Canonical Allele Identifier: CA5593255

Gene: FAS

Linked Data

• dbSNP Id: rs755243893
• ExAC: 10:90774273 G / A
• gnomAD v2: 10-90774273-G-A
• gnomAD v3: 10-89014516-G-A
• gnomAD v4: 10-89014516-G-A
• MyVariant Identifiers: chr10:g.90774273G>A (hg19) ; chr10:g.89014516G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014516G>A , CM000672.2:g.89014516G>A	GRCh38
NC_000010.10:g.90774273G>A , CM000672.1:g.90774273G>A	GRCh37
NC_000010.9:g.90764253G>A	NCBI36
NG_009089.2:g.28986G>A , LRG_134:g.28986G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1383G>A
ENST00000355740.8:c.*397G>A	ENSP00000347979.3:n.*397G>A
ENST00000357339.7:c.*66G>A	ENSP00000349896.2:n.*66G>A
ENST00000371857.8:n.2619G>A
ENST00000460510.6:c.*66G>A	ENSP00000512812.1:n.*66G>A
ENST00000466081.6:n.2723G>A
ENST00000477270.6:c.*66G>A	ENSP00000512813.1:n.*66G>A
ENST00000479522.6:c.*503G>A	ENSP00000424113.1:n.*503G>A
ENST00000484444.6:c.*515G>A	ENSP00000420975.1:n.*515G>A
ENST00000488877.6:c.965G>A	ENSP00000425159.1:n.965G>A
ENST00000492756.7:c.*503G>A	ENSP00000422453.1:n.*503G>A
ENST00000494799.6:c.*66G>A	ENSP00000512834.1:n.*66G>A
ENST00000562983.3:c.*66G>A	ENSP00000512845.1:n.*66G>A
ENST00000612663.6:c.*476G>A	ENSP00000477997.3:n.*476G>A
ENST00000640140.2:n.1219G>A
ENST00000640250.2:n.573G>A
ENST00000640681.2:n.1178G>A
ENST00000696723.1:n.4707G>A
ENST00000696741.1:n.2712G>A
ENST00000696742.1:n.2439G>A
ENST00000696743.1:n.3842G>A
ENST00000696744.1:n.1113G>A
ENST00000696767.1:n.1408G>A
ENST00000696768.1:c.*397G>A	ENSP00000512859.1:n.*397G>A
ENST00000696769.1:n.2763G>A
ENST00000696771.1:c.*66G>A	ENSP00000512860.1:n.*66G>A
ENST00000696772.1:n.2677G>A
ENST00000696773.1:n.2416G>A
ENST00000696774.1:n.6184G>A
ENST00000696776.1:c.*66G>A	ENSP00000512861.1:n.*66G>A
ENST00000696777.1:n.2482G>A
ENST00000696778.1:n.1510G>A
ENST00000696779.1:c.*66G>A	ENSP00000512862.1:n.*66G>A
ENST00000696780.1:c.*66G>A	ENSP00000512863.1:n.*66G>A
ENST00000696781.1:c.*66G>A	ENSP00000512864.1:n.*66G>A
ENST00000696782.1:c.*476G>A	ENSP00000512865.1:n.*476G>A
ENST00000696783.1:n.2942G>A
ENST00000696992.1:n.2191G>A
ENST00000696995.1:n.4603G>A
ENST00000696996.1:n.2516G>A
ENST00000696997.1:c.*704G>A	ENSP00000513028.1:n.*704G>A
ENST00000696998.1:n.2328G>A
ENST00000696999.1:c.*66G>A	ENSP00000513029.1:n.*66G>A
ENST00000697036.1:c.*490G>A	ENSP00000513060.1:n.*490G>A
ENST00000697037.1:n.1109G>A
ENST00000697093.1:n.3310G>A
ENST00000697094.1:n.3657G>A
ENST00000697095.1:c.*2275G>A	ENSP00000513104.1:n.*2275G>A
ENST00000697096.1:n.2207G>A
ENST00000697097.1:c.*66G>A	ENSP00000513105.1:n.*66G>A
ENST00000562983.2:n.1260G>A
ENST00000690268.1:c.*66G>A	ENSP00000509810.1:n.*66G>A
ENST00000355740.7:c.*400G>A	ENSP00000347979.3:n.*400G>A
ENST00000640140.1:n.1246G>A
ENST00000640250.1:n.573G>A
ENST00000640681.1:n.1195G>A
ENST00000652046.1:c.*66G>A MANE Select	ENSP00000498466.1:n.*66G>A
ENST00000352159.8:c.*391G>A	ENSP00000345601.4:n.*391G>A
ENST00000355740.6:c.*66G>A	ENSP00000347979.2:n.*66G>A
ENST00000479522.5:c.*503G>A	ENSP00000424113.1:n.*503G>A
ENST00000484444.5:c.*515G>A	ENSP00000420975.1:n.*515G>A
ENST00000494410.5:c.*432G>A	ENSP00000423755.1:n.*432G>A
NM_000043.4:c.*66G>A , LRG_134t1:c.*66G>A	NP_000034.1:n.*66G>A
NM_152871.2:c.*66G>A	NP_690610.1:n.*66G>A
NM_152872.2:c.*386G>A	NP_690611.1:n.*386G>A
NR_028033.2:n.1248G>A
NR_028034.2:n.1110G>A
NR_028035.2:n.1173G>A
NR_028036.2:n.1311G>A
XM_006717819.2:c.*66G>A	XP_006717882.1:n.*66G>A
XM_011539764.1:c.*66G>A	XP_011538066.1:n.*66G>A
XM_011539765.1:c.*66G>A	XP_011538067.1:n.*66G>A
XM_011539766.1:c.*66G>A	XP_011538068.1:n.*66G>A
XM_011539767.1:c.*66G>A	XP_011538069.1:n.*66G>A
NM_000043.5:c.*66G>A	NP_000034.1:n.*66G>A
NM_001320619.1:c.*397G>A	NP_001307548.1:n.*397G>A
NM_152871.3:c.*66G>A	NP_690610.1:n.*66G>A
NM_152872.3:c.*386G>A	NP_690611.1:n.*386G>A
NR_028033.3:n.1220G>A
NR_028034.3:n.1082G>A
NR_028035.3:n.1145G>A
NR_028036.3:n.1283G>A
NR_135313.1:n.1200G>A
NR_135314.1:n.1383G>A
NR_135315.1:n.1136G>A
XM_006717819.3:c.*66G>A	XP_006717882.1:n.*66G>A
XM_011539764.2:c.*66G>A	XP_011538066.1:n.*66G>A
XM_011539765.2:c.*66G>A	XP_011538067.1:n.*66G>A
XM_011539766.2:c.*66G>A	XP_011538068.1:n.*66G>A
XM_011539767.3:c.*66G>A	XP_011538069.1:n.*66G>A
XR_945732.3:n.1142G>A
XR_945733.2:n.1079G>A
NM_000043.6:c.*66G>A MANE Select	NP_000034.1:n.*66G>A
NM_001320619.2:c.*397G>A	NP_001307548.1:n.*397G>A
NM_152871.4:c.*66G>A	NP_690610.1:n.*66G>A
NM_152872.4:c.*386G>A	NP_690611.1:n.*386G>A
NR_028033.4:n.981G>A
NR_028034.4:n.843G>A
NR_028035.4:n.906G>A
NR_028036.4:n.1044G>A
NR_135313.2:n.961G>A
NR_135314.2:n.1240G>A
NR_135315.2:n.993G>A