Canonical Allele Identifier: CA377509909

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774029T>C (hg19) ; chr10:g.89014272T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014272T>C , CM000672.2:g.89014272T>C	GRCh38
NC_000010.10:g.90774029T>C , CM000672.1:g.90774029T>C	GRCh37
NC_000010.9:g.90764009T>C	NCBI36
NG_009089.2:g.28742T>C , LRG_134:g.28742T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1139T>C
ENST00000355740.8:c.*153T>C	ENSP00000347979.3:n.*153T>C
ENST00000357339.7:c.767T>C	ENSP00000349896.2:p.Leu256Pro
ENST00000371857.8:n.2375T>C
ENST00000460510.6:c.113T>C	ENSP00000512812.1:p.Leu38Pro
ENST00000466081.6:n.2479T>C
ENST00000477270.6:c.875T>C	ENSP00000512813.1:p.Leu292Pro
ENST00000479522.6:c.*259T>C	ENSP00000424113.1:n.*259T>C
ENST00000484444.6:c.*271T>C	ENSP00000420975.1:n.*271T>C
ENST00000488877.6:c.721T>C	ENSP00000425159.1:n.721T>C
ENST00000492756.7:c.*259T>C	ENSP00000422453.1:n.*259T>C
ENST00000494799.6:c.113T>C	ENSP00000512834.1:p.Leu38Pro
ENST00000562983.3:c.113T>C	ENSP00000512845.1:p.Leu38Pro
ENST00000612663.6:c.*232T>C	ENSP00000477997.3:n.*232T>C
ENST00000640140.2:n.975T>C
ENST00000640250.2:n.329T>C
ENST00000640681.2:n.934T>C
ENST00000696723.1:n.4463T>C
ENST00000696741.1:n.2468T>C
ENST00000696742.1:n.2195T>C
ENST00000696743.1:n.3598T>C
ENST00000696744.1:n.869T>C
ENST00000696767.1:n.1164T>C
ENST00000696768.1:c.*153T>C	ENSP00000512859.1:n.*153T>C
ENST00000696769.1:n.2519T>C
ENST00000696771.1:c.113T>C	ENSP00000512860.1:p.Leu38Pro
ENST00000696772.1:n.2433T>C
ENST00000696773.1:n.2172T>C
ENST00000696774.1:n.5940T>C
ENST00000696776.1:c.923T>C	ENSP00000512861.1:p.Leu308Pro
ENST00000696777.1:n.2238T>C
ENST00000696778.1:n.1266T>C
ENST00000696779.1:c.437T>C	ENSP00000512862.1:p.Leu146Pro
ENST00000696780.1:c.860T>C	ENSP00000512863.1:p.Leu287Pro
ENST00000696781.1:c.575T>C	ENSP00000512864.1:p.Leu192Pro
ENST00000696782.1:c.*232T>C	ENSP00000512865.1:n.*232T>C
ENST00000696783.1:n.2698T>C
ENST00000696992.1:n.1947T>C
ENST00000696995.1:n.4359T>C
ENST00000696996.1:n.2272T>C
ENST00000696997.1:c.*460T>C	ENSP00000513028.1:n.*460T>C
ENST00000696998.1:n.2084T>C
ENST00000696999.1:c.113T>C	ENSP00000513029.1:p.Leu38Pro
ENST00000697035.1:c.*163T>C	ENSP00000513059.1:n.*163T>C
ENST00000697036.1:c.*246T>C	ENSP00000513060.1:n.*246T>C
ENST00000697037.1:n.865T>C
ENST00000697093.1:n.3066T>C
ENST00000697094.1:n.3413T>C
ENST00000697095.1:c.*2031T>C	ENSP00000513104.1:n.*2031T>C
ENST00000697096.1:n.1963T>C
ENST00000697097.1:c.113T>C	ENSP00000513105.1:p.Leu38Pro
ENST00000562983.2:n.1016T>C
ENST00000690268.1:c.911T>C	ENSP00000509810.1:p.Leu304Pro
ENST00000355740.7:c.*156T>C	ENSP00000347979.3:n.*156T>C
ENST00000612663.5:c.*232T>C	ENSP00000477997.3:n.*232T>C
ENST00000640140.1:n.1002T>C
ENST00000640250.1:n.329T>C
ENST00000640681.1:n.951T>C
ENST00000652046.1:c.830T>C MANE Select	ENSP00000498466.1:p.Leu277Pro
ENST00000352159.8:c.*147T>C	ENSP00000345601.4:n.*147T>C
ENST00000355279.2:c.805T>C	ENSP00000347426.2:n.805T>C
ENST00000355740.6:c.830T>C	ENSP00000347979.2:p.Leu277Pro
ENST00000357339.6:c.767T>C	ENSP00000349896.2:p.Leu256Pro
ENST00000479522.5:c.*259T>C	ENSP00000424113.1:n.*259T>C
ENST00000484444.5:c.*271T>C	ENSP00000420975.1:n.*271T>C
ENST00000488877.5:c.*271T>C	ENSP00000425159.1:n.*271T>C
ENST00000492756.5:c.658T>C	ENSP00000422453.1:n.658T>C
ENST00000494410.5:c.*188T>C	ENSP00000423755.1:n.*188T>C
ENST00000612663.4:c.*177T>C	ENSP00000477997.2:n.*177T>C
NM_000043.4:c.830T>C , LRG_134t1:c.830T>C	NP_000034.1:p.Leu277Pro
NM_152871.2:c.767T>C	NP_690610.1:p.Leu256Pro
NM_152872.2:c.*142T>C	NP_690611.1:n.*142T>C
NR_028033.2:n.1004T>C
NR_028034.2:n.866T>C
NR_028035.2:n.929T>C
NR_028036.2:n.1067T>C
XM_006717819.2:c.911T>C	XP_006717882.1:p.Leu304Pro
XM_011539764.1:c.992T>C	XP_011538066.1:p.Leu331Pro
XM_011539765.1:c.929T>C	XP_011538067.1:p.Leu310Pro
XM_011539766.1:c.911T>C	XP_011538068.1:p.Leu304Pro
XM_011539767.1:c.875T>C	XP_011538069.1:p.Leu292Pro
XR_945732.1:n.898T>C
XR_945733.1:n.835T>C
NM_000043.5:c.830T>C	NP_000034.1:p.Leu277Pro
NM_001320619.1:c.*153T>C	NP_001307548.1:n.*153T>C
NM_152871.3:c.767T>C	NP_690610.1:p.Leu256Pro
NM_152872.3:c.*142T>C	NP_690611.1:n.*142T>C
NR_028033.3:n.976T>C
NR_028034.3:n.838T>C
NR_028035.3:n.901T>C
NR_028036.3:n.1039T>C
NR_135313.1:n.956T>C
NR_135314.1:n.1139T>C
NR_135315.1:n.892T>C
XM_006717819.3:c.911T>C	XP_006717882.1:p.Leu304Pro
XM_011539764.2:c.992T>C	XP_011538066.1:p.Leu331Pro
XM_011539765.2:c.929T>C	XP_011538067.1:p.Leu310Pro
XM_011539766.2:c.911T>C	XP_011538068.1:p.Leu304Pro
XM_011539767.3:c.875T>C	XP_011538069.1:p.Leu292Pro
XR_945732.3:n.898T>C
XR_945733.2:n.835T>C
NM_000043.6:c.830T>C MANE Select	NP_000034.1:p.Leu277Pro
NM_001320619.2:c.*153T>C	NP_001307548.1:n.*153T>C
NM_152871.4:c.767T>C	NP_690610.1:p.Leu256Pro
NM_152872.4:c.*142T>C	NP_690611.1:n.*142T>C
NR_028033.4:n.737T>C
NR_028034.4:n.599T>C
NR_028035.4:n.662T>C
NR_028036.4:n.800T>C
NR_135313.2:n.717T>C
NR_135314.2:n.996T>C
NR_135315.2:n.749T>C