Canonical Allele Identifier: CA377509687

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773936A>C (hg19) ; chr10:g.89014179A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014179A>C , CM000672.2:g.89014179A>C	GRCh38
NC_000010.10:g.90773936A>C , CM000672.1:g.90773936A>C	GRCh37
NC_000010.9:g.90763916A>C	NCBI36
NG_009089.2:g.28649A>C , LRG_134:g.28649A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1046A>C
ENST00000355740.8:c.*60A>C	ENSP00000347979.3:n.*60A>C
ENST00000357339.7:c.674A>C	ENSP00000349896.2:p.Lys225Thr
ENST00000371857.8:n.2282A>C
ENST00000460510.6:c.20A>C	ENSP00000512812.1:p.Lys7Thr
ENST00000466081.6:n.2386A>C
ENST00000477270.6:c.782A>C	ENSP00000512813.1:p.Lys261Thr
ENST00000479522.6:c.*166A>C	ENSP00000424113.1:n.*166A>C
ENST00000484444.6:c.*178A>C	ENSP00000420975.1:n.*178A>C
ENST00000488877.6:c.628A>C	ENSP00000425159.1:n.628A>C
ENST00000492756.7:c.*166A>C	ENSP00000422453.1:n.*166A>C
ENST00000494799.6:c.20A>C	ENSP00000512834.1:p.Lys7Thr
ENST00000562983.3:c.20A>C	ENSP00000512845.1:p.Lys7Thr
ENST00000612663.6:c.*139A>C	ENSP00000477997.3:n.*139A>C
ENST00000640140.2:n.882A>C
ENST00000640250.2:n.236A>C
ENST00000640681.2:n.841A>C
ENST00000696723.1:n.4370A>C
ENST00000696741.1:n.2375A>C
ENST00000696742.1:n.2102A>C
ENST00000696743.1:n.3505A>C
ENST00000696744.1:n.776A>C
ENST00000696767.1:n.1071A>C
ENST00000696768.1:c.*60A>C	ENSP00000512859.1:n.*60A>C
ENST00000696769.1:n.2426A>C
ENST00000696771.1:c.20A>C	ENSP00000512860.1:p.Lys7Thr
ENST00000696772.1:n.2340A>C
ENST00000696773.1:n.2079A>C
ENST00000696774.1:n.5847A>C
ENST00000696776.1:c.830A>C	ENSP00000512861.1:p.Lys277Thr
ENST00000696777.1:n.2145A>C
ENST00000696778.1:n.1173A>C
ENST00000696779.1:c.344A>C	ENSP00000512862.1:p.Lys115Thr
ENST00000696780.1:c.767A>C	ENSP00000512863.1:p.Lys256Thr
ENST00000696781.1:c.482A>C	ENSP00000512864.1:p.Lys161Thr
ENST00000696782.1:c.*139A>C	ENSP00000512865.1:n.*139A>C
ENST00000696783.1:n.2605A>C
ENST00000696992.1:n.1854A>C
ENST00000696995.1:n.4266A>C
ENST00000696996.1:n.2179A>C
ENST00000696997.1:c.*367A>C	ENSP00000513028.1:n.*367A>C
ENST00000696998.1:n.1991A>C
ENST00000696999.1:c.20A>C	ENSP00000513029.1:p.Lys7Thr
ENST00000697035.1:c.*70A>C	ENSP00000513059.1:n.*70A>C
ENST00000697036.1:c.*153A>C	ENSP00000513060.1:n.*153A>C
ENST00000697037.1:n.772A>C
ENST00000697093.1:n.2973A>C
ENST00000697094.1:n.3320A>C
ENST00000697095.1:c.*1938A>C	ENSP00000513104.1:n.*1938A>C
ENST00000697096.1:n.1870A>C
ENST00000697097.1:c.20A>C	ENSP00000513105.1:p.Lys7Thr
ENST00000562983.2:n.923A>C
ENST00000690268.1:c.818A>C	ENSP00000509810.1:p.Lys273Thr
ENST00000355740.7:c.*63A>C	ENSP00000347979.3:n.*63A>C
ENST00000612663.5:c.*139A>C	ENSP00000477997.3:n.*139A>C
ENST00000640140.1:n.909A>C
ENST00000640250.1:n.236A>C
ENST00000640681.1:n.858A>C
ENST00000652046.1:c.737A>C MANE Select	ENSP00000498466.1:p.Lys246Thr
ENST00000352159.8:c.*54A>C	ENSP00000345601.4:n.*54A>C
ENST00000355279.2:c.712A>C	ENSP00000347426.2:n.712A>C
ENST00000355740.6:c.737A>C	ENSP00000347979.2:p.Lys246Thr
ENST00000357339.6:c.674A>C	ENSP00000349896.2:p.Lys225Thr
ENST00000479522.5:c.*166A>C	ENSP00000424113.1:n.*166A>C
ENST00000484444.5:c.*178A>C	ENSP00000420975.1:n.*178A>C
ENST00000488877.5:c.*178A>C	ENSP00000425159.1:n.*178A>C
ENST00000492756.5:c.565A>C	ENSP00000422453.1:n.565A>C
ENST00000494410.5:c.*95A>C	ENSP00000423755.1:n.*95A>C
ENST00000494799.5:n.644A>C
ENST00000612663.4:c.*84A>C	ENSP00000477997.2:n.*84A>C
ENST00000615406.4:c.737A>C	ENSP00000484575.1:p.Lys246Thr
ENST00000626542.2:c.735A>C	ENSP00000485876.1:p.Ter245Tyr
NM_000043.4:c.737A>C , LRG_134t1:c.737A>C	NP_000034.1:p.Lys246Thr
NM_152871.2:c.674A>C	NP_690610.1:p.Lys225Thr
NM_152872.2:c.*49A>C	NP_690611.1:n.*49A>C
NR_028033.2:n.911A>C
NR_028034.2:n.773A>C
NR_028035.2:n.836A>C
NR_028036.2:n.974A>C
XM_006717819.2:c.818A>C	XP_006717882.1:p.Lys273Thr
XM_011539764.1:c.899A>C	XP_011538066.1:p.Lys300Thr
XM_011539765.1:c.836A>C	XP_011538067.1:p.Lys279Thr
XM_011539766.1:c.818A>C	XP_011538068.1:p.Lys273Thr
XM_011539767.1:c.782A>C	XP_011538069.1:p.Lys261Thr
XR_945732.1:n.805A>C
XR_945733.1:n.742A>C
NM_000043.5:c.737A>C	NP_000034.1:p.Lys246Thr
NM_001320619.1:c.*60A>C	NP_001307548.1:n.*60A>C
NM_152871.3:c.674A>C	NP_690610.1:p.Lys225Thr
NM_152872.3:c.*49A>C	NP_690611.1:n.*49A>C
NR_028033.3:n.883A>C
NR_028034.3:n.745A>C
NR_028035.3:n.808A>C
NR_028036.3:n.946A>C
NR_135313.1:n.863A>C
NR_135314.1:n.1046A>C
NR_135315.1:n.799A>C
XM_006717819.3:c.818A>C	XP_006717882.1:p.Lys273Thr
XM_011539764.2:c.899A>C	XP_011538066.1:p.Lys300Thr
XM_011539765.2:c.836A>C	XP_011538067.1:p.Lys279Thr
XM_011539766.2:c.818A>C	XP_011538068.1:p.Lys273Thr
XM_011539767.3:c.782A>C	XP_011538069.1:p.Lys261Thr
XR_945732.3:n.805A>C
XR_945733.2:n.742A>C
NM_000043.6:c.737A>C MANE Select	NP_000034.1:p.Lys246Thr
NM_001320619.2:c.*60A>C	NP_001307548.1:n.*60A>C
NM_152871.4:c.674A>C	NP_690610.1:p.Lys225Thr
NM_152872.4:c.*49A>C	NP_690611.1:n.*49A>C
NR_028033.4:n.644A>C
NR_028034.4:n.506A>C
NR_028035.4:n.569A>C
NR_028036.4:n.707A>C
NR_135313.2:n.624A>C
NR_135314.2:n.903A>C
NR_135315.2:n.656A>C