Canonical Allele Identifier: CA5593257

Gene: FAS

Linked Data

• dbSNP Id: rs79014610
• ExAC: 10:90774279 A / T
• gnomAD v2: 10-90774279-A-T
• gnomAD v4: 10-89014522-A-T
• MyVariant Identifiers: chr10:g.90774279A>T (hg19) ; chr10:g.89014522A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014522A>T , CM000672.2:g.89014522A>T	GRCh38
NC_000010.10:g.90774279A>T , CM000672.1:g.90774279A>T	GRCh37
NC_000010.9:g.90764259A>T	NCBI36
NG_009089.2:g.28992A>T , LRG_134:g.28992A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1389A>T
ENST00000355740.8:c.*403A>T	ENSP00000347979.3:n.*403A>T
ENST00000357339.7:c.*72A>T	ENSP00000349896.2:n.*72A>T
ENST00000371857.8:n.2625A>T
ENST00000460510.6:c.*72A>T	ENSP00000512812.1:n.*72A>T
ENST00000466081.6:n.2729A>T
ENST00000477270.6:c.*72A>T	ENSP00000512813.1:n.*72A>T
ENST00000479522.6:c.*509A>T	ENSP00000424113.1:n.*509A>T
ENST00000484444.6:c.*521A>T	ENSP00000420975.1:n.*521A>T
ENST00000488877.6:c.971A>T	ENSP00000425159.1:n.971A>T
ENST00000492756.7:c.*509A>T	ENSP00000422453.1:n.*509A>T
ENST00000494799.6:c.*72A>T	ENSP00000512834.1:n.*72A>T
ENST00000562983.3:c.*72A>T	ENSP00000512845.1:n.*72A>T
ENST00000612663.6:c.*482A>T	ENSP00000477997.3:n.*482A>T
ENST00000640140.2:n.1225A>T
ENST00000640250.2:n.579A>T
ENST00000640681.2:n.1184A>T
ENST00000696723.1:n.4713A>T
ENST00000696741.1:n.2718A>T
ENST00000696742.1:n.2445A>T
ENST00000696743.1:n.3848A>T
ENST00000696744.1:n.1119A>T
ENST00000696767.1:n.1414A>T
ENST00000696768.1:c.*403A>T	ENSP00000512859.1:n.*403A>T
ENST00000696769.1:n.2769A>T
ENST00000696771.1:c.*72A>T	ENSP00000512860.1:n.*72A>T
ENST00000696772.1:n.2683A>T
ENST00000696773.1:n.2422A>T
ENST00000696774.1:n.6190A>T
ENST00000696776.1:c.*72A>T	ENSP00000512861.1:n.*72A>T
ENST00000696777.1:n.2488A>T
ENST00000696778.1:n.1516A>T
ENST00000696779.1:c.*72A>T	ENSP00000512862.1:n.*72A>T
ENST00000696780.1:c.*72A>T	ENSP00000512863.1:n.*72A>T
ENST00000696781.1:c.*72A>T	ENSP00000512864.1:n.*72A>T
ENST00000696782.1:c.*482A>T	ENSP00000512865.1:n.*482A>T
ENST00000696783.1:n.2948A>T
ENST00000696992.1:n.2197A>T
ENST00000696995.1:n.4609A>T
ENST00000696996.1:n.2522A>T
ENST00000696997.1:c.*710A>T	ENSP00000513028.1:n.*710A>T
ENST00000696998.1:n.2334A>T
ENST00000696999.1:c.*72A>T	ENSP00000513029.1:n.*72A>T
ENST00000697036.1:c.*496A>T	ENSP00000513060.1:n.*496A>T
ENST00000697037.1:n.1115A>T
ENST00000697093.1:n.3316A>T
ENST00000697094.1:n.3663A>T
ENST00000697095.1:c.*2281A>T	ENSP00000513104.1:n.*2281A>T
ENST00000697096.1:n.2213A>T
ENST00000697097.1:c.*72A>T	ENSP00000513105.1:n.*72A>T
ENST00000562983.2:n.1266A>T
ENST00000690268.1:c.*72A>T	ENSP00000509810.1:n.*72A>T
ENST00000355740.7:c.*406A>T	ENSP00000347979.3:n.*406A>T
ENST00000640140.1:n.1252A>T
ENST00000640250.1:n.579A>T
ENST00000640681.1:n.1201A>T
ENST00000652046.1:c.*72A>T MANE Select	ENSP00000498466.1:n.*72A>T
ENST00000352159.8:c.*397A>T	ENSP00000345601.4:n.*397A>T
ENST00000355740.6:c.*72A>T	ENSP00000347979.2:n.*72A>T
ENST00000479522.5:c.*509A>T	ENSP00000424113.1:n.*509A>T
ENST00000484444.5:c.*521A>T	ENSP00000420975.1:n.*521A>T
ENST00000494410.5:c.*438A>T	ENSP00000423755.1:n.*438A>T
NM_000043.4:c.*72A>T , LRG_134t1:c.*72A>T	NP_000034.1:n.*72A>T
NM_152871.2:c.*72A>T	NP_690610.1:n.*72A>T
NM_152872.2:c.*392A>T	NP_690611.1:n.*392A>T
NR_028033.2:n.1254A>T
NR_028034.2:n.1116A>T
NR_028035.2:n.1179A>T
NR_028036.2:n.1317A>T
XM_006717819.2:c.*72A>T	XP_006717882.1:n.*72A>T
XM_011539764.1:c.*72A>T	XP_011538066.1:n.*72A>T
XM_011539765.1:c.*72A>T	XP_011538067.1:n.*72A>T
XM_011539766.1:c.*72A>T	XP_011538068.1:n.*72A>T
XM_011539767.1:c.*72A>T	XP_011538069.1:n.*72A>T
NM_000043.5:c.*72A>T	NP_000034.1:n.*72A>T
NM_001320619.1:c.*403A>T	NP_001307548.1:n.*403A>T
NM_152871.3:c.*72A>T	NP_690610.1:n.*72A>T
NM_152872.3:c.*392A>T	NP_690611.1:n.*392A>T
NR_028033.3:n.1226A>T
NR_028034.3:n.1088A>T
NR_028035.3:n.1151A>T
NR_028036.3:n.1289A>T
NR_135313.1:n.1206A>T
NR_135314.1:n.1389A>T
NR_135315.1:n.1142A>T
XM_006717819.3:c.*72A>T	XP_006717882.1:n.*72A>T
XM_011539764.2:c.*72A>T	XP_011538066.1:n.*72A>T
XM_011539765.2:c.*72A>T	XP_011538067.1:n.*72A>T
XM_011539766.2:c.*72A>T	XP_011538068.1:n.*72A>T
XM_011539767.3:c.*72A>T	XP_011538069.1:n.*72A>T
XR_945732.3:n.1148A>T
XR_945733.2:n.1085A>T
NM_000043.6:c.*72A>T MANE Select	NP_000034.1:n.*72A>T
NM_001320619.2:c.*403A>T	NP_001307548.1:n.*403A>T
NM_152871.4:c.*72A>T	NP_690610.1:n.*72A>T
NM_152872.4:c.*392A>T	NP_690611.1:n.*392A>T
NR_028033.4:n.987A>T
NR_028034.4:n.849A>T
NR_028035.4:n.912A>T
NR_028036.4:n.1050A>T
NR_135313.2:n.967A>T
NR_135314.2:n.1246A>T
NR_135315.2:n.999A>T