Canonical Allele Identifier: CA211335388

Gene: FAS

Linked Data

• dbSNP Id: rs367859151
• gnomAD v4: 10-89014478-G-T
• MyVariant Identifiers: chr10:g.90774235G>T (hg19) ; chr10:g.89014478G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014478G>T , CM000672.2:g.89014478G>T	GRCh38
NC_000010.10:g.90774235G>T , CM000672.1:g.90774235G>T	GRCh37
NC_000010.9:g.90764215G>T	NCBI36
NG_009089.2:g.28948G>T , LRG_134:g.28948G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1345G>T
ENST00000355740.8:c.*359G>T	ENSP00000347979.3:n.*359G>T
ENST00000357339.7:c.*28G>T	ENSP00000349896.2:n.*28G>T
ENST00000371857.8:n.2581G>T
ENST00000460510.6:c.*28G>T	ENSP00000512812.1:n.*28G>T
ENST00000466081.6:n.2685G>T
ENST00000477270.6:c.*28G>T	ENSP00000512813.1:n.*28G>T
ENST00000479522.6:c.*465G>T	ENSP00000424113.1:n.*465G>T
ENST00000484444.6:c.*477G>T	ENSP00000420975.1:n.*477G>T
ENST00000488877.6:c.927G>T	ENSP00000425159.1:n.927G>T
ENST00000492756.7:c.*465G>T	ENSP00000422453.1:n.*465G>T
ENST00000494799.6:c.*28G>T	ENSP00000512834.1:n.*28G>T
ENST00000562983.3:c.*28G>T	ENSP00000512845.1:n.*28G>T
ENST00000612663.6:c.*438G>T	ENSP00000477997.3:n.*438G>T
ENST00000640140.2:n.1181G>T
ENST00000640250.2:n.535G>T
ENST00000640681.2:n.1140G>T
ENST00000696723.1:n.4669G>T
ENST00000696741.1:n.2674G>T
ENST00000696742.1:n.2401G>T
ENST00000696743.1:n.3804G>T
ENST00000696744.1:n.1075G>T
ENST00000696767.1:n.1370G>T
ENST00000696768.1:c.*359G>T	ENSP00000512859.1:n.*359G>T
ENST00000696769.1:n.2725G>T
ENST00000696771.1:c.*28G>T	ENSP00000512860.1:n.*28G>T
ENST00000696772.1:n.2639G>T
ENST00000696773.1:n.2378G>T
ENST00000696774.1:n.6146G>T
ENST00000696776.1:c.*28G>T	ENSP00000512861.1:n.*28G>T
ENST00000696777.1:n.2444G>T
ENST00000696778.1:n.1472G>T
ENST00000696779.1:c.*28G>T	ENSP00000512862.1:n.*28G>T
ENST00000696780.1:c.*28G>T	ENSP00000512863.1:n.*28G>T
ENST00000696781.1:c.*28G>T	ENSP00000512864.1:n.*28G>T
ENST00000696782.1:c.*438G>T	ENSP00000512865.1:n.*438G>T
ENST00000696783.1:n.2904G>T
ENST00000696992.1:n.2153G>T
ENST00000696995.1:n.4565G>T
ENST00000696996.1:n.2478G>T
ENST00000696997.1:c.*666G>T	ENSP00000513028.1:n.*666G>T
ENST00000696998.1:n.2290G>T
ENST00000696999.1:c.*28G>T	ENSP00000513029.1:n.*28G>T
ENST00000697036.1:c.*452G>T	ENSP00000513060.1:n.*452G>T
ENST00000697037.1:n.1071G>T
ENST00000697093.1:n.3272G>T
ENST00000697094.1:n.3619G>T
ENST00000697095.1:c.*2237G>T	ENSP00000513104.1:n.*2237G>T
ENST00000697096.1:n.2169G>T
ENST00000697097.1:c.*28G>T	ENSP00000513105.1:n.*28G>T
ENST00000562983.2:n.1222G>T
ENST00000690268.1:c.*28G>T	ENSP00000509810.1:n.*28G>T
ENST00000355740.7:c.*362G>T	ENSP00000347979.3:n.*362G>T
ENST00000640140.1:n.1208G>T
ENST00000640250.1:n.535G>T
ENST00000640681.1:n.1157G>T
ENST00000652046.1:c.*28G>T MANE Select	ENSP00000498466.1:n.*28G>T
ENST00000352159.8:c.*353G>T	ENSP00000345601.4:n.*353G>T
ENST00000355740.6:c.*28G>T	ENSP00000347979.2:n.*28G>T
ENST00000479522.5:c.*465G>T	ENSP00000424113.1:n.*465G>T
ENST00000484444.5:c.*477G>T	ENSP00000420975.1:n.*477G>T
ENST00000494410.5:c.*394G>T	ENSP00000423755.1:n.*394G>T
NM_000043.4:c.*28G>T , LRG_134t1:c.*28G>T	NP_000034.1:n.*28G>T
NM_152871.2:c.*28G>T	NP_690610.1:n.*28G>T
NM_152872.2:c.*348G>T	NP_690611.1:n.*348G>T
NR_028033.2:n.1210G>T
NR_028034.2:n.1072G>T
NR_028035.2:n.1135G>T
NR_028036.2:n.1273G>T
XM_006717819.2:c.*28G>T	XP_006717882.1:n.*28G>T
XM_011539764.1:c.*28G>T	XP_011538066.1:n.*28G>T
XM_011539765.1:c.*28G>T	XP_011538067.1:n.*28G>T
XM_011539766.1:c.*28G>T	XP_011538068.1:n.*28G>T
XM_011539767.1:c.*28G>T	XP_011538069.1:n.*28G>T
XR_945733.1:n.1041G>T
NM_000043.5:c.*28G>T	NP_000034.1:n.*28G>T
NM_001320619.1:c.*359G>T	NP_001307548.1:n.*359G>T
NM_152871.3:c.*28G>T	NP_690610.1:n.*28G>T
NM_152872.3:c.*348G>T	NP_690611.1:n.*348G>T
NR_028033.3:n.1182G>T
NR_028034.3:n.1044G>T
NR_028035.3:n.1107G>T
NR_028036.3:n.1245G>T
NR_135313.1:n.1162G>T
NR_135314.1:n.1345G>T
NR_135315.1:n.1098G>T
XM_006717819.3:c.*28G>T	XP_006717882.1:n.*28G>T
XM_011539764.2:c.*28G>T	XP_011538066.1:n.*28G>T
XM_011539765.2:c.*28G>T	XP_011538067.1:n.*28G>T
XM_011539766.2:c.*28G>T	XP_011538068.1:n.*28G>T
XM_011539767.3:c.*28G>T	XP_011538069.1:n.*28G>T
XR_945732.3:n.1104G>T
XR_945733.2:n.1041G>T
NM_000043.6:c.*28G>T MANE Select	NP_000034.1:n.*28G>T
NM_001320619.2:c.*359G>T	NP_001307548.1:n.*359G>T
NM_152871.4:c.*28G>T	NP_690610.1:n.*28G>T
NM_152872.4:c.*348G>T	NP_690611.1:n.*348G>T
NR_028033.4:n.943G>T
NR_028034.4:n.805G>T
NR_028035.4:n.868G>T
NR_028036.4:n.1006G>T
NR_135313.2:n.923G>T
NR_135314.2:n.1202G>T
NR_135315.2:n.955G>T