Canonical Allele Identifier: CA377510037

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774086A>C (hg19) ; chr10:g.89014329A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014329A>C , CM000672.2:g.89014329A>C	GRCh38
NC_000010.10:g.90774086A>C , CM000672.1:g.90774086A>C	GRCh37
NC_000010.9:g.90764066A>C	NCBI36
NG_009089.2:g.28799A>C , LRG_134:g.28799A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1196A>C
ENST00000355740.8:c.*210A>C	ENSP00000347979.3:n.*210A>C
ENST00000357339.7:c.824A>C	ENSP00000349896.2:p.Lys275Thr
ENST00000371857.8:n.2432A>C
ENST00000460510.6:c.170A>C	ENSP00000512812.1:p.Lys57Thr
ENST00000466081.6:n.2536A>C
ENST00000477270.6:c.932A>C	ENSP00000512813.1:p.Lys311Thr
ENST00000479522.6:c.*316A>C	ENSP00000424113.1:n.*316A>C
ENST00000484444.6:c.*328A>C	ENSP00000420975.1:n.*328A>C
ENST00000488877.6:c.778A>C	ENSP00000425159.1:n.778A>C
ENST00000492756.7:c.*316A>C	ENSP00000422453.1:n.*316A>C
ENST00000494799.6:c.170A>C	ENSP00000512834.1:p.Lys57Thr
ENST00000562983.3:c.170A>C	ENSP00000512845.1:p.Lys57Thr
ENST00000612663.6:c.*289A>C	ENSP00000477997.3:n.*289A>C
ENST00000640140.2:n.1032A>C
ENST00000640250.2:n.386A>C
ENST00000640681.2:n.991A>C
ENST00000696723.1:n.4520A>C
ENST00000696741.1:n.2525A>C
ENST00000696742.1:n.2252A>C
ENST00000696743.1:n.3655A>C
ENST00000696744.1:n.926A>C
ENST00000696767.1:n.1221A>C
ENST00000696768.1:c.*210A>C	ENSP00000512859.1:n.*210A>C
ENST00000696769.1:n.2576A>C
ENST00000696771.1:c.170A>C	ENSP00000512860.1:p.Lys57Thr
ENST00000696772.1:n.2490A>C
ENST00000696773.1:n.2229A>C
ENST00000696774.1:n.5997A>C
ENST00000696776.1:c.980A>C	ENSP00000512861.1:p.Lys327Thr
ENST00000696777.1:n.2295A>C
ENST00000696778.1:n.1323A>C
ENST00000696779.1:c.494A>C	ENSP00000512862.1:p.Lys165Thr
ENST00000696780.1:c.917A>C	ENSP00000512863.1:p.Lys306Thr
ENST00000696781.1:c.632A>C	ENSP00000512864.1:p.Lys211Thr
ENST00000696782.1:c.*289A>C	ENSP00000512865.1:n.*289A>C
ENST00000696783.1:n.2755A>C
ENST00000696992.1:n.2004A>C
ENST00000696995.1:n.4416A>C
ENST00000696996.1:n.2329A>C
ENST00000696997.1:c.*517A>C	ENSP00000513028.1:n.*517A>C
ENST00000696998.1:n.2141A>C
ENST00000696999.1:c.170A>C	ENSP00000513029.1:p.Lys57Thr
ENST00000697036.1:c.*303A>C	ENSP00000513060.1:n.*303A>C
ENST00000697037.1:n.922A>C
ENST00000697093.1:n.3123A>C
ENST00000697094.1:n.3470A>C
ENST00000697095.1:c.*2088A>C	ENSP00000513104.1:n.*2088A>C
ENST00000697096.1:n.2020A>C
ENST00000697097.1:c.170A>C	ENSP00000513105.1:p.Lys57Thr
ENST00000562983.2:n.1073A>C
ENST00000690268.1:c.968A>C	ENSP00000509810.1:p.Lys323Thr
ENST00000355740.7:c.*213A>C	ENSP00000347979.3:n.*213A>C
ENST00000612663.5:c.*289A>C	ENSP00000477997.3:n.*289A>C
ENST00000640140.1:n.1059A>C
ENST00000640250.1:n.386A>C
ENST00000640681.1:n.1008A>C
ENST00000652046.1:c.887A>C MANE Select	ENSP00000498466.1:p.Lys296Thr
ENST00000352159.8:c.*204A>C	ENSP00000345601.4:n.*204A>C
ENST00000355279.2:c.862A>C	ENSP00000347426.2:n.862A>C
ENST00000355740.6:c.887A>C	ENSP00000347979.2:p.Lys296Thr
ENST00000357339.6:c.824A>C	ENSP00000349896.2:p.Lys275Thr
ENST00000479522.5:c.*316A>C	ENSP00000424113.1:n.*316A>C
ENST00000484444.5:c.*328A>C	ENSP00000420975.1:n.*328A>C
ENST00000488877.5:c.*328A>C	ENSP00000425159.1:n.*328A>C
ENST00000492756.5:c.715A>C	ENSP00000422453.1:n.715A>C
ENST00000494410.5:c.*245A>C	ENSP00000423755.1:n.*245A>C
ENST00000612663.4:c.*234A>C	ENSP00000477997.2:n.*234A>C
NM_000043.4:c.887A>C , LRG_134t1:c.887A>C	NP_000034.1:p.Lys296Thr
NM_152871.2:c.824A>C	NP_690610.1:p.Lys275Thr
NM_152872.2:c.*199A>C	NP_690611.1:n.*199A>C
NR_028033.2:n.1061A>C
NR_028034.2:n.923A>C
NR_028035.2:n.986A>C
NR_028036.2:n.1124A>C
XM_006717819.2:c.968A>C	XP_006717882.1:p.Lys323Thr
XM_011539764.1:c.1049A>C	XP_011538066.1:p.Lys350Thr
XM_011539765.1:c.986A>C	XP_011538067.1:p.Lys329Thr
XM_011539766.1:c.968A>C	XP_011538068.1:p.Lys323Thr
XM_011539767.1:c.932A>C	XP_011538069.1:p.Lys311Thr
XR_945732.1:n.955A>C
XR_945733.1:n.892A>C
NM_000043.5:c.887A>C	NP_000034.1:p.Lys296Thr
NM_001320619.1:c.*210A>C	NP_001307548.1:n.*210A>C
NM_152871.3:c.824A>C	NP_690610.1:p.Lys275Thr
NM_152872.3:c.*199A>C	NP_690611.1:n.*199A>C
NR_028033.3:n.1033A>C
NR_028034.3:n.895A>C
NR_028035.3:n.958A>C
NR_028036.3:n.1096A>C
NR_135313.1:n.1013A>C
NR_135314.1:n.1196A>C
NR_135315.1:n.949A>C
XM_006717819.3:c.968A>C	XP_006717882.1:p.Lys323Thr
XM_011539764.2:c.1049A>C	XP_011538066.1:p.Lys350Thr
XM_011539765.2:c.986A>C	XP_011538067.1:p.Lys329Thr
XM_011539766.2:c.968A>C	XP_011538068.1:p.Lys323Thr
XM_011539767.3:c.932A>C	XP_011538069.1:p.Lys311Thr
XR_945732.3:n.955A>C
XR_945733.2:n.892A>C
NM_000043.6:c.887A>C MANE Select	NP_000034.1:p.Lys296Thr
NM_001320619.2:c.*210A>C	NP_001307548.1:n.*210A>C
NM_152871.4:c.824A>C	NP_690610.1:p.Lys275Thr
NM_152872.4:c.*199A>C	NP_690611.1:n.*199A>C
NR_028033.4:n.794A>C
NR_028034.4:n.656A>C
NR_028035.4:n.719A>C
NR_028036.4:n.857A>C
NR_135313.2:n.774A>C
NR_135314.2:n.1053A>C
NR_135315.2:n.806A>C