
NC_000010.10:g.90774291G>A , CM000672.1:g.90774291G>A	GRCh37
NC_000010.9:g.90764271G>A	NCBI36
NG_009089.2:g.29004G>A , LRG_134:g.29004G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1401G>A
ENST00000355740.8:c.*415G>A	ENSP00000347979.3:n.*415G>A
ENST00000357339.7:c.*84G>A	ENSP00000349896.2:n.*84G>A
ENST00000371857.8:n.2637G>A
ENST00000460510.6:c.*84G>A	ENSP00000512812.1:n.*84G>A
ENST00000466081.6:n.2741G>A
ENST00000477270.6:c.*84G>A	ENSP00000512813.1:n.*84G>A
ENST00000479522.6:c.*521G>A	ENSP00000424113.1:n.*521G>A
ENST00000484444.6:c.*533G>A	ENSP00000420975.1:n.*533G>A
ENST00000488877.6:c.983G>A	ENSP00000425159.1:n.983G>A
ENST00000492756.7:c.*521G>A	ENSP00000422453.1:n.*521G>A
ENST00000494799.6:c.*84G>A	ENSP00000512834.1:n.*84G>A
ENST00000562983.3:c.*84G>A	ENSP00000512845.1:n.*84G>A
ENST00000612663.6:c.*494G>A	ENSP00000477997.3:n.*494G>A
ENST00000640140.2:n.1237G>A
ENST00000640250.2:n.591G>A
ENST00000640681.2:n.1196G>A
ENST00000696723.1:n.4725G>A
ENST00000696741.1:n.2730G>A
ENST00000696742.1:n.2457G>A
ENST00000696743.1:n.3860G>A
ENST00000696744.1:n.1131G>A
ENST00000696767.1:n.1426G>A
ENST00000696768.1:c.*415G>A	ENSP00000512859.1:n.*415G>A
ENST00000696769.1:n.2781G>A
ENST00000696771.1:c.*84G>A	ENSP00000512860.1:n.*84G>A
ENST00000696772.1:n.2695G>A
ENST00000696773.1:n.2434G>A
ENST00000696774.1:n.6202G>A
ENST00000696776.1:c.*84G>A	ENSP00000512861.1:n.*84G>A
ENST00000696777.1:n.2500G>A
ENST00000696778.1:n.1528G>A
ENST00000696779.1:c.*84G>A	ENSP00000512862.1:n.*84G>A
ENST00000696780.1:c.*84G>A	ENSP00000512863.1:n.*84G>A
ENST00000696781.1:c.*84G>A	ENSP00000512864.1:n.*84G>A
ENST00000696782.1:c.*494G>A	ENSP00000512865.1:n.*494G>A
ENST00000696783.1:n.2960G>A
ENST00000696992.1:n.2209G>A
ENST00000696995.1:n.4621G>A
ENST00000696996.1:n.2534G>A
ENST00000696997.1:c.*722G>A	ENSP00000513028.1:n.*722G>A
ENST00000696998.1:n.2346G>A
ENST00000696999.1:c.*84G>A	ENSP00000513029.1:n.*84G>A
ENST00000697036.1:c.*508G>A	ENSP00000513060.1:n.*508G>A
ENST00000697037.1:n.1127G>A
ENST00000697093.1:n.3328G>A
ENST00000697094.1:n.3675G>A
ENST00000697095.1:c.*2293G>A	ENSP00000513104.1:n.*2293G>A
ENST00000697096.1:n.2225G>A
ENST00000697097.1:c.*84G>A	ENSP00000513105.1:n.*84G>A
ENST00000562983.2:n.1278G>A
ENST00000690268.1:c.*84G>A	ENSP00000509810.1:n.*84G>A
ENST00000355740.7:c.*418G>A	ENSP00000347979.3:n.*418G>A
ENST00000640140.1:n.1264G>A
ENST00000640250.1:n.591G>A
ENST00000640681.1:n.1213G>A
ENST00000652046.1:c.*84G>A MANE Select	ENSP00000498466.1:n.*84G>A
ENST00000352159.8:c.*409G>A	ENSP00000345601.4:n.*409G>A
ENST00000355740.6:c.*84G>A	ENSP00000347979.2:n.*84G>A
ENST00000479522.5:c.*521G>A	ENSP00000424113.1:n.*521G>A
ENST00000484444.5:c.*533G>A	ENSP00000420975.1:n.*533G>A
ENST00000494410.5:c.*450G>A	ENSP00000423755.1:n.*450G>A
NM_000043.4:c.*84G>A , LRG_134t1:c.*84G>A	NP_000034.1:n.*84G>A
NM_152871.2:c.*84G>A	NP_690610.1:n.*84G>A
NM_152872.2:c.*404G>A	NP_690611.1:n.*404G>A
NR_028033.2:n.1266G>A
NR_028034.2:n.1128G>A
NR_028035.2:n.1191G>A
NR_028036.2:n.1329G>A
XM_006717819.2:c.*84G>A	XP_006717882.1:n.*84G>A
XM_011539764.1:c.*84G>A	XP_011538066.1:n.*84G>A
XM_011539765.1:c.*84G>A	XP_011538067.1:n.*84G>A
XM_011539766.1:c.*84G>A	XP_011538068.1:n.*84G>A
XM_011539767.1:c.*84G>A	XP_011538069.1:n.*84G>A
NM_000043.5:c.*84G>A	NP_000034.1:n.*84G>A
NM_001320619.1:c.*415G>A	NP_001307548.1:n.*415G>A
NM_152871.3:c.*84G>A	NP_690610.1:n.*84G>A
NM_152872.3:c.*404G>A	NP_690611.1:n.*404G>A
NR_028033.3:n.1238G>A
NR_028034.3:n.1100G>A
NR_028035.3:n.1163G>A
NR_028036.3:n.1301G>A
NR_135313.1:n.1218G>A
NR_135314.1:n.1401G>A
NR_135315.1:n.1154G>A
XM_006717819.3:c.*84G>A	XP_006717882.1:n.*84G>A
XM_011539764.2:c.*84G>A	XP_011538066.1:n.*84G>A
XM_011539765.2:c.*84G>A	XP_011538067.1:n.*84G>A
XM_011539766.2:c.*84G>A	XP_011538068.1:n.*84G>A
XM_011539767.3:c.*84G>A	XP_011538069.1:n.*84G>A
XR_945732.3:n.1160G>A
XR_945733.2:n.1097G>A
NM_000043.6:c.*84G>A MANE Select	NP_000034.1:n.*84G>A
NM_001320619.2:c.*415G>A	NP_001307548.1:n.*415G>A
NM_152871.4:c.*84G>A	NP_690610.1:n.*84G>A
NM_152872.4:c.*404G>A	NP_690611.1:n.*404G>A
NR_028033.4:n.999G>A
NR_028034.4:n.861G>A
NR_028035.4:n.924G>A
NR_028036.4:n.1062G>A
NR_135313.2:n.979G>A
NR_135314.2:n.1258G>A
NR_135315.2:n.1011G>A