Canonical Allele Identifier: CA594943275

Gene: FAS

Linked Data

• dbSNP Id: rs1246869490
• gnomAD v2: 10-90774400-G-A
• gnomAD v3: 10-89014643-G-A
• gnomAD v4: 10-89014643-G-A
• MyVariant Identifiers: chr10:g.90774400G>A (hg19) ; chr10:g.89014643G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014643G>A , CM000672.2:g.89014643G>A	GRCh38
NC_000010.10:g.90774400G>A , CM000672.1:g.90774400G>A	GRCh37
NC_000010.9:g.90764380G>A	NCBI36
NG_009089.2:g.29113G>A , LRG_134:g.29113G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1510G>A
ENST00000355740.8:c.*524G>A	ENSP00000347979.3:n.*524G>A
ENST00000357339.7:c.*193G>A	ENSP00000349896.2:n.*193G>A
ENST00000371857.8:n.2746G>A
ENST00000460510.6:c.*193G>A	ENSP00000512812.1:n.*193G>A
ENST00000466081.6:n.2850G>A
ENST00000477270.6:c.*193G>A	ENSP00000512813.1:n.*193G>A
ENST00000488877.6:c.1092G>A	ENSP00000425159.1:n.1092G>A
ENST00000492756.7:c.*630G>A	ENSP00000422453.1:n.*630G>A
ENST00000494799.6:c.*193G>A	ENSP00000512834.1:n.*193G>A
ENST00000562983.3:c.*193G>A	ENSP00000512845.1:n.*193G>A
ENST00000612663.6:c.*603G>A	ENSP00000477997.3:n.*603G>A
ENST00000640140.2:n.1346G>A
ENST00000640250.2:n.700G>A
ENST00000640681.2:n.1305G>A
ENST00000696723.1:n.4834G>A
ENST00000696741.1:n.2839G>A
ENST00000696742.1:n.2566G>A
ENST00000696743.1:n.3969G>A
ENST00000696744.1:n.1240G>A
ENST00000696767.1:n.1535G>A
ENST00000696768.1:c.*524G>A	ENSP00000512859.1:n.*524G>A
ENST00000696771.1:c.*193G>A	ENSP00000512860.1:n.*193G>A
ENST00000696772.1:n.2804G>A
ENST00000696773.1:n.2543G>A
ENST00000696774.1:n.6311G>A
ENST00000696776.1:c.*193G>A	ENSP00000512861.1:n.*193G>A
ENST00000696777.1:n.2609G>A
ENST00000696778.1:n.1637G>A
ENST00000696779.1:c.*193G>A	ENSP00000512862.1:n.*193G>A
ENST00000696780.1:c.*193G>A	ENSP00000512863.1:n.*193G>A
ENST00000696781.1:c.*193G>A	ENSP00000512864.1:n.*193G>A
ENST00000696782.1:c.*603G>A	ENSP00000512865.1:n.*603G>A
ENST00000696783.1:n.3069G>A
ENST00000696992.1:n.2318G>A
ENST00000696995.1:n.4730G>A
ENST00000696996.1:n.2643G>A
ENST00000696997.1:c.*831G>A	ENSP00000513028.1:n.*831G>A
ENST00000696998.1:n.2455G>A
ENST00000696999.1:c.*193G>A	ENSP00000513029.1:n.*193G>A
ENST00000697036.1:c.*617G>A	ENSP00000513060.1:n.*617G>A
ENST00000697037.1:n.1236G>A
ENST00000697093.1:n.3437G>A
ENST00000697094.1:n.3784G>A
ENST00000697095.1:c.*2402G>A	ENSP00000513104.1:n.*2402G>A
ENST00000697096.1:n.2334G>A
ENST00000697097.1:c.*193G>A	ENSP00000513105.1:n.*193G>A
ENST00000562983.2:n.1387G>A
ENST00000690268.1:c.*193G>A	ENSP00000509810.1:n.*193G>A
ENST00000355740.7:c.*527G>A	ENSP00000347979.3:n.*527G>A
ENST00000640140.1:n.1373G>A
ENST00000640250.1:n.700G>A
ENST00000640681.1:n.1322G>A
ENST00000652046.1:c.*193G>A MANE Select	ENSP00000498466.1:n.*193G>A
ENST00000352159.8:c.*518G>A	ENSP00000345601.4:n.*518G>A
ENST00000355740.6:c.*193G>A	ENSP00000347979.2:n.*193G>A
NM_000043.4:c.*193G>A , LRG_134t1:c.*193G>A	NP_000034.1:n.*193G>A
NM_152871.2:c.*193G>A	NP_690610.1:n.*193G>A
NM_152872.2:c.*513G>A	NP_690611.1:n.*513G>A
NR_028033.2:n.1375G>A
NR_028034.2:n.1237G>A
NR_028035.2:n.1300G>A
NR_028036.2:n.1438G>A
XM_006717819.2:c.*193G>A	XP_006717882.1:n.*193G>A
XM_011539764.1:c.*193G>A	XP_011538066.1:n.*193G>A
XM_011539765.1:c.*193G>A	XP_011538067.1:n.*193G>A
XM_011539766.1:c.*193G>A	XP_011538068.1:n.*193G>A
XM_011539767.1:c.*193G>A	XP_011538069.1:n.*193G>A
NM_000043.5:c.*193G>A	NP_000034.1:n.*193G>A
NM_001320619.1:c.*524G>A	NP_001307548.1:n.*524G>A
NM_152871.3:c.*193G>A	NP_690610.1:n.*193G>A
NM_152872.3:c.*513G>A	NP_690611.1:n.*513G>A
NR_028033.3:n.1347G>A
NR_028034.3:n.1209G>A
NR_028035.3:n.1272G>A
NR_028036.3:n.1410G>A
NR_135313.1:n.1327G>A
NR_135314.1:n.1510G>A
NR_135315.1:n.1263G>A
XM_006717819.3:c.*193G>A	XP_006717882.1:n.*193G>A
XM_011539764.2:c.*193G>A	XP_011538066.1:n.*193G>A
XM_011539765.2:c.*193G>A	XP_011538067.1:n.*193G>A
XM_011539766.2:c.*193G>A	XP_011538068.1:n.*193G>A
XM_011539767.3:c.*193G>A	XP_011538069.1:n.*193G>A
XR_945732.3:n.1269G>A
XR_945733.2:n.1206G>A
NM_000043.6:c.*193G>A MANE Select	NP_000034.1:n.*193G>A
NM_001320619.2:c.*524G>A	NP_001307548.1:n.*524G>A
NM_152871.4:c.*193G>A	NP_690610.1:n.*193G>A
NM_152872.4:c.*513G>A	NP_690611.1:n.*513G>A
NR_028033.4:n.1108G>A
NR_028034.4:n.970G>A
NR_028035.4:n.1033G>A
NR_028036.4:n.1171G>A
NR_135313.2:n.1088G>A
NR_135314.2:n.1367G>A
NR_135315.2:n.1120G>A