Canonical Allele Identifier: CA377510073

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774100G>T (hg19) ; chr10:g.89014343G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014343G>T , CM000672.2:g.89014343G>T	GRCh38
NC_000010.10:g.90774100G>T , CM000672.1:g.90774100G>T	GRCh37
NC_000010.9:g.90764080G>T	NCBI36
NG_009089.2:g.28813G>T , LRG_134:g.28813G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1210G>T
ENST00000355740.8:c.*224G>T	ENSP00000347979.3:n.*224G>T
ENST00000357339.7:c.838G>T	ENSP00000349896.2:p.Ala280Ser
ENST00000371857.8:n.2446G>T
ENST00000460510.6:c.184G>T	ENSP00000512812.1:p.Ala62Ser
ENST00000466081.6:n.2550G>T
ENST00000477270.6:c.946G>T	ENSP00000512813.1:p.Ala316Ser
ENST00000479522.6:c.*330G>T	ENSP00000424113.1:n.*330G>T
ENST00000484444.6:c.*342G>T	ENSP00000420975.1:n.*342G>T
ENST00000488877.6:c.792G>T	ENSP00000425159.1:n.792G>T
ENST00000492756.7:c.*330G>T	ENSP00000422453.1:n.*330G>T
ENST00000494799.6:c.184G>T	ENSP00000512834.1:p.Ala62Ser
ENST00000562983.3:c.184G>T	ENSP00000512845.1:p.Ala62Ser
ENST00000612663.6:c.*303G>T	ENSP00000477997.3:n.*303G>T
ENST00000640140.2:n.1046G>T
ENST00000640250.2:n.400G>T
ENST00000640681.2:n.1005G>T
ENST00000696723.1:n.4534G>T
ENST00000696741.1:n.2539G>T
ENST00000696742.1:n.2266G>T
ENST00000696743.1:n.3669G>T
ENST00000696744.1:n.940G>T
ENST00000696767.1:n.1235G>T
ENST00000696768.1:c.*224G>T	ENSP00000512859.1:n.*224G>T
ENST00000696769.1:n.2590G>T
ENST00000696771.1:c.184G>T	ENSP00000512860.1:p.Ala62Ser
ENST00000696772.1:n.2504G>T
ENST00000696773.1:n.2243G>T
ENST00000696774.1:n.6011G>T
ENST00000696776.1:c.994G>T	ENSP00000512861.1:p.Ala332Ser
ENST00000696777.1:n.2309G>T
ENST00000696778.1:n.1337G>T
ENST00000696779.1:c.508G>T	ENSP00000512862.1:p.Ala170Ser
ENST00000696780.1:c.931G>T	ENSP00000512863.1:p.Ala311Ser
ENST00000696781.1:c.646G>T	ENSP00000512864.1:p.Ala216Ser
ENST00000696782.1:c.*303G>T	ENSP00000512865.1:n.*303G>T
ENST00000696783.1:n.2769G>T
ENST00000696992.1:n.2018G>T
ENST00000696995.1:n.4430G>T
ENST00000696996.1:n.2343G>T
ENST00000696997.1:c.*531G>T	ENSP00000513028.1:n.*531G>T
ENST00000696998.1:n.2155G>T
ENST00000696999.1:c.184G>T	ENSP00000513029.1:p.Ala62Ser
ENST00000697036.1:c.*317G>T	ENSP00000513060.1:n.*317G>T
ENST00000697037.1:n.936G>T
ENST00000697093.1:n.3137G>T
ENST00000697094.1:n.3484G>T
ENST00000697095.1:c.*2102G>T	ENSP00000513104.1:n.*2102G>T
ENST00000697096.1:n.2034G>T
ENST00000697097.1:c.184G>T	ENSP00000513105.1:p.Ala62Ser
ENST00000562983.2:n.1087G>T
ENST00000690268.1:c.982G>T	ENSP00000509810.1:p.Ala328Ser
ENST00000355740.7:c.*227G>T	ENSP00000347979.3:n.*227G>T
ENST00000612663.5:c.*303G>T	ENSP00000477997.3:n.*303G>T
ENST00000640140.1:n.1073G>T
ENST00000640250.1:n.400G>T
ENST00000640681.1:n.1022G>T
ENST00000652046.1:c.901G>T MANE Select	ENSP00000498466.1:p.Ala301Ser
ENST00000352159.8:c.*218G>T	ENSP00000345601.4:n.*218G>T
ENST00000355279.2:c.876G>T	ENSP00000347426.2:n.876G>T
ENST00000355740.6:c.901G>T	ENSP00000347979.2:p.Ala301Ser
ENST00000357339.6:c.838G>T	ENSP00000349896.2:p.Ala280Ser
ENST00000479522.5:c.*330G>T	ENSP00000424113.1:n.*330G>T
ENST00000484444.5:c.*342G>T	ENSP00000420975.1:n.*342G>T
ENST00000488877.5:c.*342G>T	ENSP00000425159.1:n.*342G>T
ENST00000492756.5:c.729G>T	ENSP00000422453.1:n.729G>T
ENST00000494410.5:c.*259G>T	ENSP00000423755.1:n.*259G>T
ENST00000612663.4:c.*248G>T	ENSP00000477997.2:n.*248G>T
NM_000043.4:c.901G>T , LRG_134t1:c.901G>T	NP_000034.1:p.Ala301Ser
NM_152871.2:c.838G>T	NP_690610.1:p.Ala280Ser
NM_152872.2:c.*213G>T	NP_690611.1:n.*213G>T
NR_028033.2:n.1075G>T
NR_028034.2:n.937G>T
NR_028035.2:n.1000G>T
NR_028036.2:n.1138G>T
XM_006717819.2:c.982G>T	XP_006717882.1:p.Ala328Ser
XM_011539764.1:c.1063G>T	XP_011538066.1:p.Ala355Ser
XM_011539765.1:c.1000G>T	XP_011538067.1:p.Ala334Ser
XM_011539766.1:c.982G>T	XP_011538068.1:p.Ala328Ser
XM_011539767.1:c.946G>T	XP_011538069.1:p.Ala316Ser
XR_945732.1:n.969G>T
XR_945733.1:n.906G>T
NM_000043.5:c.901G>T	NP_000034.1:p.Ala301Ser
NM_001320619.1:c.*224G>T	NP_001307548.1:n.*224G>T
NM_152871.3:c.838G>T	NP_690610.1:p.Ala280Ser
NM_152872.3:c.*213G>T	NP_690611.1:n.*213G>T
NR_028033.3:n.1047G>T
NR_028034.3:n.909G>T
NR_028035.3:n.972G>T
NR_028036.3:n.1110G>T
NR_135313.1:n.1027G>T
NR_135314.1:n.1210G>T
NR_135315.1:n.963G>T
XM_006717819.3:c.982G>T	XP_006717882.1:p.Ala328Ser
XM_011539764.2:c.1063G>T	XP_011538066.1:p.Ala355Ser
XM_011539765.2:c.1000G>T	XP_011538067.1:p.Ala334Ser
XM_011539766.2:c.982G>T	XP_011538068.1:p.Ala328Ser
XM_011539767.3:c.946G>T	XP_011538069.1:p.Ala316Ser
XR_945732.3:n.969G>T
XR_945733.2:n.906G>T
NM_000043.6:c.901G>T MANE Select	NP_000034.1:p.Ala301Ser
NM_001320619.2:c.*224G>T	NP_001307548.1:n.*224G>T
NM_152871.4:c.838G>T	NP_690610.1:p.Ala280Ser
NM_152872.4:c.*213G>T	NP_690611.1:n.*213G>T
NR_028033.4:n.808G>T
NR_028034.4:n.670G>T
NR_028035.4:n.733G>T
NR_028036.4:n.871G>T
NR_135313.2:n.788G>T
NR_135314.2:n.1067G>T
NR_135315.2:n.820G>T