Canonical Allele Identifier: CA377510106

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774116T>C (hg19) ; chr10:g.89014359T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014359T>C , CM000672.2:g.89014359T>C	GRCh38
NC_000010.10:g.90774116T>C , CM000672.1:g.90774116T>C	GRCh37
NC_000010.9:g.90764096T>C	NCBI36
NG_009089.2:g.28829T>C , LRG_134:g.28829T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1226T>C
ENST00000355740.8:c.*240T>C	ENSP00000347979.3:n.*240T>C
ENST00000357339.7:c.854T>C	ENSP00000349896.2:p.Leu285Pro
ENST00000371857.8:n.2462T>C
ENST00000460510.6:c.200T>C	ENSP00000512812.1:p.Leu67Pro
ENST00000466081.6:n.2566T>C
ENST00000477270.6:c.962T>C	ENSP00000512813.1:p.Leu321Pro
ENST00000479522.6:c.*346T>C	ENSP00000424113.1:n.*346T>C
ENST00000484444.6:c.*358T>C	ENSP00000420975.1:n.*358T>C
ENST00000488877.6:c.808T>C	ENSP00000425159.1:n.808T>C
ENST00000492756.7:c.*346T>C	ENSP00000422453.1:n.*346T>C
ENST00000494799.6:c.200T>C	ENSP00000512834.1:p.Leu67Pro
ENST00000562983.3:c.200T>C	ENSP00000512845.1:p.Leu67Pro
ENST00000612663.6:c.*319T>C	ENSP00000477997.3:n.*319T>C
ENST00000640140.2:n.1062T>C
ENST00000640250.2:n.416T>C
ENST00000640681.2:n.1021T>C
ENST00000696723.1:n.4550T>C
ENST00000696741.1:n.2555T>C
ENST00000696742.1:n.2282T>C
ENST00000696743.1:n.3685T>C
ENST00000696744.1:n.956T>C
ENST00000696767.1:n.1251T>C
ENST00000696768.1:c.*240T>C	ENSP00000512859.1:n.*240T>C
ENST00000696769.1:n.2606T>C
ENST00000696771.1:c.200T>C	ENSP00000512860.1:p.Leu67Pro
ENST00000696772.1:n.2520T>C
ENST00000696773.1:n.2259T>C
ENST00000696774.1:n.6027T>C
ENST00000696776.1:c.1010T>C	ENSP00000512861.1:p.Leu337Pro
ENST00000696777.1:n.2325T>C
ENST00000696778.1:n.1353T>C
ENST00000696779.1:c.524T>C	ENSP00000512862.1:p.Leu175Pro
ENST00000696780.1:c.947T>C	ENSP00000512863.1:p.Leu316Pro
ENST00000696781.1:c.662T>C	ENSP00000512864.1:p.Leu221Pro
ENST00000696782.1:c.*319T>C	ENSP00000512865.1:n.*319T>C
ENST00000696783.1:n.2785T>C
ENST00000696992.1:n.2034T>C
ENST00000696995.1:n.4446T>C
ENST00000696996.1:n.2359T>C
ENST00000696997.1:c.*547T>C	ENSP00000513028.1:n.*547T>C
ENST00000696998.1:n.2171T>C
ENST00000696999.1:c.200T>C	ENSP00000513029.1:p.Leu67Pro
ENST00000697036.1:c.*333T>C	ENSP00000513060.1:n.*333T>C
ENST00000697037.1:n.952T>C
ENST00000697093.1:n.3153T>C
ENST00000697094.1:n.3500T>C
ENST00000697095.1:c.*2118T>C	ENSP00000513104.1:n.*2118T>C
ENST00000697096.1:n.2050T>C
ENST00000697097.1:c.200T>C	ENSP00000513105.1:p.Leu67Pro
ENST00000562983.2:n.1103T>C
ENST00000690268.1:c.998T>C	ENSP00000509810.1:p.Leu333Pro
ENST00000355740.7:c.*243T>C	ENSP00000347979.3:n.*243T>C
ENST00000612663.5:c.*319T>C	ENSP00000477997.3:n.*319T>C
ENST00000640140.1:n.1089T>C
ENST00000640250.1:n.416T>C
ENST00000640681.1:n.1038T>C
ENST00000652046.1:c.917T>C MANE Select	ENSP00000498466.1:p.Leu306Pro
ENST00000352159.8:c.*234T>C	ENSP00000345601.4:n.*234T>C
ENST00000355279.2:c.892T>C	ENSP00000347426.2:n.892T>C
ENST00000355740.6:c.917T>C	ENSP00000347979.2:p.Leu306Pro
ENST00000357339.6:c.854T>C	ENSP00000349896.2:p.Leu285Pro
ENST00000479522.5:c.*346T>C	ENSP00000424113.1:n.*346T>C
ENST00000484444.5:c.*358T>C	ENSP00000420975.1:n.*358T>C
ENST00000488877.5:c.*358T>C	ENSP00000425159.1:n.*358T>C
ENST00000492756.5:c.745T>C	ENSP00000422453.1:n.745T>C
ENST00000494410.5:c.*275T>C	ENSP00000423755.1:n.*275T>C
ENST00000612663.4:c.*264T>C	ENSP00000477997.2:n.*264T>C
NM_000043.4:c.917T>C , LRG_134t1:c.917T>C	NP_000034.1:p.Leu306Pro
NM_152871.2:c.854T>C	NP_690610.1:p.Leu285Pro
NM_152872.2:c.*229T>C	NP_690611.1:n.*229T>C
NR_028033.2:n.1091T>C
NR_028034.2:n.953T>C
NR_028035.2:n.1016T>C
NR_028036.2:n.1154T>C
XM_006717819.2:c.998T>C	XP_006717882.1:p.Leu333Pro
XM_011539764.1:c.1079T>C	XP_011538066.1:p.Leu360Pro
XM_011539765.1:c.1016T>C	XP_011538067.1:p.Leu339Pro
XM_011539766.1:c.998T>C	XP_011538068.1:p.Leu333Pro
XM_011539767.1:c.962T>C	XP_011538069.1:p.Leu321Pro
XR_945732.1:n.985T>C
XR_945733.1:n.922T>C
NM_000043.5:c.917T>C	NP_000034.1:p.Leu306Pro
NM_001320619.1:c.*240T>C	NP_001307548.1:n.*240T>C
NM_152871.3:c.854T>C	NP_690610.1:p.Leu285Pro
NM_152872.3:c.*229T>C	NP_690611.1:n.*229T>C
NR_028033.3:n.1063T>C
NR_028034.3:n.925T>C
NR_028035.3:n.988T>C
NR_028036.3:n.1126T>C
NR_135313.1:n.1043T>C
NR_135314.1:n.1226T>C
NR_135315.1:n.979T>C
XM_006717819.3:c.998T>C	XP_006717882.1:p.Leu333Pro
XM_011539764.2:c.1079T>C	XP_011538066.1:p.Leu360Pro
XM_011539765.2:c.1016T>C	XP_011538067.1:p.Leu339Pro
XM_011539766.2:c.998T>C	XP_011538068.1:p.Leu333Pro
XM_011539767.3:c.962T>C	XP_011538069.1:p.Leu321Pro
XR_945732.3:n.985T>C
XR_945733.2:n.922T>C
NM_000043.6:c.917T>C MANE Select	NP_000034.1:p.Leu306Pro
NM_001320619.2:c.*240T>C	NP_001307548.1:n.*240T>C
NM_152871.4:c.854T>C	NP_690610.1:p.Leu285Pro
NM_152872.4:c.*229T>C	NP_690611.1:n.*229T>C
NR_028033.4:n.824T>C
NR_028034.4:n.686T>C
NR_028035.4:n.749T>C
NR_028036.4:n.887T>C
NR_135313.2:n.804T>C
NR_135314.2:n.1083T>C
NR_135315.2:n.836T>C