Canonical Allele Identifier: CA377509721

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773953A>C (hg19) ; chr10:g.89014196A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014196A>C , CM000672.2:g.89014196A>C	GRCh38
NC_000010.10:g.90773953A>C , CM000672.1:g.90773953A>C	GRCh37
NC_000010.9:g.90763933A>C	NCBI36
NG_009089.2:g.28666A>C , LRG_134:g.28666A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1063A>C
ENST00000355740.8:c.*77A>C	ENSP00000347979.3:n.*77A>C
ENST00000357339.7:c.691A>C	ENSP00000349896.2:p.Asn231His
ENST00000371857.8:n.2299A>C
ENST00000460510.6:c.37A>C	ENSP00000512812.1:p.Asn13His
ENST00000466081.6:n.2403A>C
ENST00000477270.6:c.799A>C	ENSP00000512813.1:p.Asn267His
ENST00000479522.6:c.*183A>C	ENSP00000424113.1:n.*183A>C
ENST00000484444.6:c.*195A>C	ENSP00000420975.1:n.*195A>C
ENST00000488877.6:c.645A>C	ENSP00000425159.1:n.645A>C
ENST00000492756.7:c.*183A>C	ENSP00000422453.1:n.*183A>C
ENST00000494799.6:c.37A>C	ENSP00000512834.1:p.Asn13His
ENST00000562983.3:c.37A>C	ENSP00000512845.1:p.Asn13His
ENST00000612663.6:c.*156A>C	ENSP00000477997.3:n.*156A>C
ENST00000640140.2:n.899A>C
ENST00000640250.2:n.253A>C
ENST00000640681.2:n.858A>C
ENST00000696723.1:n.4387A>C
ENST00000696741.1:n.2392A>C
ENST00000696742.1:n.2119A>C
ENST00000696743.1:n.3522A>C
ENST00000696744.1:n.793A>C
ENST00000696767.1:n.1088A>C
ENST00000696768.1:c.*77A>C	ENSP00000512859.1:n.*77A>C
ENST00000696769.1:n.2443A>C
ENST00000696771.1:c.37A>C	ENSP00000512860.1:p.Asn13His
ENST00000696772.1:n.2357A>C
ENST00000696773.1:n.2096A>C
ENST00000696774.1:n.5864A>C
ENST00000696776.1:c.847A>C	ENSP00000512861.1:p.Asn283His
ENST00000696777.1:n.2162A>C
ENST00000696778.1:n.1190A>C
ENST00000696779.1:c.361A>C	ENSP00000512862.1:p.Asn121His
ENST00000696780.1:c.784A>C	ENSP00000512863.1:p.Asn262His
ENST00000696781.1:c.499A>C	ENSP00000512864.1:p.Asn167His
ENST00000696782.1:c.*156A>C	ENSP00000512865.1:n.*156A>C
ENST00000696783.1:n.2622A>C
ENST00000696992.1:n.1871A>C
ENST00000696995.1:n.4283A>C
ENST00000696996.1:n.2196A>C
ENST00000696997.1:c.*384A>C	ENSP00000513028.1:n.*384A>C
ENST00000696998.1:n.2008A>C
ENST00000696999.1:c.37A>C	ENSP00000513029.1:p.Asn13His
ENST00000697035.1:c.*87A>C	ENSP00000513059.1:n.*87A>C
ENST00000697036.1:c.*170A>C	ENSP00000513060.1:n.*170A>C
ENST00000697037.1:n.789A>C
ENST00000697093.1:n.2990A>C
ENST00000697094.1:n.3337A>C
ENST00000697095.1:c.*1955A>C	ENSP00000513104.1:n.*1955A>C
ENST00000697096.1:n.1887A>C
ENST00000697097.1:c.37A>C	ENSP00000513105.1:p.Asn13His
ENST00000562983.2:n.940A>C
ENST00000690268.1:c.835A>C	ENSP00000509810.1:p.Asn279His
ENST00000355740.7:c.*80A>C	ENSP00000347979.3:n.*80A>C
ENST00000612663.5:c.*156A>C	ENSP00000477997.3:n.*156A>C
ENST00000640140.1:n.926A>C
ENST00000640250.1:n.253A>C
ENST00000640681.1:n.875A>C
ENST00000652046.1:c.754A>C MANE Select	ENSP00000498466.1:p.Asn252His
ENST00000352159.8:c.*71A>C	ENSP00000345601.4:n.*71A>C
ENST00000355279.2:c.729A>C	ENSP00000347426.2:n.729A>C
ENST00000355740.6:c.754A>C	ENSP00000347979.2:p.Asn252His
ENST00000357339.6:c.691A>C	ENSP00000349896.2:p.Asn231His
ENST00000479522.5:c.*183A>C	ENSP00000424113.1:n.*183A>C
ENST00000484444.5:c.*195A>C	ENSP00000420975.1:n.*195A>C
ENST00000488877.5:c.*195A>C	ENSP00000425159.1:n.*195A>C
ENST00000492756.5:c.582A>C	ENSP00000422453.1:n.582A>C
ENST00000494410.5:c.*112A>C	ENSP00000423755.1:n.*112A>C
ENST00000494799.5:n.661A>C
ENST00000612663.4:c.*101A>C	ENSP00000477997.2:n.*101A>C
ENST00000615406.4:c.752A>C	ENSP00000484575.1:p.Glu251Ala
NM_000043.4:c.754A>C , LRG_134t1:c.754A>C	NP_000034.1:p.Asn252His
NM_152871.2:c.691A>C	NP_690610.1:p.Asn231His
NM_152872.2:c.*66A>C	NP_690611.1:n.*66A>C
NR_028033.2:n.928A>C
NR_028034.2:n.790A>C
NR_028035.2:n.853A>C
NR_028036.2:n.991A>C
XM_006717819.2:c.835A>C	XP_006717882.1:p.Asn279His
XM_011539764.1:c.916A>C	XP_011538066.1:p.Asn306His
XM_011539765.1:c.853A>C	XP_011538067.1:p.Asn285His
XM_011539766.1:c.835A>C	XP_011538068.1:p.Asn279His
XM_011539767.1:c.799A>C	XP_011538069.1:p.Asn267His
XR_945732.1:n.822A>C
XR_945733.1:n.759A>C
NM_000043.5:c.754A>C	NP_000034.1:p.Asn252His
NM_001320619.1:c.*77A>C	NP_001307548.1:n.*77A>C
NM_152871.3:c.691A>C	NP_690610.1:p.Asn231His
NM_152872.3:c.*66A>C	NP_690611.1:n.*66A>C
NR_028033.3:n.900A>C
NR_028034.3:n.762A>C
NR_028035.3:n.825A>C
NR_028036.3:n.963A>C
NR_135313.1:n.880A>C
NR_135314.1:n.1063A>C
NR_135315.1:n.816A>C
XM_006717819.3:c.835A>C	XP_006717882.1:p.Asn279His
XM_011539764.2:c.916A>C	XP_011538066.1:p.Asn306His
XM_011539765.2:c.853A>C	XP_011538067.1:p.Asn285His
XM_011539766.2:c.835A>C	XP_011538068.1:p.Asn279His
XM_011539767.3:c.799A>C	XP_011538069.1:p.Asn267His
XR_945732.3:n.822A>C
XR_945733.2:n.759A>C
NM_000043.6:c.754A>C MANE Select	NP_000034.1:p.Asn252His
NM_001320619.2:c.*77A>C	NP_001307548.1:n.*77A>C
NM_152871.4:c.691A>C	NP_690610.1:p.Asn231His
NM_152872.4:c.*66A>C	NP_690611.1:n.*66A>C
NR_028033.4:n.661A>C
NR_028034.4:n.523A>C
NR_028035.4:n.586A>C
NR_028036.4:n.724A>C
NR_135313.2:n.641A>C
NR_135314.2:n.920A>C
NR_135315.2:n.673A>C