Canonical Allele Identifier: CA2610079714

Gene: FAS

Linked Data

• gnomAD v4: 10-89014567-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014567C>A , CM000672.2:g.89014567C>A	GRCh38
NC_000010.10:g.90774324C>A , CM000672.1:g.90774324C>A	GRCh37
NC_000010.9:g.90764304C>A	NCBI36
NG_009089.2:g.29037C>A , LRG_134:g.29037C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1434C>A
ENST00000355740.8:c.*448C>A	ENSP00000347979.3:n.*448C>A
ENST00000357339.7:c.*117C>A	ENSP00000349896.2:n.*117C>A
ENST00000371857.8:n.2670C>A
ENST00000460510.6:c.*117C>A	ENSP00000512812.1:n.*117C>A
ENST00000466081.6:n.2774C>A
ENST00000477270.6:c.*117C>A	ENSP00000512813.1:n.*117C>A
ENST00000479522.6:c.*554C>A	ENSP00000424113.1:n.*554C>A
ENST00000484444.6:c.*566C>A	ENSP00000420975.1:n.*566C>A
ENST00000488877.6:c.1016C>A	ENSP00000425159.1:n.1016C>A
ENST00000492756.7:c.*554C>A	ENSP00000422453.1:n.*554C>A
ENST00000494799.6:c.*117C>A	ENSP00000512834.1:n.*117C>A
ENST00000562983.3:c.*117C>A	ENSP00000512845.1:n.*117C>A
ENST00000612663.6:c.*527C>A	ENSP00000477997.3:n.*527C>A
ENST00000640140.2:n.1270C>A
ENST00000640250.2:n.624C>A
ENST00000640681.2:n.1229C>A
ENST00000696723.1:n.4758C>A
ENST00000696741.1:n.2763C>A
ENST00000696742.1:n.2490C>A
ENST00000696743.1:n.3893C>A
ENST00000696744.1:n.1164C>A
ENST00000696767.1:n.1459C>A
ENST00000696768.1:c.*448C>A	ENSP00000512859.1:n.*448C>A
ENST00000696771.1:c.*117C>A	ENSP00000512860.1:n.*117C>A
ENST00000696772.1:n.2728C>A
ENST00000696773.1:n.2467C>A
ENST00000696774.1:n.6235C>A
ENST00000696776.1:c.*117C>A	ENSP00000512861.1:n.*117C>A
ENST00000696777.1:n.2533C>A
ENST00000696778.1:n.1561C>A
ENST00000696779.1:c.*117C>A	ENSP00000512862.1:n.*117C>A
ENST00000696780.1:c.*117C>A	ENSP00000512863.1:n.*117C>A
ENST00000696781.1:c.*117C>A	ENSP00000512864.1:n.*117C>A
ENST00000696782.1:c.*527C>A	ENSP00000512865.1:n.*527C>A
ENST00000696783.1:n.2993C>A
ENST00000696992.1:n.2242C>A
ENST00000696995.1:n.4654C>A
ENST00000696996.1:n.2567C>A
ENST00000696997.1:c.*755C>A	ENSP00000513028.1:n.*755C>A
ENST00000696998.1:n.2379C>A
ENST00000696999.1:c.*117C>A	ENSP00000513029.1:n.*117C>A
ENST00000697036.1:c.*541C>A	ENSP00000513060.1:n.*541C>A
ENST00000697037.1:n.1160C>A
ENST00000697093.1:n.3361C>A
ENST00000697094.1:n.3708C>A
ENST00000697095.1:c.*2326C>A	ENSP00000513104.1:n.*2326C>A
ENST00000697096.1:n.2258C>A
ENST00000697097.1:c.*117C>A	ENSP00000513105.1:n.*117C>A
ENST00000562983.2:n.1311C>A
ENST00000690268.1:c.*117C>A	ENSP00000509810.1:n.*117C>A
ENST00000355740.7:c.*451C>A	ENSP00000347979.3:n.*451C>A
ENST00000640140.1:n.1297C>A
ENST00000640250.1:n.624C>A
ENST00000640681.1:n.1246C>A
ENST00000652046.1:c.*117C>A MANE Select	ENSP00000498466.1:n.*117C>A
ENST00000352159.8:c.*442C>A	ENSP00000345601.4:n.*442C>A
ENST00000355740.6:c.*117C>A	ENSP00000347979.2:n.*117C>A
ENST00000479522.5:c.*554C>A	ENSP00000424113.1:n.*554C>A
ENST00000484444.5:c.*566C>A	ENSP00000420975.1:n.*566C>A
ENST00000494410.5:c.*483C>A	ENSP00000423755.1:n.*483C>A
NM_000043.4:c.*117C>A , LRG_134t1:c.*117C>A	NP_000034.1:n.*117C>A
NM_152871.2:c.*117C>A	NP_690610.1:n.*117C>A
NM_152872.2:c.*437C>A	NP_690611.1:n.*437C>A
NR_028033.2:n.1299C>A
NR_028034.2:n.1161C>A
NR_028035.2:n.1224C>A
NR_028036.2:n.1362C>A
XM_006717819.2:c.*117C>A	XP_006717882.1:n.*117C>A
XM_011539764.1:c.*117C>A	XP_011538066.1:n.*117C>A
XM_011539765.1:c.*117C>A	XP_011538067.1:n.*117C>A
XM_011539766.1:c.*117C>A	XP_011538068.1:n.*117C>A
XM_011539767.1:c.*117C>A	XP_011538069.1:n.*117C>A
NM_000043.5:c.*117C>A	NP_000034.1:n.*117C>A
NM_001320619.1:c.*448C>A	NP_001307548.1:n.*448C>A
NM_152871.3:c.*117C>A	NP_690610.1:n.*117C>A
NM_152872.3:c.*437C>A	NP_690611.1:n.*437C>A
NR_028033.3:n.1271C>A
NR_028034.3:n.1133C>A
NR_028035.3:n.1196C>A
NR_028036.3:n.1334C>A
NR_135313.1:n.1251C>A
NR_135314.1:n.1434C>A
NR_135315.1:n.1187C>A
XM_006717819.3:c.*117C>A	XP_006717882.1:n.*117C>A
XM_011539764.2:c.*117C>A	XP_011538066.1:n.*117C>A
XM_011539765.2:c.*117C>A	XP_011538067.1:n.*117C>A
XM_011539766.2:c.*117C>A	XP_011538068.1:n.*117C>A
XM_011539767.3:c.*117C>A	XP_011538069.1:n.*117C>A
XR_945732.3:n.1193C>A
XR_945733.2:n.1130C>A
NM_000043.6:c.*117C>A MANE Select	NP_000034.1:n.*117C>A
NM_001320619.2:c.*448C>A	NP_001307548.1:n.*448C>A
NM_152871.4:c.*117C>A	NP_690610.1:n.*117C>A
NM_152872.4:c.*437C>A	NP_690611.1:n.*437C>A
NR_028033.4:n.1032C>A
NR_028034.4:n.894C>A
NR_028035.4:n.957C>A
NR_028036.4:n.1095C>A
NR_135313.2:n.1012C>A
NR_135314.2:n.1291C>A
NR_135315.2:n.1044C>A