Canonical Allele Identifier: CA595185137

Gene: FAS

Linked Data

• dbSNP Id: rs1333319367
• gnomAD v2: 10-90774284-C-A
• gnomAD v4: 10-89014527-C-A
• MyVariant Identifiers: chr10:g.90774284C>A (hg19) ; chr10:g.89014527C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014527C>A , CM000672.2:g.89014527C>A	GRCh38
NC_000010.10:g.90774284C>A , CM000672.1:g.90774284C>A	GRCh37
NC_000010.9:g.90764264C>A	NCBI36
NG_009089.2:g.28997C>A , LRG_134:g.28997C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1394C>A
ENST00000355740.8:c.*408C>A	ENSP00000347979.3:n.*408C>A
ENST00000357339.7:c.*77C>A	ENSP00000349896.2:n.*77C>A
ENST00000371857.8:n.2630C>A
ENST00000460510.6:c.*77C>A	ENSP00000512812.1:n.*77C>A
ENST00000466081.6:n.2734C>A
ENST00000477270.6:c.*77C>A	ENSP00000512813.1:n.*77C>A
ENST00000479522.6:c.*514C>A	ENSP00000424113.1:n.*514C>A
ENST00000484444.6:c.*526C>A	ENSP00000420975.1:n.*526C>A
ENST00000488877.6:c.976C>A	ENSP00000425159.1:n.976C>A
ENST00000492756.7:c.*514C>A	ENSP00000422453.1:n.*514C>A
ENST00000494799.6:c.*77C>A	ENSP00000512834.1:n.*77C>A
ENST00000562983.3:c.*77C>A	ENSP00000512845.1:n.*77C>A
ENST00000612663.6:c.*487C>A	ENSP00000477997.3:n.*487C>A
ENST00000640140.2:n.1230C>A
ENST00000640250.2:n.584C>A
ENST00000640681.2:n.1189C>A
ENST00000696723.1:n.4718C>A
ENST00000696741.1:n.2723C>A
ENST00000696742.1:n.2450C>A
ENST00000696743.1:n.3853C>A
ENST00000696744.1:n.1124C>A
ENST00000696767.1:n.1419C>A
ENST00000696768.1:c.*408C>A	ENSP00000512859.1:n.*408C>A
ENST00000696769.1:n.2774C>A
ENST00000696771.1:c.*77C>A	ENSP00000512860.1:n.*77C>A
ENST00000696772.1:n.2688C>A
ENST00000696773.1:n.2427C>A
ENST00000696774.1:n.6195C>A
ENST00000696776.1:c.*77C>A	ENSP00000512861.1:n.*77C>A
ENST00000696777.1:n.2493C>A
ENST00000696778.1:n.1521C>A
ENST00000696779.1:c.*77C>A	ENSP00000512862.1:n.*77C>A
ENST00000696780.1:c.*77C>A	ENSP00000512863.1:n.*77C>A
ENST00000696781.1:c.*77C>A	ENSP00000512864.1:n.*77C>A
ENST00000696782.1:c.*487C>A	ENSP00000512865.1:n.*487C>A
ENST00000696783.1:n.2953C>A
ENST00000696992.1:n.2202C>A
ENST00000696995.1:n.4614C>A
ENST00000696996.1:n.2527C>A
ENST00000696997.1:c.*715C>A	ENSP00000513028.1:n.*715C>A
ENST00000696998.1:n.2339C>A
ENST00000696999.1:c.*77C>A	ENSP00000513029.1:n.*77C>A
ENST00000697036.1:c.*501C>A	ENSP00000513060.1:n.*501C>A
ENST00000697037.1:n.1120C>A
ENST00000697093.1:n.3321C>A
ENST00000697094.1:n.3668C>A
ENST00000697095.1:c.*2286C>A	ENSP00000513104.1:n.*2286C>A
ENST00000697096.1:n.2218C>A
ENST00000697097.1:c.*77C>A	ENSP00000513105.1:n.*77C>A
ENST00000562983.2:n.1271C>A
ENST00000690268.1:c.*77C>A	ENSP00000509810.1:n.*77C>A
ENST00000355740.7:c.*411C>A	ENSP00000347979.3:n.*411C>A
ENST00000640140.1:n.1257C>A
ENST00000640250.1:n.584C>A
ENST00000640681.1:n.1206C>A
ENST00000652046.1:c.*77C>A MANE Select	ENSP00000498466.1:n.*77C>A
ENST00000352159.8:c.*402C>A	ENSP00000345601.4:n.*402C>A
ENST00000355740.6:c.*77C>A	ENSP00000347979.2:n.*77C>A
ENST00000479522.5:c.*514C>A	ENSP00000424113.1:n.*514C>A
ENST00000484444.5:c.*526C>A	ENSP00000420975.1:n.*526C>A
ENST00000494410.5:c.*443C>A	ENSP00000423755.1:n.*443C>A
NM_000043.4:c.*77C>A , LRG_134t1:c.*77C>A	NP_000034.1:n.*77C>A
NM_152871.2:c.*77C>A	NP_690610.1:n.*77C>A
NM_152872.2:c.*397C>A	NP_690611.1:n.*397C>A
NR_028033.2:n.1259C>A
NR_028034.2:n.1121C>A
NR_028035.2:n.1184C>A
NR_028036.2:n.1322C>A
XM_006717819.2:c.*77C>A	XP_006717882.1:n.*77C>A
XM_011539764.1:c.*77C>A	XP_011538066.1:n.*77C>A
XM_011539765.1:c.*77C>A	XP_011538067.1:n.*77C>A
XM_011539766.1:c.*77C>A	XP_011538068.1:n.*77C>A
XM_011539767.1:c.*77C>A	XP_011538069.1:n.*77C>A
NM_000043.5:c.*77C>A	NP_000034.1:n.*77C>A
NM_001320619.1:c.*408C>A	NP_001307548.1:n.*408C>A
NM_152871.3:c.*77C>A	NP_690610.1:n.*77C>A
NM_152872.3:c.*397C>A	NP_690611.1:n.*397C>A
NR_028033.3:n.1231C>A
NR_028034.3:n.1093C>A
NR_028035.3:n.1156C>A
NR_028036.3:n.1294C>A
NR_135313.1:n.1211C>A
NR_135314.1:n.1394C>A
NR_135315.1:n.1147C>A
XM_006717819.3:c.*77C>A	XP_006717882.1:n.*77C>A
XM_011539764.2:c.*77C>A	XP_011538066.1:n.*77C>A
XM_011539765.2:c.*77C>A	XP_011538067.1:n.*77C>A
XM_011539766.2:c.*77C>A	XP_011538068.1:n.*77C>A
XM_011539767.3:c.*77C>A	XP_011538069.1:n.*77C>A
XR_945732.3:n.1153C>A
XR_945733.2:n.1090C>A
NM_000043.6:c.*77C>A MANE Select	NP_000034.1:n.*77C>A
NM_001320619.2:c.*408C>A	NP_001307548.1:n.*408C>A
NM_152871.4:c.*77C>A	NP_690610.1:n.*77C>A
NM_152872.4:c.*397C>A	NP_690611.1:n.*397C>A
NR_028033.4:n.992C>A
NR_028034.4:n.854C>A
NR_028035.4:n.917C>A
NR_028036.4:n.1055C>A
NR_135313.2:n.972C>A
NR_135314.2:n.1251C>A
NR_135315.2:n.1004C>A