Canonical Allele Identifier: CA377510079

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774103A>T (hg19) ; chr10:g.89014346A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014346A>T , CM000672.2:g.89014346A>T	GRCh38
NC_000010.10:g.90774103A>T , CM000672.1:g.90774103A>T	GRCh37
NC_000010.9:g.90764083A>T	NCBI36
NG_009089.2:g.28816A>T , LRG_134:g.28816A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1213A>T
ENST00000355740.8:c.*227A>T	ENSP00000347979.3:n.*227A>T
ENST00000357339.7:c.841A>T	ENSP00000349896.2:p.Asn281Tyr
ENST00000371857.8:n.2449A>T
ENST00000460510.6:c.187A>T	ENSP00000512812.1:p.Asn63Tyr
ENST00000466081.6:n.2553A>T
ENST00000477270.6:c.949A>T	ENSP00000512813.1:p.Asn317Tyr
ENST00000479522.6:c.*333A>T	ENSP00000424113.1:n.*333A>T
ENST00000484444.6:c.*345A>T	ENSP00000420975.1:n.*345A>T
ENST00000488877.6:c.795A>T	ENSP00000425159.1:n.795A>T
ENST00000492756.7:c.*333A>T	ENSP00000422453.1:n.*333A>T
ENST00000494799.6:c.187A>T	ENSP00000512834.1:p.Asn63Tyr
ENST00000562983.3:c.187A>T	ENSP00000512845.1:p.Asn63Tyr
ENST00000612663.6:c.*306A>T	ENSP00000477997.3:n.*306A>T
ENST00000640140.2:n.1049A>T
ENST00000640250.2:n.403A>T
ENST00000640681.2:n.1008A>T
ENST00000696723.1:n.4537A>T
ENST00000696741.1:n.2542A>T
ENST00000696742.1:n.2269A>T
ENST00000696743.1:n.3672A>T
ENST00000696744.1:n.943A>T
ENST00000696767.1:n.1238A>T
ENST00000696768.1:c.*227A>T	ENSP00000512859.1:n.*227A>T
ENST00000696769.1:n.2593A>T
ENST00000696771.1:c.187A>T	ENSP00000512860.1:p.Asn63Tyr
ENST00000696772.1:n.2507A>T
ENST00000696773.1:n.2246A>T
ENST00000696774.1:n.6014A>T
ENST00000696776.1:c.997A>T	ENSP00000512861.1:p.Asn333Tyr
ENST00000696777.1:n.2312A>T
ENST00000696778.1:n.1340A>T
ENST00000696779.1:c.511A>T	ENSP00000512862.1:p.Asn171Tyr
ENST00000696780.1:c.934A>T	ENSP00000512863.1:p.Asn312Tyr
ENST00000696781.1:c.649A>T	ENSP00000512864.1:p.Asn217Tyr
ENST00000696782.1:c.*306A>T	ENSP00000512865.1:n.*306A>T
ENST00000696783.1:n.2772A>T
ENST00000696992.1:n.2021A>T
ENST00000696995.1:n.4433A>T
ENST00000696996.1:n.2346A>T
ENST00000696997.1:c.*534A>T	ENSP00000513028.1:n.*534A>T
ENST00000696998.1:n.2158A>T
ENST00000696999.1:c.187A>T	ENSP00000513029.1:p.Asn63Tyr
ENST00000697036.1:c.*320A>T	ENSP00000513060.1:n.*320A>T
ENST00000697037.1:n.939A>T
ENST00000697093.1:n.3140A>T
ENST00000697094.1:n.3487A>T
ENST00000697095.1:c.*2105A>T	ENSP00000513104.1:n.*2105A>T
ENST00000697096.1:n.2037A>T
ENST00000697097.1:c.187A>T	ENSP00000513105.1:p.Asn63Tyr
ENST00000562983.2:n.1090A>T
ENST00000690268.1:c.985A>T	ENSP00000509810.1:p.Asn329Tyr
ENST00000355740.7:c.*230A>T	ENSP00000347979.3:n.*230A>T
ENST00000612663.5:c.*306A>T	ENSP00000477997.3:n.*306A>T
ENST00000640140.1:n.1076A>T
ENST00000640250.1:n.403A>T
ENST00000640681.1:n.1025A>T
ENST00000652046.1:c.904A>T MANE Select	ENSP00000498466.1:p.Asn302Tyr
ENST00000352159.8:c.*221A>T	ENSP00000345601.4:n.*221A>T
ENST00000355279.2:c.879A>T	ENSP00000347426.2:n.879A>T
ENST00000355740.6:c.904A>T	ENSP00000347979.2:p.Asn302Tyr
ENST00000357339.6:c.841A>T	ENSP00000349896.2:p.Asn281Tyr
ENST00000479522.5:c.*333A>T	ENSP00000424113.1:n.*333A>T
ENST00000484444.5:c.*345A>T	ENSP00000420975.1:n.*345A>T
ENST00000488877.5:c.*345A>T	ENSP00000425159.1:n.*345A>T
ENST00000492756.5:c.732A>T	ENSP00000422453.1:n.732A>T
ENST00000494410.5:c.*262A>T	ENSP00000423755.1:n.*262A>T
ENST00000612663.4:c.*251A>T	ENSP00000477997.2:n.*251A>T
NM_000043.4:c.904A>T , LRG_134t1:c.904A>T	NP_000034.1:p.Asn302Tyr
NM_152871.2:c.841A>T	NP_690610.1:p.Asn281Tyr
NM_152872.2:c.*216A>T	NP_690611.1:n.*216A>T
NR_028033.2:n.1078A>T
NR_028034.2:n.940A>T
NR_028035.2:n.1003A>T
NR_028036.2:n.1141A>T
XM_006717819.2:c.985A>T	XP_006717882.1:p.Asn329Tyr
XM_011539764.1:c.1066A>T	XP_011538066.1:p.Asn356Tyr
XM_011539765.1:c.1003A>T	XP_011538067.1:p.Asn335Tyr
XM_011539766.1:c.985A>T	XP_011538068.1:p.Asn329Tyr
XM_011539767.1:c.949A>T	XP_011538069.1:p.Asn317Tyr
XR_945732.1:n.972A>T
XR_945733.1:n.909A>T
NM_000043.5:c.904A>T	NP_000034.1:p.Asn302Tyr
NM_001320619.1:c.*227A>T	NP_001307548.1:n.*227A>T
NM_152871.3:c.841A>T	NP_690610.1:p.Asn281Tyr
NM_152872.3:c.*216A>T	NP_690611.1:n.*216A>T
NR_028033.3:n.1050A>T
NR_028034.3:n.912A>T
NR_028035.3:n.975A>T
NR_028036.3:n.1113A>T
NR_135313.1:n.1030A>T
NR_135314.1:n.1213A>T
NR_135315.1:n.966A>T
XM_006717819.3:c.985A>T	XP_006717882.1:p.Asn329Tyr
XM_011539764.2:c.1066A>T	XP_011538066.1:p.Asn356Tyr
XM_011539765.2:c.1003A>T	XP_011538067.1:p.Asn335Tyr
XM_011539766.2:c.985A>T	XP_011538068.1:p.Asn329Tyr
XM_011539767.3:c.949A>T	XP_011538069.1:p.Asn317Tyr
XR_945732.3:n.972A>T
XR_945733.2:n.909A>T
NM_000043.6:c.904A>T MANE Select	NP_000034.1:p.Asn302Tyr
NM_001320619.2:c.*227A>T	NP_001307548.1:n.*227A>T
NM_152871.4:c.841A>T	NP_690610.1:p.Asn281Tyr
NM_152872.4:c.*216A>T	NP_690611.1:n.*216A>T
NR_028033.4:n.811A>T
NR_028034.4:n.673A>T
NR_028035.4:n.736A>T
NR_028036.4:n.874A>T
NR_135313.2:n.791A>T
NR_135314.2:n.1070A>T
NR_135315.2:n.823A>T