Canonical Allele Identifier: CA2610079712

Gene: FAS

Linked Data

• gnomAD v4: 10-89014565-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014565A>C , CM000672.2:g.89014565A>C	GRCh38
NC_000010.10:g.90774322A>C , CM000672.1:g.90774322A>C	GRCh37
NC_000010.9:g.90764302A>C	NCBI36
NG_009089.2:g.29035A>C , LRG_134:g.29035A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1432A>C
ENST00000355740.8:c.*446A>C	ENSP00000347979.3:n.*446A>C
ENST00000357339.7:c.*115A>C	ENSP00000349896.2:n.*115A>C
ENST00000371857.8:n.2668A>C
ENST00000460510.6:c.*115A>C	ENSP00000512812.1:n.*115A>C
ENST00000466081.6:n.2772A>C
ENST00000477270.6:c.*115A>C	ENSP00000512813.1:n.*115A>C
ENST00000479522.6:c.*552A>C	ENSP00000424113.1:n.*552A>C
ENST00000484444.6:c.*564A>C	ENSP00000420975.1:n.*564A>C
ENST00000488877.6:c.1014A>C	ENSP00000425159.1:n.1014A>C
ENST00000492756.7:c.*552A>C	ENSP00000422453.1:n.*552A>C
ENST00000494799.6:c.*115A>C	ENSP00000512834.1:n.*115A>C
ENST00000562983.3:c.*115A>C	ENSP00000512845.1:n.*115A>C
ENST00000612663.6:c.*525A>C	ENSP00000477997.3:n.*525A>C
ENST00000640140.2:n.1268A>C
ENST00000640250.2:n.622A>C
ENST00000640681.2:n.1227A>C
ENST00000696723.1:n.4756A>C
ENST00000696741.1:n.2761A>C
ENST00000696742.1:n.2488A>C
ENST00000696743.1:n.3891A>C
ENST00000696744.1:n.1162A>C
ENST00000696767.1:n.1457A>C
ENST00000696768.1:c.*446A>C	ENSP00000512859.1:n.*446A>C
ENST00000696771.1:c.*115A>C	ENSP00000512860.1:n.*115A>C
ENST00000696772.1:n.2726A>C
ENST00000696773.1:n.2465A>C
ENST00000696774.1:n.6233A>C
ENST00000696776.1:c.*115A>C	ENSP00000512861.1:n.*115A>C
ENST00000696777.1:n.2531A>C
ENST00000696778.1:n.1559A>C
ENST00000696779.1:c.*115A>C	ENSP00000512862.1:n.*115A>C
ENST00000696780.1:c.*115A>C	ENSP00000512863.1:n.*115A>C
ENST00000696781.1:c.*115A>C	ENSP00000512864.1:n.*115A>C
ENST00000696782.1:c.*525A>C	ENSP00000512865.1:n.*525A>C
ENST00000696783.1:n.2991A>C
ENST00000696992.1:n.2240A>C
ENST00000696995.1:n.4652A>C
ENST00000696996.1:n.2565A>C
ENST00000696997.1:c.*753A>C	ENSP00000513028.1:n.*753A>C
ENST00000696998.1:n.2377A>C
ENST00000696999.1:c.*115A>C	ENSP00000513029.1:n.*115A>C
ENST00000697036.1:c.*539A>C	ENSP00000513060.1:n.*539A>C
ENST00000697037.1:n.1158A>C
ENST00000697093.1:n.3359A>C
ENST00000697094.1:n.3706A>C
ENST00000697095.1:c.*2324A>C	ENSP00000513104.1:n.*2324A>C
ENST00000697096.1:n.2256A>C
ENST00000697097.1:c.*115A>C	ENSP00000513105.1:n.*115A>C
ENST00000562983.2:n.1309A>C
ENST00000690268.1:c.*115A>C	ENSP00000509810.1:n.*115A>C
ENST00000355740.7:c.*449A>C	ENSP00000347979.3:n.*449A>C
ENST00000640140.1:n.1295A>C
ENST00000640250.1:n.622A>C
ENST00000640681.1:n.1244A>C
ENST00000652046.1:c.*115A>C MANE Select	ENSP00000498466.1:n.*115A>C
ENST00000352159.8:c.*440A>C	ENSP00000345601.4:n.*440A>C
ENST00000355740.6:c.*115A>C	ENSP00000347979.2:n.*115A>C
ENST00000479522.5:c.*552A>C	ENSP00000424113.1:n.*552A>C
ENST00000484444.5:c.*564A>C	ENSP00000420975.1:n.*564A>C
ENST00000494410.5:c.*481A>C	ENSP00000423755.1:n.*481A>C
NM_000043.4:c.*115A>C , LRG_134t1:c.*115A>C	NP_000034.1:n.*115A>C
NM_152871.2:c.*115A>C	NP_690610.1:n.*115A>C
NM_152872.2:c.*435A>C	NP_690611.1:n.*435A>C
NR_028033.2:n.1297A>C
NR_028034.2:n.1159A>C
NR_028035.2:n.1222A>C
NR_028036.2:n.1360A>C
XM_006717819.2:c.*115A>C	XP_006717882.1:n.*115A>C
XM_011539764.1:c.*115A>C	XP_011538066.1:n.*115A>C
XM_011539765.1:c.*115A>C	XP_011538067.1:n.*115A>C
XM_011539766.1:c.*115A>C	XP_011538068.1:n.*115A>C
XM_011539767.1:c.*115A>C	XP_011538069.1:n.*115A>C
NM_000043.5:c.*115A>C	NP_000034.1:n.*115A>C
NM_001320619.1:c.*446A>C	NP_001307548.1:n.*446A>C
NM_152871.3:c.*115A>C	NP_690610.1:n.*115A>C
NM_152872.3:c.*435A>C	NP_690611.1:n.*435A>C
NR_028033.3:n.1269A>C
NR_028034.3:n.1131A>C
NR_028035.3:n.1194A>C
NR_028036.3:n.1332A>C
NR_135313.1:n.1249A>C
NR_135314.1:n.1432A>C
NR_135315.1:n.1185A>C
XM_006717819.3:c.*115A>C	XP_006717882.1:n.*115A>C
XM_011539764.2:c.*115A>C	XP_011538066.1:n.*115A>C
XM_011539765.2:c.*115A>C	XP_011538067.1:n.*115A>C
XM_011539766.2:c.*115A>C	XP_011538068.1:n.*115A>C
XM_011539767.3:c.*115A>C	XP_011538069.1:n.*115A>C
XR_945732.3:n.1191A>C
XR_945733.2:n.1128A>C
NM_000043.6:c.*115A>C MANE Select	NP_000034.1:n.*115A>C
NM_001320619.2:c.*446A>C	NP_001307548.1:n.*446A>C
NM_152871.4:c.*115A>C	NP_690610.1:n.*115A>C
NM_152872.4:c.*435A>C	NP_690611.1:n.*435A>C
NR_028033.4:n.1030A>C
NR_028034.4:n.892A>C
NR_028035.4:n.955A>C
NR_028036.4:n.1093A>C
NR_135313.2:n.1010A>C
NR_135314.2:n.1289A>C
NR_135315.2:n.1042A>C