Canonical Allele Identifier: CA930982961

Gene: FAS

Linked Data

• dbSNP Id: rs1244008893
• gnomAD v3: 10-89014502-G-T
• gnomAD v4: 10-89014502-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014502G>T , CM000672.2:g.89014502G>T	GRCh38
NC_000010.10:g.90774259G>T , CM000672.1:g.90774259G>T	GRCh37
NC_000010.9:g.90764239G>T	NCBI36
NG_009089.2:g.28972G>T , LRG_134:g.28972G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1369G>T
ENST00000355740.8:c.*383G>T	ENSP00000347979.3:n.*383G>T
ENST00000357339.7:c.*52G>T	ENSP00000349896.2:n.*52G>T
ENST00000371857.8:n.2605G>T
ENST00000460510.6:c.*52G>T	ENSP00000512812.1:n.*52G>T
ENST00000466081.6:n.2709G>T
ENST00000477270.6:c.*52G>T	ENSP00000512813.1:n.*52G>T
ENST00000479522.6:c.*489G>T	ENSP00000424113.1:n.*489G>T
ENST00000484444.6:c.*501G>T	ENSP00000420975.1:n.*501G>T
ENST00000488877.6:c.951G>T	ENSP00000425159.1:n.951G>T
ENST00000492756.7:c.*489G>T	ENSP00000422453.1:n.*489G>T
ENST00000494799.6:c.*52G>T	ENSP00000512834.1:n.*52G>T
ENST00000562983.3:c.*52G>T	ENSP00000512845.1:n.*52G>T
ENST00000612663.6:c.*462G>T	ENSP00000477997.3:n.*462G>T
ENST00000640140.2:n.1205G>T
ENST00000640250.2:n.559G>T
ENST00000640681.2:n.1164G>T
ENST00000696723.1:n.4693G>T
ENST00000696741.1:n.2698G>T
ENST00000696742.1:n.2425G>T
ENST00000696743.1:n.3828G>T
ENST00000696744.1:n.1099G>T
ENST00000696767.1:n.1394G>T
ENST00000696768.1:c.*383G>T	ENSP00000512859.1:n.*383G>T
ENST00000696769.1:n.2749G>T
ENST00000696771.1:c.*52G>T	ENSP00000512860.1:n.*52G>T
ENST00000696772.1:n.2663G>T
ENST00000696773.1:n.2402G>T
ENST00000696774.1:n.6170G>T
ENST00000696776.1:c.*52G>T	ENSP00000512861.1:n.*52G>T
ENST00000696777.1:n.2468G>T
ENST00000696778.1:n.1496G>T
ENST00000696779.1:c.*52G>T	ENSP00000512862.1:n.*52G>T
ENST00000696780.1:c.*52G>T	ENSP00000512863.1:n.*52G>T
ENST00000696781.1:c.*52G>T	ENSP00000512864.1:n.*52G>T
ENST00000696782.1:c.*462G>T	ENSP00000512865.1:n.*462G>T
ENST00000696783.1:n.2928G>T
ENST00000696992.1:n.2177G>T
ENST00000696995.1:n.4589G>T
ENST00000696996.1:n.2502G>T
ENST00000696997.1:c.*690G>T	ENSP00000513028.1:n.*690G>T
ENST00000696998.1:n.2314G>T
ENST00000696999.1:c.*52G>T	ENSP00000513029.1:n.*52G>T
ENST00000697036.1:c.*476G>T	ENSP00000513060.1:n.*476G>T
ENST00000697037.1:n.1095G>T
ENST00000697093.1:n.3296G>T
ENST00000697094.1:n.3643G>T
ENST00000697095.1:c.*2261G>T	ENSP00000513104.1:n.*2261G>T
ENST00000697096.1:n.2193G>T
ENST00000697097.1:c.*52G>T	ENSP00000513105.1:n.*52G>T
ENST00000562983.2:n.1246G>T
ENST00000690268.1:c.*52G>T	ENSP00000509810.1:n.*52G>T
ENST00000355740.7:c.*386G>T	ENSP00000347979.3:n.*386G>T
ENST00000640140.1:n.1232G>T
ENST00000640250.1:n.559G>T
ENST00000640681.1:n.1181G>T
ENST00000652046.1:c.*52G>T MANE Select	ENSP00000498466.1:n.*52G>T
ENST00000352159.8:c.*377G>T	ENSP00000345601.4:n.*377G>T
ENST00000355740.6:c.*52G>T	ENSP00000347979.2:n.*52G>T
ENST00000479522.5:c.*489G>T	ENSP00000424113.1:n.*489G>T
ENST00000484444.5:c.*501G>T	ENSP00000420975.1:n.*501G>T
ENST00000494410.5:c.*418G>T	ENSP00000423755.1:n.*418G>T
NM_000043.4:c.*52G>T , LRG_134t1:c.*52G>T	NP_000034.1:n.*52G>T
NM_152871.2:c.*52G>T	NP_690610.1:n.*52G>T
NM_152872.2:c.*372G>T	NP_690611.1:n.*372G>T
NR_028033.2:n.1234G>T
NR_028034.2:n.1096G>T
NR_028035.2:n.1159G>T
NR_028036.2:n.1297G>T
XM_006717819.2:c.*52G>T	XP_006717882.1:n.*52G>T
XM_011539764.1:c.*52G>T	XP_011538066.1:n.*52G>T
XM_011539765.1:c.*52G>T	XP_011538067.1:n.*52G>T
XM_011539766.1:c.*52G>T	XP_011538068.1:n.*52G>T
XM_011539767.1:c.*52G>T	XP_011538069.1:n.*52G>T
XR_945733.1:n.1065G>T
NM_000043.5:c.*52G>T	NP_000034.1:n.*52G>T
NM_001320619.1:c.*383G>T	NP_001307548.1:n.*383G>T
NM_152871.3:c.*52G>T	NP_690610.1:n.*52G>T
NM_152872.3:c.*372G>T	NP_690611.1:n.*372G>T
NR_028033.3:n.1206G>T
NR_028034.3:n.1068G>T
NR_028035.3:n.1131G>T
NR_028036.3:n.1269G>T
NR_135313.1:n.1186G>T
NR_135314.1:n.1369G>T
NR_135315.1:n.1122G>T
XM_006717819.3:c.*52G>T	XP_006717882.1:n.*52G>T
XM_011539764.2:c.*52G>T	XP_011538066.1:n.*52G>T
XM_011539765.2:c.*52G>T	XP_011538067.1:n.*52G>T
XM_011539766.2:c.*52G>T	XP_011538068.1:n.*52G>T
XM_011539767.3:c.*52G>T	XP_011538069.1:n.*52G>T
XR_945732.3:n.1128G>T
XR_945733.2:n.1065G>T
NM_000043.6:c.*52G>T MANE Select	NP_000034.1:n.*52G>T
NM_001320619.2:c.*383G>T	NP_001307548.1:n.*383G>T
NM_152871.4:c.*52G>T	NP_690610.1:n.*52G>T
NM_152872.4:c.*372G>T	NP_690611.1:n.*372G>T
NR_028033.4:n.967G>T
NR_028034.4:n.829G>T
NR_028035.4:n.892G>T
NR_028036.4:n.1030G>T
NR_135313.2:n.947G>T
NR_135314.2:n.1226G>T
NR_135315.2:n.979G>T