Canonical Allele Identifier: CA595185135

Gene: FAS

Linked Data

• dbSNP Id: rs1299534672
• gnomAD v2: 10-90774274-G-A
• gnomAD v4: 10-89014517-G-A
• MyVariant Identifiers: chr10:g.90774274G>A (hg19) ; chr10:g.89014517G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014517G>A , CM000672.2:g.89014517G>A	GRCh38
NC_000010.10:g.90774274G>A , CM000672.1:g.90774274G>A	GRCh37
NC_000010.9:g.90764254G>A	NCBI36
NG_009089.2:g.28987G>A , LRG_134:g.28987G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1384G>A
ENST00000355740.8:c.*398G>A	ENSP00000347979.3:n.*398G>A
ENST00000357339.7:c.*67G>A	ENSP00000349896.2:n.*67G>A
ENST00000371857.8:n.2620G>A
ENST00000460510.6:c.*67G>A	ENSP00000512812.1:n.*67G>A
ENST00000466081.6:n.2724G>A
ENST00000477270.6:c.*67G>A	ENSP00000512813.1:n.*67G>A
ENST00000479522.6:c.*504G>A	ENSP00000424113.1:n.*504G>A
ENST00000484444.6:c.*516G>A	ENSP00000420975.1:n.*516G>A
ENST00000488877.6:c.966G>A	ENSP00000425159.1:n.966G>A
ENST00000492756.7:c.*504G>A	ENSP00000422453.1:n.*504G>A
ENST00000494799.6:c.*67G>A	ENSP00000512834.1:n.*67G>A
ENST00000562983.3:c.*67G>A	ENSP00000512845.1:n.*67G>A
ENST00000612663.6:c.*477G>A	ENSP00000477997.3:n.*477G>A
ENST00000640140.2:n.1220G>A
ENST00000640250.2:n.574G>A
ENST00000640681.2:n.1179G>A
ENST00000696723.1:n.4708G>A
ENST00000696741.1:n.2713G>A
ENST00000696742.1:n.2440G>A
ENST00000696743.1:n.3843G>A
ENST00000696744.1:n.1114G>A
ENST00000696767.1:n.1409G>A
ENST00000696768.1:c.*398G>A	ENSP00000512859.1:n.*398G>A
ENST00000696769.1:n.2764G>A
ENST00000696771.1:c.*67G>A	ENSP00000512860.1:n.*67G>A
ENST00000696772.1:n.2678G>A
ENST00000696773.1:n.2417G>A
ENST00000696774.1:n.6185G>A
ENST00000696776.1:c.*67G>A	ENSP00000512861.1:n.*67G>A
ENST00000696777.1:n.2483G>A
ENST00000696778.1:n.1511G>A
ENST00000696779.1:c.*67G>A	ENSP00000512862.1:n.*67G>A
ENST00000696780.1:c.*67G>A	ENSP00000512863.1:n.*67G>A
ENST00000696781.1:c.*67G>A	ENSP00000512864.1:n.*67G>A
ENST00000696782.1:c.*477G>A	ENSP00000512865.1:n.*477G>A
ENST00000696783.1:n.2943G>A
ENST00000696992.1:n.2192G>A
ENST00000696995.1:n.4604G>A
ENST00000696996.1:n.2517G>A
ENST00000696997.1:c.*705G>A	ENSP00000513028.1:n.*705G>A
ENST00000696998.1:n.2329G>A
ENST00000696999.1:c.*67G>A	ENSP00000513029.1:n.*67G>A
ENST00000697036.1:c.*491G>A	ENSP00000513060.1:n.*491G>A
ENST00000697037.1:n.1110G>A
ENST00000697093.1:n.3311G>A
ENST00000697094.1:n.3658G>A
ENST00000697095.1:c.*2276G>A	ENSP00000513104.1:n.*2276G>A
ENST00000697096.1:n.2208G>A
ENST00000697097.1:c.*67G>A	ENSP00000513105.1:n.*67G>A
ENST00000562983.2:n.1261G>A
ENST00000690268.1:c.*67G>A	ENSP00000509810.1:n.*67G>A
ENST00000355740.7:c.*401G>A	ENSP00000347979.3:n.*401G>A
ENST00000640140.1:n.1247G>A
ENST00000640250.1:n.574G>A
ENST00000640681.1:n.1196G>A
ENST00000652046.1:c.*67G>A MANE Select	ENSP00000498466.1:n.*67G>A
ENST00000352159.8:c.*392G>A	ENSP00000345601.4:n.*392G>A
ENST00000355740.6:c.*67G>A	ENSP00000347979.2:n.*67G>A
ENST00000479522.5:c.*504G>A	ENSP00000424113.1:n.*504G>A
ENST00000484444.5:c.*516G>A	ENSP00000420975.1:n.*516G>A
ENST00000494410.5:c.*433G>A	ENSP00000423755.1:n.*433G>A
NM_000043.4:c.*67G>A , LRG_134t1:c.*67G>A	NP_000034.1:n.*67G>A
NM_152871.2:c.*67G>A	NP_690610.1:n.*67G>A
NM_152872.2:c.*387G>A	NP_690611.1:n.*387G>A
NR_028033.2:n.1249G>A
NR_028034.2:n.1111G>A
NR_028035.2:n.1174G>A
NR_028036.2:n.1312G>A
XM_006717819.2:c.*67G>A	XP_006717882.1:n.*67G>A
XM_011539764.1:c.*67G>A	XP_011538066.1:n.*67G>A
XM_011539765.1:c.*67G>A	XP_011538067.1:n.*67G>A
XM_011539766.1:c.*67G>A	XP_011538068.1:n.*67G>A
XM_011539767.1:c.*67G>A	XP_011538069.1:n.*67G>A
NM_000043.5:c.*67G>A	NP_000034.1:n.*67G>A
NM_001320619.1:c.*398G>A	NP_001307548.1:n.*398G>A
NM_152871.3:c.*67G>A	NP_690610.1:n.*67G>A
NM_152872.3:c.*387G>A	NP_690611.1:n.*387G>A
NR_028033.3:n.1221G>A
NR_028034.3:n.1083G>A
NR_028035.3:n.1146G>A
NR_028036.3:n.1284G>A
NR_135313.1:n.1201G>A
NR_135314.1:n.1384G>A
NR_135315.1:n.1137G>A
XM_006717819.3:c.*67G>A	XP_006717882.1:n.*67G>A
XM_011539764.2:c.*67G>A	XP_011538066.1:n.*67G>A
XM_011539765.2:c.*67G>A	XP_011538067.1:n.*67G>A
XM_011539766.2:c.*67G>A	XP_011538068.1:n.*67G>A
XM_011539767.3:c.*67G>A	XP_011538069.1:n.*67G>A
XR_945732.3:n.1143G>A
XR_945733.2:n.1080G>A
NM_000043.6:c.*67G>A MANE Select	NP_000034.1:n.*67G>A
NM_001320619.2:c.*398G>A	NP_001307548.1:n.*398G>A
NM_152871.4:c.*67G>A	NP_690610.1:n.*67G>A
NM_152872.4:c.*387G>A	NP_690611.1:n.*387G>A
NR_028033.4:n.982G>A
NR_028034.4:n.844G>A
NR_028035.4:n.907G>A
NR_028036.4:n.1045G>A
NR_135313.2:n.962G>A
NR_135314.2:n.1241G>A
NR_135315.2:n.994G>A