Canonical Allele Identifier: CA377510076

Gene: FAS

Linked Data

• dbSNP Id: rs2119447676
• MyVariant Identifiers: chr10:g.90774101C>T (hg19) ; chr10:g.89014344C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014344C>T , CM000672.2:g.89014344C>T	GRCh38
NC_000010.10:g.90774101C>T , CM000672.1:g.90774101C>T	GRCh37
NC_000010.9:g.90764081C>T	NCBI36
NG_009089.2:g.28814C>T , LRG_134:g.28814C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1211C>T
ENST00000355740.8:c.*225C>T	ENSP00000347979.3:n.*225C>T
ENST00000357339.7:c.839C>T	ENSP00000349896.2:p.Ala280Val
ENST00000371857.8:n.2447C>T
ENST00000460510.6:c.185C>T	ENSP00000512812.1:p.Ala62Val
ENST00000466081.6:n.2551C>T
ENST00000477270.6:c.947C>T	ENSP00000512813.1:p.Ala316Val
ENST00000479522.6:c.*331C>T	ENSP00000424113.1:n.*331C>T
ENST00000484444.6:c.*343C>T	ENSP00000420975.1:n.*343C>T
ENST00000488877.6:c.793C>T	ENSP00000425159.1:n.793C>T
ENST00000492756.7:c.*331C>T	ENSP00000422453.1:n.*331C>T
ENST00000494799.6:c.185C>T	ENSP00000512834.1:p.Ala62Val
ENST00000562983.3:c.185C>T	ENSP00000512845.1:p.Ala62Val
ENST00000612663.6:c.*304C>T	ENSP00000477997.3:n.*304C>T
ENST00000640140.2:n.1047C>T
ENST00000640250.2:n.401C>T
ENST00000640681.2:n.1006C>T
ENST00000696723.1:n.4535C>T
ENST00000696741.1:n.2540C>T
ENST00000696742.1:n.2267C>T
ENST00000696743.1:n.3670C>T
ENST00000696744.1:n.941C>T
ENST00000696767.1:n.1236C>T
ENST00000696768.1:c.*225C>T	ENSP00000512859.1:n.*225C>T
ENST00000696769.1:n.2591C>T
ENST00000696771.1:c.185C>T	ENSP00000512860.1:p.Ala62Val
ENST00000696772.1:n.2505C>T
ENST00000696773.1:n.2244C>T
ENST00000696774.1:n.6012C>T
ENST00000696776.1:c.995C>T	ENSP00000512861.1:p.Ala332Val
ENST00000696777.1:n.2310C>T
ENST00000696778.1:n.1338C>T
ENST00000696779.1:c.509C>T	ENSP00000512862.1:p.Ala170Val
ENST00000696780.1:c.932C>T	ENSP00000512863.1:p.Ala311Val
ENST00000696781.1:c.647C>T	ENSP00000512864.1:p.Ala216Val
ENST00000696782.1:c.*304C>T	ENSP00000512865.1:n.*304C>T
ENST00000696783.1:n.2770C>T
ENST00000696992.1:n.2019C>T
ENST00000696995.1:n.4431C>T
ENST00000696996.1:n.2344C>T
ENST00000696997.1:c.*532C>T	ENSP00000513028.1:n.*532C>T
ENST00000696998.1:n.2156C>T
ENST00000696999.1:c.185C>T	ENSP00000513029.1:p.Ala62Val
ENST00000697036.1:c.*318C>T	ENSP00000513060.1:n.*318C>T
ENST00000697037.1:n.937C>T
ENST00000697093.1:n.3138C>T
ENST00000697094.1:n.3485C>T
ENST00000697095.1:c.*2103C>T	ENSP00000513104.1:n.*2103C>T
ENST00000697096.1:n.2035C>T
ENST00000697097.1:c.185C>T	ENSP00000513105.1:p.Ala62Val
ENST00000562983.2:n.1088C>T
ENST00000690268.1:c.983C>T	ENSP00000509810.1:p.Ala328Val
ENST00000355740.7:c.*228C>T	ENSP00000347979.3:n.*228C>T
ENST00000612663.5:c.*304C>T	ENSP00000477997.3:n.*304C>T
ENST00000640140.1:n.1074C>T
ENST00000640250.1:n.401C>T
ENST00000640681.1:n.1023C>T
ENST00000652046.1:c.902C>T MANE Select	ENSP00000498466.1:p.Ala301Val
ENST00000352159.8:c.*219C>T	ENSP00000345601.4:n.*219C>T
ENST00000355279.2:c.877C>T	ENSP00000347426.2:n.877C>T
ENST00000355740.6:c.902C>T	ENSP00000347979.2:p.Ala301Val
ENST00000357339.6:c.839C>T	ENSP00000349896.2:p.Ala280Val
ENST00000479522.5:c.*331C>T	ENSP00000424113.1:n.*331C>T
ENST00000484444.5:c.*343C>T	ENSP00000420975.1:n.*343C>T
ENST00000488877.5:c.*343C>T	ENSP00000425159.1:n.*343C>T
ENST00000492756.5:c.730C>T	ENSP00000422453.1:n.730C>T
ENST00000494410.5:c.*260C>T	ENSP00000423755.1:n.*260C>T
ENST00000612663.4:c.*249C>T	ENSP00000477997.2:n.*249C>T
NM_000043.4:c.902C>T , LRG_134t1:c.902C>T	NP_000034.1:p.Ala301Val
NM_152871.2:c.839C>T	NP_690610.1:p.Ala280Val
NM_152872.2:c.*214C>T	NP_690611.1:n.*214C>T
NR_028033.2:n.1076C>T
NR_028034.2:n.938C>T
NR_028035.2:n.1001C>T
NR_028036.2:n.1139C>T
XM_006717819.2:c.983C>T	XP_006717882.1:p.Ala328Val
XM_011539764.1:c.1064C>T	XP_011538066.1:p.Ala355Val
XM_011539765.1:c.1001C>T	XP_011538067.1:p.Ala334Val
XM_011539766.1:c.983C>T	XP_011538068.1:p.Ala328Val
XM_011539767.1:c.947C>T	XP_011538069.1:p.Ala316Val
XR_945732.1:n.970C>T
XR_945733.1:n.907C>T
NM_000043.5:c.902C>T	NP_000034.1:p.Ala301Val
NM_001320619.1:c.*225C>T	NP_001307548.1:n.*225C>T
NM_152871.3:c.839C>T	NP_690610.1:p.Ala280Val
NM_152872.3:c.*214C>T	NP_690611.1:n.*214C>T
NR_028033.3:n.1048C>T
NR_028034.3:n.910C>T
NR_028035.3:n.973C>T
NR_028036.3:n.1111C>T
NR_135313.1:n.1028C>T
NR_135314.1:n.1211C>T
NR_135315.1:n.964C>T
XM_006717819.3:c.983C>T	XP_006717882.1:p.Ala328Val
XM_011539764.2:c.1064C>T	XP_011538066.1:p.Ala355Val
XM_011539765.2:c.1001C>T	XP_011538067.1:p.Ala334Val
XM_011539766.2:c.983C>T	XP_011538068.1:p.Ala328Val
XM_011539767.3:c.947C>T	XP_011538069.1:p.Ala316Val
XR_945732.3:n.970C>T
XR_945733.2:n.907C>T
NM_000043.6:c.902C>T MANE Select	NP_000034.1:p.Ala301Val
NM_001320619.2:c.*225C>T	NP_001307548.1:n.*225C>T
NM_152871.4:c.839C>T	NP_690610.1:p.Ala280Val
NM_152872.4:c.*214C>T	NP_690611.1:n.*214C>T
NR_028033.4:n.809C>T
NR_028034.4:n.671C>T
NR_028035.4:n.734C>T
NR_028036.4:n.872C>T
NR_135313.2:n.789C>T
NR_135314.2:n.1068C>T
NR_135315.2:n.821C>T