Canonical Allele Identifier: CA377510045

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774089A>C (hg19) ; chr10:g.89014332A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014332A>C , CM000672.2:g.89014332A>C	GRCh38
NC_000010.10:g.90774089A>C , CM000672.1:g.90774089A>C	GRCh37
NC_000010.9:g.90764069A>C	NCBI36
NG_009089.2:g.28802A>C , LRG_134:g.28802A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1199A>C
ENST00000355740.8:c.*213A>C	ENSP00000347979.3:n.*213A>C
ENST00000357339.7:c.827A>C	ENSP00000349896.2:p.Asp276Ala
ENST00000371857.8:n.2435A>C
ENST00000460510.6:c.173A>C	ENSP00000512812.1:p.Asp58Ala
ENST00000466081.6:n.2539A>C
ENST00000477270.6:c.935A>C	ENSP00000512813.1:p.Asp312Ala
ENST00000479522.6:c.*319A>C	ENSP00000424113.1:n.*319A>C
ENST00000484444.6:c.*331A>C	ENSP00000420975.1:n.*331A>C
ENST00000488877.6:c.781A>C	ENSP00000425159.1:n.781A>C
ENST00000492756.7:c.*319A>C	ENSP00000422453.1:n.*319A>C
ENST00000494799.6:c.173A>C	ENSP00000512834.1:p.Asp58Ala
ENST00000562983.3:c.173A>C	ENSP00000512845.1:p.Asp58Ala
ENST00000612663.6:c.*292A>C	ENSP00000477997.3:n.*292A>C
ENST00000640140.2:n.1035A>C
ENST00000640250.2:n.389A>C
ENST00000640681.2:n.994A>C
ENST00000696723.1:n.4523A>C
ENST00000696741.1:n.2528A>C
ENST00000696742.1:n.2255A>C
ENST00000696743.1:n.3658A>C
ENST00000696744.1:n.929A>C
ENST00000696767.1:n.1224A>C
ENST00000696768.1:c.*213A>C	ENSP00000512859.1:n.*213A>C
ENST00000696769.1:n.2579A>C
ENST00000696771.1:c.173A>C	ENSP00000512860.1:p.Asp58Ala
ENST00000696772.1:n.2493A>C
ENST00000696773.1:n.2232A>C
ENST00000696774.1:n.6000A>C
ENST00000696776.1:c.983A>C	ENSP00000512861.1:p.Asp328Ala
ENST00000696777.1:n.2298A>C
ENST00000696778.1:n.1326A>C
ENST00000696779.1:c.497A>C	ENSP00000512862.1:p.Asp166Ala
ENST00000696780.1:c.920A>C	ENSP00000512863.1:p.Asp307Ala
ENST00000696781.1:c.635A>C	ENSP00000512864.1:p.Asp212Ala
ENST00000696782.1:c.*292A>C	ENSP00000512865.1:n.*292A>C
ENST00000696783.1:n.2758A>C
ENST00000696992.1:n.2007A>C
ENST00000696995.1:n.4419A>C
ENST00000696996.1:n.2332A>C
ENST00000696997.1:c.*520A>C	ENSP00000513028.1:n.*520A>C
ENST00000696998.1:n.2144A>C
ENST00000696999.1:c.173A>C	ENSP00000513029.1:p.Asp58Ala
ENST00000697036.1:c.*306A>C	ENSP00000513060.1:n.*306A>C
ENST00000697037.1:n.925A>C
ENST00000697093.1:n.3126A>C
ENST00000697094.1:n.3473A>C
ENST00000697095.1:c.*2091A>C	ENSP00000513104.1:n.*2091A>C
ENST00000697096.1:n.2023A>C
ENST00000697097.1:c.173A>C	ENSP00000513105.1:p.Asp58Ala
ENST00000562983.2:n.1076A>C
ENST00000690268.1:c.971A>C	ENSP00000509810.1:p.Asp324Ala
ENST00000355740.7:c.*216A>C	ENSP00000347979.3:n.*216A>C
ENST00000612663.5:c.*292A>C	ENSP00000477997.3:n.*292A>C
ENST00000640140.1:n.1062A>C
ENST00000640250.1:n.389A>C
ENST00000640681.1:n.1011A>C
ENST00000652046.1:c.890A>C MANE Select	ENSP00000498466.1:p.Asp297Ala
ENST00000352159.8:c.*207A>C	ENSP00000345601.4:n.*207A>C
ENST00000355279.2:c.865A>C	ENSP00000347426.2:n.865A>C
ENST00000355740.6:c.890A>C	ENSP00000347979.2:p.Asp297Ala
ENST00000357339.6:c.827A>C	ENSP00000349896.2:p.Asp276Ala
ENST00000479522.5:c.*319A>C	ENSP00000424113.1:n.*319A>C
ENST00000484444.5:c.*331A>C	ENSP00000420975.1:n.*331A>C
ENST00000488877.5:c.*331A>C	ENSP00000425159.1:n.*331A>C
ENST00000492756.5:c.718A>C	ENSP00000422453.1:n.718A>C
ENST00000494410.5:c.*248A>C	ENSP00000423755.1:n.*248A>C
ENST00000612663.4:c.*237A>C	ENSP00000477997.2:n.*237A>C
NM_000043.4:c.890A>C , LRG_134t1:c.890A>C	NP_000034.1:p.Asp297Ala
NM_152871.2:c.827A>C	NP_690610.1:p.Asp276Ala
NM_152872.2:c.*202A>C	NP_690611.1:n.*202A>C
NR_028033.2:n.1064A>C
NR_028034.2:n.926A>C
NR_028035.2:n.989A>C
NR_028036.2:n.1127A>C
XM_006717819.2:c.971A>C	XP_006717882.1:p.Asp324Ala
XM_011539764.1:c.1052A>C	XP_011538066.1:p.Asp351Ala
XM_011539765.1:c.989A>C	XP_011538067.1:p.Asp330Ala
XM_011539766.1:c.971A>C	XP_011538068.1:p.Asp324Ala
XM_011539767.1:c.935A>C	XP_011538069.1:p.Asp312Ala
XR_945732.1:n.958A>C
XR_945733.1:n.895A>C
NM_000043.5:c.890A>C	NP_000034.1:p.Asp297Ala
NM_001320619.1:c.*213A>C	NP_001307548.1:n.*213A>C
NM_152871.3:c.827A>C	NP_690610.1:p.Asp276Ala
NM_152872.3:c.*202A>C	NP_690611.1:n.*202A>C
NR_028033.3:n.1036A>C
NR_028034.3:n.898A>C
NR_028035.3:n.961A>C
NR_028036.3:n.1099A>C
NR_135313.1:n.1016A>C
NR_135314.1:n.1199A>C
NR_135315.1:n.952A>C
XM_006717819.3:c.971A>C	XP_006717882.1:p.Asp324Ala
XM_011539764.2:c.1052A>C	XP_011538066.1:p.Asp351Ala
XM_011539765.2:c.989A>C	XP_011538067.1:p.Asp330Ala
XM_011539766.2:c.971A>C	XP_011538068.1:p.Asp324Ala
XM_011539767.3:c.935A>C	XP_011538069.1:p.Asp312Ala
XR_945732.3:n.958A>C
XR_945733.2:n.895A>C
NM_000043.6:c.890A>C MANE Select	NP_000034.1:p.Asp297Ala
NM_001320619.2:c.*213A>C	NP_001307548.1:n.*213A>C
NM_152871.4:c.827A>C	NP_690610.1:p.Asp276Ala
NM_152872.4:c.*202A>C	NP_690611.1:n.*202A>C
NR_028033.4:n.797A>C
NR_028034.4:n.659A>C
NR_028035.4:n.722A>C
NR_028036.4:n.860A>C
NR_135313.2:n.777A>C
NR_135314.2:n.1056A>C
NR_135315.2:n.809A>C