Canonical Allele Identifier: CA5593252

Gene: FAS

Linked Data

• dbSNP Id: rs190852915
• ExAC: 10:90774250 G / A
• gnomAD v2: 10-90774250-G-A
• gnomAD v3: 10-89014493-G-A
• gnomAD v4: 10-89014493-G-A
• MyVariant Identifiers: chr10:g.90774250G>A (hg19) ; chr10:g.89014493G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014493G>A , CM000672.2:g.89014493G>A	GRCh38
NC_000010.10:g.90774250G>A , CM000672.1:g.90774250G>A	GRCh37
NC_000010.9:g.90764230G>A	NCBI36
NG_009089.2:g.28963G>A , LRG_134:g.28963G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1360G>A
ENST00000355740.8:c.*374G>A	ENSP00000347979.3:n.*374G>A
ENST00000357339.7:c.*43G>A	ENSP00000349896.2:n.*43G>A
ENST00000371857.8:n.2596G>A
ENST00000460510.6:c.*43G>A	ENSP00000512812.1:n.*43G>A
ENST00000466081.6:n.2700G>A
ENST00000477270.6:c.*43G>A	ENSP00000512813.1:n.*43G>A
ENST00000479522.6:c.*480G>A	ENSP00000424113.1:n.*480G>A
ENST00000484444.6:c.*492G>A	ENSP00000420975.1:n.*492G>A
ENST00000488877.6:c.942G>A	ENSP00000425159.1:n.942G>A
ENST00000492756.7:c.*480G>A	ENSP00000422453.1:n.*480G>A
ENST00000494799.6:c.*43G>A	ENSP00000512834.1:n.*43G>A
ENST00000562983.3:c.*43G>A	ENSP00000512845.1:n.*43G>A
ENST00000612663.6:c.*453G>A	ENSP00000477997.3:n.*453G>A
ENST00000640140.2:n.1196G>A
ENST00000640250.2:n.550G>A
ENST00000640681.2:n.1155G>A
ENST00000696723.1:n.4684G>A
ENST00000696741.1:n.2689G>A
ENST00000696742.1:n.2416G>A
ENST00000696743.1:n.3819G>A
ENST00000696744.1:n.1090G>A
ENST00000696767.1:n.1385G>A
ENST00000696768.1:c.*374G>A	ENSP00000512859.1:n.*374G>A
ENST00000696769.1:n.2740G>A
ENST00000696771.1:c.*43G>A	ENSP00000512860.1:n.*43G>A
ENST00000696772.1:n.2654G>A
ENST00000696773.1:n.2393G>A
ENST00000696774.1:n.6161G>A
ENST00000696776.1:c.*43G>A	ENSP00000512861.1:n.*43G>A
ENST00000696777.1:n.2459G>A
ENST00000696778.1:n.1487G>A
ENST00000696779.1:c.*43G>A	ENSP00000512862.1:n.*43G>A
ENST00000696780.1:c.*43G>A	ENSP00000512863.1:n.*43G>A
ENST00000696781.1:c.*43G>A	ENSP00000512864.1:n.*43G>A
ENST00000696782.1:c.*453G>A	ENSP00000512865.1:n.*453G>A
ENST00000696783.1:n.2919G>A
ENST00000696992.1:n.2168G>A
ENST00000696995.1:n.4580G>A
ENST00000696996.1:n.2493G>A
ENST00000696997.1:c.*681G>A	ENSP00000513028.1:n.*681G>A
ENST00000696998.1:n.2305G>A
ENST00000696999.1:c.*43G>A	ENSP00000513029.1:n.*43G>A
ENST00000697036.1:c.*467G>A	ENSP00000513060.1:n.*467G>A
ENST00000697037.1:n.1086G>A
ENST00000697093.1:n.3287G>A
ENST00000697094.1:n.3634G>A
ENST00000697095.1:c.*2252G>A	ENSP00000513104.1:n.*2252G>A
ENST00000697096.1:n.2184G>A
ENST00000697097.1:c.*43G>A	ENSP00000513105.1:n.*43G>A
ENST00000562983.2:n.1237G>A
ENST00000690268.1:c.*43G>A	ENSP00000509810.1:n.*43G>A
ENST00000355740.7:c.*377G>A	ENSP00000347979.3:n.*377G>A
ENST00000640140.1:n.1223G>A
ENST00000640250.1:n.550G>A
ENST00000640681.1:n.1172G>A
ENST00000652046.1:c.*43G>A MANE Select	ENSP00000498466.1:n.*43G>A
ENST00000352159.8:c.*368G>A	ENSP00000345601.4:n.*368G>A
ENST00000355740.6:c.*43G>A	ENSP00000347979.2:n.*43G>A
ENST00000479522.5:c.*480G>A	ENSP00000424113.1:n.*480G>A
ENST00000484444.5:c.*492G>A	ENSP00000420975.1:n.*492G>A
ENST00000494410.5:c.*409G>A	ENSP00000423755.1:n.*409G>A
NM_000043.4:c.*43G>A , LRG_134t1:c.*43G>A	NP_000034.1:n.*43G>A
NM_152871.2:c.*43G>A	NP_690610.1:n.*43G>A
NM_152872.2:c.*363G>A	NP_690611.1:n.*363G>A
NR_028033.2:n.1225G>A
NR_028034.2:n.1087G>A
NR_028035.2:n.1150G>A
NR_028036.2:n.1288G>A
XM_006717819.2:c.*43G>A	XP_006717882.1:n.*43G>A
XM_011539764.1:c.*43G>A	XP_011538066.1:n.*43G>A
XM_011539765.1:c.*43G>A	XP_011538067.1:n.*43G>A
XM_011539766.1:c.*43G>A	XP_011538068.1:n.*43G>A
XM_011539767.1:c.*43G>A	XP_011538069.1:n.*43G>A
XR_945733.1:n.1056G>A
NM_000043.5:c.*43G>A	NP_000034.1:n.*43G>A
NM_001320619.1:c.*374G>A	NP_001307548.1:n.*374G>A
NM_152871.3:c.*43G>A	NP_690610.1:n.*43G>A
NM_152872.3:c.*363G>A	NP_690611.1:n.*363G>A
NR_028033.3:n.1197G>A
NR_028034.3:n.1059G>A
NR_028035.3:n.1122G>A
NR_028036.3:n.1260G>A
NR_135313.1:n.1177G>A
NR_135314.1:n.1360G>A
NR_135315.1:n.1113G>A
XM_006717819.3:c.*43G>A	XP_006717882.1:n.*43G>A
XM_011539764.2:c.*43G>A	XP_011538066.1:n.*43G>A
XM_011539765.2:c.*43G>A	XP_011538067.1:n.*43G>A
XM_011539766.2:c.*43G>A	XP_011538068.1:n.*43G>A
XM_011539767.3:c.*43G>A	XP_011538069.1:n.*43G>A
XR_945732.3:n.1119G>A
XR_945733.2:n.1056G>A
NM_000043.6:c.*43G>A MANE Select	NP_000034.1:n.*43G>A
NM_001320619.2:c.*374G>A	NP_001307548.1:n.*374G>A
NM_152871.4:c.*43G>A	NP_690610.1:n.*43G>A
NM_152872.4:c.*363G>A	NP_690611.1:n.*363G>A
NR_028033.4:n.958G>A
NR_028034.4:n.820G>A
NR_028035.4:n.883G>A
NR_028036.4:n.1021G>A
NR_135313.2:n.938G>A
NR_135314.2:n.1217G>A
NR_135315.2:n.970G>A