Canonical Allele Identifier: CA2610079701

Gene: FAS

Linked Data

• gnomAD v4: 10-89014556-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014557dup , CM000672.2:g.89014557dup	GRCh38
NC_000010.10:g.90774314dup , CM000672.1:g.90774314dup	GRCh37
NC_000010.9:g.90764294dup	NCBI36
NG_009089.2:g.29027dup , LRG_134:g.29027dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1424dup
ENST00000355740.8:c.*438dup	ENSP00000347979.3:n.*438dup
ENST00000357339.7:c.*107dup	ENSP00000349896.2:n.*107dup
ENST00000371857.8:n.2660dup
ENST00000460510.6:c.*107dup	ENSP00000512812.1:n.*107dup
ENST00000466081.6:n.2764dup
ENST00000477270.6:c.*107dup	ENSP00000512813.1:n.*107dup
ENST00000479522.6:c.*544dup	ENSP00000424113.1:n.*544dup
ENST00000484444.6:c.*556dup	ENSP00000420975.1:n.*556dup
ENST00000488877.6:c.1006dup	ENSP00000425159.1:n.1006dup
ENST00000492756.7:c.*544dup	ENSP00000422453.1:n.*544dup
ENST00000494799.6:c.*107dup	ENSP00000512834.1:n.*107dup
ENST00000562983.3:c.*107dup	ENSP00000512845.1:n.*107dup
ENST00000612663.6:c.*517dup	ENSP00000477997.3:n.*517dup
ENST00000640140.2:n.1260dup
ENST00000640250.2:n.614dup
ENST00000640681.2:n.1219dup
ENST00000696723.1:n.4748dup
ENST00000696741.1:n.2753dup
ENST00000696742.1:n.2480dup
ENST00000696743.1:n.3883dup
ENST00000696744.1:n.1154dup
ENST00000696767.1:n.1449dup
ENST00000696768.1:c.*438dup	ENSP00000512859.1:n.*438dup
ENST00000696769.1:n.2804dup
ENST00000696771.1:c.*107dup	ENSP00000512860.1:n.*107dup
ENST00000696772.1:n.2718dup
ENST00000696773.1:n.2457dup
ENST00000696774.1:n.6225dup
ENST00000696776.1:c.*107dup	ENSP00000512861.1:n.*107dup
ENST00000696777.1:n.2523dup
ENST00000696778.1:n.1551dup
ENST00000696779.1:c.*107dup	ENSP00000512862.1:n.*107dup
ENST00000696780.1:c.*107dup	ENSP00000512863.1:n.*107dup
ENST00000696781.1:c.*107dup	ENSP00000512864.1:n.*107dup
ENST00000696782.1:c.*517dup	ENSP00000512865.1:n.*517dup
ENST00000696783.1:n.2983dup
ENST00000696992.1:n.2232dup
ENST00000696995.1:n.4644dup
ENST00000696996.1:n.2557dup
ENST00000696997.1:c.*745dup	ENSP00000513028.1:n.*745dup
ENST00000696998.1:n.2369dup
ENST00000696999.1:c.*107dup	ENSP00000513029.1:n.*107dup
ENST00000697036.1:c.*531dup	ENSP00000513060.1:n.*531dup
ENST00000697037.1:n.1150dup
ENST00000697093.1:n.3351dup
ENST00000697094.1:n.3698dup
ENST00000697095.1:c.*2316dup	ENSP00000513104.1:n.*2316dup
ENST00000697096.1:n.2248dup
ENST00000697097.1:c.*107dup	ENSP00000513105.1:n.*107dup
ENST00000562983.2:n.1301dup
ENST00000690268.1:c.*107dup	ENSP00000509810.1:n.*107dup
ENST00000355740.7:c.*441dup	ENSP00000347979.3:n.*441dup
ENST00000640140.1:n.1287dup
ENST00000640250.1:n.614dup
ENST00000640681.1:n.1236dup
ENST00000652046.1:c.*107dup MANE Select	ENSP00000498466.1:n.*107dup
ENST00000352159.8:c.*432dup	ENSP00000345601.4:n.*432dup
ENST00000355740.6:c.*107dup	ENSP00000347979.2:n.*107dup
ENST00000479522.5:c.*544dup	ENSP00000424113.1:n.*544dup
ENST00000484444.5:c.*556dup	ENSP00000420975.1:n.*556dup
ENST00000494410.5:c.*473dup	ENSP00000423755.1:n.*473dup
NM_000043.4:c.*107dup , LRG_134t1:c.*107dup	NP_000034.1:n.*107dup
NM_152871.2:c.*107dup	NP_690610.1:n.*107dup
NM_152872.2:c.*427dup	NP_690611.1:n.*427dup
NR_028033.2:n.1289dup
NR_028034.2:n.1151dup
NR_028035.2:n.1214dup
NR_028036.2:n.1352dup
XM_006717819.2:c.*107dup	XP_006717882.1:n.*107dup
XM_011539764.1:c.*107dup	XP_011538066.1:n.*107dup
XM_011539765.1:c.*107dup	XP_011538067.1:n.*107dup
XM_011539766.1:c.*107dup	XP_011538068.1:n.*107dup
XM_011539767.1:c.*107dup	XP_011538069.1:n.*107dup
NM_000043.5:c.*107dup	NP_000034.1:n.*107dup
NM_001320619.1:c.*438dup	NP_001307548.1:n.*438dup
NM_152871.3:c.*107dup	NP_690610.1:n.*107dup
NM_152872.3:c.*427dup	NP_690611.1:n.*427dup
NR_028033.3:n.1261dup
NR_028034.3:n.1123dup
NR_028035.3:n.1186dup
NR_028036.3:n.1324dup
NR_135313.1:n.1241dup
NR_135314.1:n.1424dup
NR_135315.1:n.1177dup
XM_006717819.3:c.*107dup	XP_006717882.1:n.*107dup
XM_011539764.2:c.*107dup	XP_011538066.1:n.*107dup
XM_011539765.2:c.*107dup	XP_011538067.1:n.*107dup
XM_011539766.2:c.*107dup	XP_011538068.1:n.*107dup
XM_011539767.3:c.*107dup	XP_011538069.1:n.*107dup
XR_945732.3:n.1183dup
XR_945733.2:n.1120dup
NM_000043.6:c.*107dup MANE Select	NP_000034.1:n.*107dup
NM_001320619.2:c.*438dup	NP_001307548.1:n.*438dup
NM_152871.4:c.*107dup	NP_690610.1:n.*107dup
NM_152872.4:c.*427dup	NP_690611.1:n.*427dup
NR_028033.4:n.1022dup
NR_028034.4:n.884dup
NR_028035.4:n.947dup
NR_028036.4:n.1085dup
NR_135313.2:n.1002dup
NR_135314.2:n.1281dup
NR_135315.2:n.1034dup