Canonical Allele Identifier: CA2788920983

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014475T>G , CM000672.2:g.89014475T>G	GRCh38
NC_000010.10:g.90774232T>G , CM000672.1:g.90774232T>G	GRCh37
NC_000010.9:g.90764212T>G	NCBI36
NG_009089.2:g.28945T>G , LRG_134:g.28945T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1342T>G
ENST00000355740.8:c.*356T>G	ENSP00000347979.3:n.*356T>G
ENST00000357339.7:c.*25T>G	ENSP00000349896.2:n.*25T>G
ENST00000371857.8:n.2578T>G
ENST00000460510.6:c.*25T>G	ENSP00000512812.1:n.*25T>G
ENST00000466081.6:n.2682T>G
ENST00000477270.6:c.*25T>G	ENSP00000512813.1:n.*25T>G
ENST00000479522.6:c.*462T>G	ENSP00000424113.1:n.*462T>G
ENST00000484444.6:c.*474T>G	ENSP00000420975.1:n.*474T>G
ENST00000488877.6:c.924T>G	ENSP00000425159.1:n.924T>G
ENST00000492756.7:c.*462T>G	ENSP00000422453.1:n.*462T>G
ENST00000494799.6:c.*25T>G	ENSP00000512834.1:n.*25T>G
ENST00000562983.3:c.*25T>G	ENSP00000512845.1:n.*25T>G
ENST00000612663.6:c.*435T>G	ENSP00000477997.3:n.*435T>G
ENST00000640140.2:n.1178T>G
ENST00000640250.2:n.532T>G
ENST00000640681.2:n.1137T>G
ENST00000696723.1:n.4666T>G
ENST00000696741.1:n.2671T>G
ENST00000696742.1:n.2398T>G
ENST00000696743.1:n.3801T>G
ENST00000696744.1:n.1072T>G
ENST00000696767.1:n.1367T>G
ENST00000696768.1:c.*356T>G	ENSP00000512859.1:n.*356T>G
ENST00000696769.1:n.2722T>G
ENST00000696771.1:c.*25T>G	ENSP00000512860.1:n.*25T>G
ENST00000696772.1:n.2636T>G
ENST00000696773.1:n.2375T>G
ENST00000696774.1:n.6143T>G
ENST00000696776.1:c.*25T>G	ENSP00000512861.1:n.*25T>G
ENST00000696777.1:n.2441T>G
ENST00000696778.1:n.1469T>G
ENST00000696779.1:c.*25T>G	ENSP00000512862.1:n.*25T>G
ENST00000696780.1:c.*25T>G	ENSP00000512863.1:n.*25T>G
ENST00000696781.1:c.*25T>G	ENSP00000512864.1:n.*25T>G
ENST00000696782.1:c.*435T>G	ENSP00000512865.1:n.*435T>G
ENST00000696783.1:n.2901T>G
ENST00000696992.1:n.2150T>G
ENST00000696995.1:n.4562T>G
ENST00000696996.1:n.2475T>G
ENST00000696997.1:c.*663T>G	ENSP00000513028.1:n.*663T>G
ENST00000696998.1:n.2287T>G
ENST00000696999.1:c.*25T>G	ENSP00000513029.1:n.*25T>G
ENST00000697036.1:c.*449T>G	ENSP00000513060.1:n.*449T>G
ENST00000697037.1:n.1068T>G
ENST00000697093.1:n.3269T>G
ENST00000697094.1:n.3616T>G
ENST00000697095.1:c.*2234T>G	ENSP00000513104.1:n.*2234T>G
ENST00000697096.1:n.2166T>G
ENST00000697097.1:c.*25T>G	ENSP00000513105.1:n.*25T>G
ENST00000562983.2:n.1219T>G
ENST00000690268.1:c.*25T>G	ENSP00000509810.1:n.*25T>G
ENST00000355740.7:c.*359T>G	ENSP00000347979.3:n.*359T>G
ENST00000640140.1:n.1205T>G
ENST00000640250.1:n.532T>G
ENST00000640681.1:n.1154T>G
ENST00000652046.1:c.*25T>G MANE Select	ENSP00000498466.1:n.*25T>G
ENST00000352159.8:c.*350T>G	ENSP00000345601.4:n.*350T>G
ENST00000355740.6:c.*25T>G	ENSP00000347979.2:n.*25T>G
ENST00000479522.5:c.*462T>G	ENSP00000424113.1:n.*462T>G
ENST00000484444.5:c.*474T>G	ENSP00000420975.1:n.*474T>G
ENST00000494410.5:c.*391T>G	ENSP00000423755.1:n.*391T>G
NM_000043.4:c.*25T>G , LRG_134t1:c.*25T>G	NP_000034.1:n.*25T>G
NM_152871.2:c.*25T>G	NP_690610.1:n.*25T>G
NM_152872.2:c.*345T>G	NP_690611.1:n.*345T>G
NR_028033.2:n.1207T>G
NR_028034.2:n.1069T>G
NR_028035.2:n.1132T>G
NR_028036.2:n.1270T>G
XM_006717819.2:c.*25T>G	XP_006717882.1:n.*25T>G
XM_011539764.1:c.*25T>G	XP_011538066.1:n.*25T>G
XM_011539765.1:c.*25T>G	XP_011538067.1:n.*25T>G
XM_011539766.1:c.*25T>G	XP_011538068.1:n.*25T>G
XM_011539767.1:c.*25T>G	XP_011538069.1:n.*25T>G
XR_945733.1:n.1038T>G
NM_000043.5:c.*25T>G	NP_000034.1:n.*25T>G
NM_001320619.1:c.*356T>G	NP_001307548.1:n.*356T>G
NM_152871.3:c.*25T>G	NP_690610.1:n.*25T>G
NM_152872.3:c.*345T>G	NP_690611.1:n.*345T>G
NR_028033.3:n.1179T>G
NR_028034.3:n.1041T>G
NR_028035.3:n.1104T>G
NR_028036.3:n.1242T>G
NR_135313.1:n.1159T>G
NR_135314.1:n.1342T>G
NR_135315.1:n.1095T>G
XM_006717819.3:c.*25T>G	XP_006717882.1:n.*25T>G
XM_011539764.2:c.*25T>G	XP_011538066.1:n.*25T>G
XM_011539765.2:c.*25T>G	XP_011538067.1:n.*25T>G
XM_011539766.2:c.*25T>G	XP_011538068.1:n.*25T>G
XM_011539767.3:c.*25T>G	XP_011538069.1:n.*25T>G
XR_945732.3:n.1101T>G
XR_945733.2:n.1038T>G
NM_000043.6:c.*25T>G MANE Select	NP_000034.1:n.*25T>G
NM_001320619.2:c.*356T>G	NP_001307548.1:n.*356T>G
NM_152871.4:c.*25T>G	NP_690610.1:n.*25T>G
NM_152872.4:c.*345T>G	NP_690611.1:n.*345T>G
NR_028033.4:n.940T>G
NR_028034.4:n.802T>G
NR_028035.4:n.865T>G
NR_028036.4:n.1003T>G
NR_135313.2:n.920T>G
NR_135314.2:n.1199T>G
NR_135315.2:n.952T>G