Canonical Allele Identifier: CA377509603

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773906T>C (hg19) ; chr10:g.89014149T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014149T>C , CM000672.2:g.89014149T>C	GRCh38
NC_000010.10:g.90773906T>C , CM000672.1:g.90773906T>C	GRCh37
NC_000010.9:g.90763886T>C	NCBI36
NG_009089.2:g.28619T>C , LRG_134:g.28619T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1016T>C
ENST00000355740.8:c.*30T>C	ENSP00000347979.3:n.*30T>C
ENST00000357339.7:c.644T>C	ENSP00000349896.2:p.Ile215Thr
ENST00000371857.8:n.2252T>C
ENST00000460510.6:c.-11T>C	ENSP00000512812.1:n.-11T>C
ENST00000466081.6:n.2356T>C
ENST00000477270.6:c.752T>C	ENSP00000512813.1:p.Ile251Thr
ENST00000479522.6:c.*136T>C	ENSP00000424113.1:n.*136T>C
ENST00000484444.6:c.*148T>C	ENSP00000420975.1:n.*148T>C
ENST00000488877.6:c.598T>C	ENSP00000425159.1:n.598T>C
ENST00000492756.7:c.*136T>C	ENSP00000422453.1:n.*136T>C
ENST00000494799.6:c.-11T>C	ENSP00000512834.1:n.-11T>C
ENST00000562983.3:c.-11T>C	ENSP00000512845.1:n.-11T>C
ENST00000612663.6:c.*109T>C	ENSP00000477997.3:n.*109T>C
ENST00000640140.2:n.852T>C
ENST00000640250.2:n.206T>C
ENST00000640681.2:n.811T>C
ENST00000696723.1:n.4340T>C
ENST00000696741.1:n.2345T>C
ENST00000696742.1:n.2072T>C
ENST00000696743.1:n.3475T>C
ENST00000696744.1:n.746T>C
ENST00000696767.1:n.1041T>C
ENST00000696768.1:c.*30T>C	ENSP00000512859.1:n.*30T>C
ENST00000696769.1:n.2396T>C
ENST00000696771.1:c.-11T>C	ENSP00000512860.1:n.-11T>C
ENST00000696772.1:n.2310T>C
ENST00000696773.1:n.2049T>C
ENST00000696774.1:n.5817T>C
ENST00000696776.1:c.800T>C	ENSP00000512861.1:p.Ile267Thr
ENST00000696777.1:n.2115T>C
ENST00000696778.1:n.1143T>C
ENST00000696779.1:c.314T>C	ENSP00000512862.1:p.Ile105Thr
ENST00000696780.1:c.737T>C	ENSP00000512863.1:p.Ile246Thr
ENST00000696781.1:c.452T>C	ENSP00000512864.1:p.Ile151Thr
ENST00000696782.1:c.*109T>C	ENSP00000512865.1:n.*109T>C
ENST00000696783.1:n.2575T>C
ENST00000696992.1:n.1824T>C
ENST00000696995.1:n.4236T>C
ENST00000696996.1:n.2149T>C
ENST00000696997.1:c.*337T>C	ENSP00000513028.1:n.*337T>C
ENST00000696998.1:n.1961T>C
ENST00000696999.1:c.-11T>C	ENSP00000513029.1:n.-11T>C
ENST00000697035.1:c.*40T>C	ENSP00000513059.1:n.*40T>C
ENST00000697036.1:c.*123T>C	ENSP00000513060.1:n.*123T>C
ENST00000697037.1:n.742T>C
ENST00000697093.1:n.2943T>C
ENST00000697094.1:n.3290T>C
ENST00000697095.1:c.*1908T>C	ENSP00000513104.1:n.*1908T>C
ENST00000697096.1:n.1840T>C
ENST00000697097.1:c.-11T>C	ENSP00000513105.1:n.-11T>C
ENST00000562983.2:n.893T>C
ENST00000690268.1:c.788T>C	ENSP00000509810.1:p.Ile263Thr
ENST00000355740.7:c.*33T>C	ENSP00000347979.3:n.*33T>C
ENST00000612663.5:c.*109T>C	ENSP00000477997.3:n.*109T>C
ENST00000640140.1:n.879T>C
ENST00000640250.1:n.206T>C
ENST00000640681.1:n.828T>C
ENST00000652046.1:c.707T>C MANE Select	ENSP00000498466.1:p.Ile236Thr
ENST00000313771.9:n.1016T>C
ENST00000352159.8:c.*24T>C	ENSP00000345601.4:n.*24T>C
ENST00000355279.2:c.682T>C	ENSP00000347426.2:n.682T>C
ENST00000355740.6:c.707T>C	ENSP00000347979.2:p.Ile236Thr
ENST00000357339.6:c.644T>C	ENSP00000349896.2:p.Ile215Thr
ENST00000479522.5:c.*136T>C	ENSP00000424113.1:n.*136T>C
ENST00000484444.5:c.*148T>C	ENSP00000420975.1:n.*148T>C
ENST00000488877.5:c.*148T>C	ENSP00000425159.1:n.*148T>C
ENST00000492756.5:c.535T>C	ENSP00000422453.1:n.535T>C
ENST00000494410.5:c.*65T>C	ENSP00000423755.1:n.*65T>C
ENST00000494799.5:n.614T>C
ENST00000612663.4:c.*54T>C	ENSP00000477997.2:n.*54T>C
ENST00000615406.4:c.707T>C	ENSP00000484575.1:p.Ile236Thr
ENST00000626542.2:c.705T>C	ENSP00000485876.1:p.Tyr235=
NM_000043.4:c.707T>C , LRG_134t1:c.707T>C	NP_000034.1:p.Ile236Thr
NM_152871.2:c.644T>C	NP_690610.1:p.Ile215Thr
NM_152872.2:c.*19T>C	NP_690611.1:n.*19T>C
NR_028033.2:n.881T>C
NR_028034.2:n.743T>C
NR_028035.2:n.806T>C
NR_028036.2:n.944T>C
XM_006717819.2:c.788T>C	XP_006717882.1:p.Ile263Thr
XM_011539764.1:c.869T>C	XP_011538066.1:p.Ile290Thr
XM_011539765.1:c.806T>C	XP_011538067.1:p.Ile269Thr
XM_011539766.1:c.788T>C	XP_011538068.1:p.Ile263Thr
XM_011539767.1:c.752T>C	XP_011538069.1:p.Ile251Thr
XR_945732.1:n.775T>C
XR_945733.1:n.712T>C
NM_000043.5:c.707T>C	NP_000034.1:p.Ile236Thr
NM_001320619.1:c.*30T>C	NP_001307548.1:n.*30T>C
NM_152871.3:c.644T>C	NP_690610.1:p.Ile215Thr
NM_152872.3:c.*19T>C	NP_690611.1:n.*19T>C
NR_028033.3:n.853T>C
NR_028034.3:n.715T>C
NR_028035.3:n.778T>C
NR_028036.3:n.916T>C
NR_135313.1:n.833T>C
NR_135314.1:n.1016T>C
NR_135315.1:n.769T>C
XM_006717819.3:c.788T>C	XP_006717882.1:p.Ile263Thr
XM_011539764.2:c.869T>C	XP_011538066.1:p.Ile290Thr
XM_011539765.2:c.806T>C	XP_011538067.1:p.Ile269Thr
XM_011539766.2:c.788T>C	XP_011538068.1:p.Ile263Thr
XM_011539767.3:c.752T>C	XP_011538069.1:p.Ile251Thr
XR_945732.3:n.775T>C
XR_945733.2:n.712T>C
NM_000043.6:c.707T>C MANE Select	NP_000034.1:p.Ile236Thr
NM_001320619.2:c.*30T>C	NP_001307548.1:n.*30T>C
NM_152871.4:c.644T>C	NP_690610.1:p.Ile215Thr
NM_152872.4:c.*19T>C	NP_690611.1:n.*19T>C
NR_028033.4:n.614T>C
NR_028034.4:n.476T>C
NR_028035.4:n.539T>C
NR_028036.4:n.677T>C
NR_135313.2:n.594T>C
NR_135314.2:n.873T>C
NR_135315.2:n.626T>C