Canonical Allele Identifier: CA594943260

Gene: FAS

Linked Data

• dbSNP Id: rs969476730
• gnomAD v2: 10-90774345-G-T
• gnomAD v4: 10-89014588-G-T
• MyVariant Identifiers: chr10:g.90774345G>T (hg19) ; chr10:g.89014588G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014588G>T , CM000672.2:g.89014588G>T	GRCh38
NC_000010.10:g.90774345G>T , CM000672.1:g.90774345G>T	GRCh37
NC_000010.9:g.90764325G>T	NCBI36
NG_009089.2:g.29058G>T , LRG_134:g.29058G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1455G>T
ENST00000355740.8:c.*469G>T	ENSP00000347979.3:n.*469G>T
ENST00000357339.7:c.*138G>T	ENSP00000349896.2:n.*138G>T
ENST00000371857.8:n.2691G>T
ENST00000460510.6:c.*138G>T	ENSP00000512812.1:n.*138G>T
ENST00000466081.6:n.2795G>T
ENST00000477270.6:c.*138G>T	ENSP00000512813.1:n.*138G>T
ENST00000488877.6:c.1037G>T	ENSP00000425159.1:n.1037G>T
ENST00000492756.7:c.*575G>T	ENSP00000422453.1:n.*575G>T
ENST00000494799.6:c.*138G>T	ENSP00000512834.1:n.*138G>T
ENST00000562983.3:c.*138G>T	ENSP00000512845.1:n.*138G>T
ENST00000612663.6:c.*548G>T	ENSP00000477997.3:n.*548G>T
ENST00000640140.2:n.1291G>T
ENST00000640250.2:n.645G>T
ENST00000640681.2:n.1250G>T
ENST00000696723.1:n.4779G>T
ENST00000696741.1:n.2784G>T
ENST00000696742.1:n.2511G>T
ENST00000696743.1:n.3914G>T
ENST00000696744.1:n.1185G>T
ENST00000696767.1:n.1480G>T
ENST00000696768.1:c.*469G>T	ENSP00000512859.1:n.*469G>T
ENST00000696771.1:c.*138G>T	ENSP00000512860.1:n.*138G>T
ENST00000696772.1:n.2749G>T
ENST00000696773.1:n.2488G>T
ENST00000696774.1:n.6256G>T
ENST00000696776.1:c.*138G>T	ENSP00000512861.1:n.*138G>T
ENST00000696777.1:n.2554G>T
ENST00000696778.1:n.1582G>T
ENST00000696779.1:c.*138G>T	ENSP00000512862.1:n.*138G>T
ENST00000696780.1:c.*138G>T	ENSP00000512863.1:n.*138G>T
ENST00000696781.1:c.*138G>T	ENSP00000512864.1:n.*138G>T
ENST00000696782.1:c.*548G>T	ENSP00000512865.1:n.*548G>T
ENST00000696783.1:n.3014G>T
ENST00000696992.1:n.2263G>T
ENST00000696995.1:n.4675G>T
ENST00000696996.1:n.2588G>T
ENST00000696997.1:c.*776G>T	ENSP00000513028.1:n.*776G>T
ENST00000696998.1:n.2400G>T
ENST00000696999.1:c.*138G>T	ENSP00000513029.1:n.*138G>T
ENST00000697036.1:c.*562G>T	ENSP00000513060.1:n.*562G>T
ENST00000697037.1:n.1181G>T
ENST00000697093.1:n.3382G>T
ENST00000697094.1:n.3729G>T
ENST00000697095.1:c.*2347G>T	ENSP00000513104.1:n.*2347G>T
ENST00000697096.1:n.2279G>T
ENST00000697097.1:c.*138G>T	ENSP00000513105.1:n.*138G>T
ENST00000562983.2:n.1332G>T
ENST00000690268.1:c.*138G>T	ENSP00000509810.1:n.*138G>T
ENST00000355740.7:c.*472G>T	ENSP00000347979.3:n.*472G>T
ENST00000640140.1:n.1318G>T
ENST00000640250.1:n.645G>T
ENST00000640681.1:n.1267G>T
ENST00000652046.1:c.*138G>T MANE Select	ENSP00000498466.1:n.*138G>T
ENST00000352159.8:c.*463G>T	ENSP00000345601.4:n.*463G>T
ENST00000355740.6:c.*138G>T	ENSP00000347979.2:n.*138G>T
ENST00000484444.5:c.*587G>T	ENSP00000420975.1:n.*587G>T
NM_000043.4:c.*138G>T , LRG_134t1:c.*138G>T	NP_000034.1:n.*138G>T
NM_152871.2:c.*138G>T	NP_690610.1:n.*138G>T
NM_152872.2:c.*458G>T	NP_690611.1:n.*458G>T
NR_028033.2:n.1320G>T
NR_028034.2:n.1182G>T
NR_028035.2:n.1245G>T
NR_028036.2:n.1383G>T
XM_006717819.2:c.*138G>T	XP_006717882.1:n.*138G>T
XM_011539764.1:c.*138G>T	XP_011538066.1:n.*138G>T
XM_011539765.1:c.*138G>T	XP_011538067.1:n.*138G>T
XM_011539766.1:c.*138G>T	XP_011538068.1:n.*138G>T
XM_011539767.1:c.*138G>T	XP_011538069.1:n.*138G>T
NM_000043.5:c.*138G>T	NP_000034.1:n.*138G>T
NM_001320619.1:c.*469G>T	NP_001307548.1:n.*469G>T
NM_152871.3:c.*138G>T	NP_690610.1:n.*138G>T
NM_152872.3:c.*458G>T	NP_690611.1:n.*458G>T
NR_028033.3:n.1292G>T
NR_028034.3:n.1154G>T
NR_028035.3:n.1217G>T
NR_028036.3:n.1355G>T
NR_135313.1:n.1272G>T
NR_135314.1:n.1455G>T
NR_135315.1:n.1208G>T
XM_006717819.3:c.*138G>T	XP_006717882.1:n.*138G>T
XM_011539764.2:c.*138G>T	XP_011538066.1:n.*138G>T
XM_011539765.2:c.*138G>T	XP_011538067.1:n.*138G>T
XM_011539766.2:c.*138G>T	XP_011538068.1:n.*138G>T
XM_011539767.3:c.*138G>T	XP_011538069.1:n.*138G>T
XR_945732.3:n.1214G>T
XR_945733.2:n.1151G>T
NM_000043.6:c.*138G>T MANE Select	NP_000034.1:n.*138G>T
NM_001320619.2:c.*469G>T	NP_001307548.1:n.*469G>T
NM_152871.4:c.*138G>T	NP_690610.1:n.*138G>T
NM_152872.4:c.*458G>T	NP_690611.1:n.*458G>T
NR_028033.4:n.1053G>T
NR_028034.4:n.915G>T
NR_028035.4:n.978G>T
NR_028036.4:n.1116G>T
NR_135313.2:n.1033G>T
NR_135314.2:n.1312G>T
NR_135315.2:n.1065G>T