Canonical Allele Identifier: CA377509538

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773881G>C (hg19) ; chr10:g.89014124G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014124G>C , CM000672.2:g.89014124G>C	GRCh38
NC_000010.10:g.90773881G>C , CM000672.1:g.90773881G>C	GRCh37
NC_000010.9:g.90763861G>C	NCBI36
NG_009089.2:g.28594G>C , LRG_134:g.28594G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.991G>C
ENST00000355740.8:c.*5G>C	ENSP00000347979.3:n.*5G>C
ENST00000357339.7:c.619G>C	ENSP00000349896.2:p.Asp207His
ENST00000371857.8:n.2227G>C
ENST00000460510.6:c.-36G>C	ENSP00000512812.1:n.-36G>C
ENST00000466081.6:n.2331G>C
ENST00000477270.6:c.727G>C	ENSP00000512813.1:p.Asp243His
ENST00000479522.6:c.*111G>C	ENSP00000424113.1:n.*111G>C
ENST00000484444.6:c.*123G>C	ENSP00000420975.1:n.*123G>C
ENST00000488877.6:c.573G>C	ENSP00000425159.1:n.573G>C
ENST00000492756.7:c.*111G>C	ENSP00000422453.1:n.*111G>C
ENST00000494799.6:c.-36G>C	ENSP00000512834.1:n.-36G>C
ENST00000562983.3:c.-36G>C	ENSP00000512845.1:n.-36G>C
ENST00000612663.6:c.*84G>C	ENSP00000477997.3:n.*84G>C
ENST00000640140.2:n.827G>C
ENST00000640250.2:n.181G>C
ENST00000640681.2:n.786G>C
ENST00000696723.1:n.4315G>C
ENST00000696741.1:n.2320G>C
ENST00000696742.1:n.2047G>C
ENST00000696743.1:n.3450G>C
ENST00000696744.1:n.721G>C
ENST00000696767.1:n.1016G>C
ENST00000696768.1:c.*5G>C	ENSP00000512859.1:n.*5G>C
ENST00000696769.1:n.2371G>C
ENST00000696771.1:c.-36G>C	ENSP00000512860.1:n.-36G>C
ENST00000696772.1:n.2285G>C
ENST00000696773.1:n.2024G>C
ENST00000696774.1:n.5792G>C
ENST00000696776.1:c.775G>C	ENSP00000512861.1:p.Asp259His
ENST00000696777.1:n.2090G>C
ENST00000696778.1:n.1118G>C
ENST00000696779.1:c.289G>C	ENSP00000512862.1:p.Asp97His
ENST00000696780.1:c.712G>C	ENSP00000512863.1:p.Asp238His
ENST00000696781.1:c.427G>C	ENSP00000512864.1:p.Asp143His
ENST00000696782.1:c.*84G>C	ENSP00000512865.1:n.*84G>C
ENST00000696783.1:n.2550G>C
ENST00000696992.1:n.1799G>C
ENST00000696995.1:n.4211G>C
ENST00000696996.1:n.2124G>C
ENST00000696997.1:c.*312G>C	ENSP00000513028.1:n.*312G>C
ENST00000696998.1:n.1936G>C
ENST00000696999.1:c.-36G>C	ENSP00000513029.1:n.-36G>C
ENST00000697035.1:c.*15G>C	ENSP00000513059.1:n.*15G>C
ENST00000697036.1:c.*98G>C	ENSP00000513060.1:n.*98G>C
ENST00000697037.1:n.717G>C
ENST00000697093.1:n.2918G>C
ENST00000697094.1:n.3265G>C
ENST00000697095.1:c.*1883G>C	ENSP00000513104.1:n.*1883G>C
ENST00000697096.1:n.1815G>C
ENST00000697097.1:c.-36G>C	ENSP00000513105.1:n.-36G>C
ENST00000562983.2:n.868G>C
ENST00000690268.1:c.763G>C	ENSP00000509810.1:p.Asp255His
ENST00000355740.7:c.*8G>C	ENSP00000347979.3:n.*8G>C
ENST00000612663.5:c.*84G>C	ENSP00000477997.3:n.*84G>C
ENST00000640140.1:n.854G>C
ENST00000640250.1:n.181G>C
ENST00000640681.1:n.803G>C
ENST00000652046.1:c.682G>C MANE Select	ENSP00000498466.1:p.Asp228His
ENST00000313771.9:n.991G>C
ENST00000352159.8:c.701G>C	ENSP00000345601.4:p.Ter234Ser
ENST00000355279.2:c.657G>C	ENSP00000347426.2:p.Leu219Phe
ENST00000355740.6:c.682G>C	ENSP00000347979.2:p.Asp228His
ENST00000357339.6:c.619G>C	ENSP00000349896.2:p.Asp207His
ENST00000479522.5:c.*111G>C	ENSP00000424113.1:n.*111G>C
ENST00000484444.5:c.*123G>C	ENSP00000420975.1:n.*123G>C
ENST00000488877.5:c.*123G>C	ENSP00000425159.1:n.*123G>C
ENST00000492756.5:c.510G>C	ENSP00000422453.1:n.510G>C
ENST00000494410.5:c.*40G>C	ENSP00000423755.1:n.*40G>C
ENST00000494799.5:n.589G>C
ENST00000612663.4:c.*29G>C	ENSP00000477997.2:n.*29G>C
ENST00000615406.4:c.682G>C	ENSP00000484575.1:p.Asp228His
ENST00000626542.2:c.682G>C	ENSP00000485876.1:p.Asp228His
NM_000043.4:c.682G>C , LRG_134t1:c.682G>C	NP_000034.1:p.Asp228His
NM_152871.2:c.619G>C	NP_690610.1:p.Asp207His
NM_152872.2:c.657G>C	NP_690611.1:p.Leu219Phe
NR_028033.2:n.856G>C
NR_028034.2:n.718G>C
NR_028035.2:n.781G>C
NR_028036.2:n.919G>C
XM_006717819.2:c.763G>C	XP_006717882.1:p.Asp255His
XM_011539764.1:c.844G>C	XP_011538066.1:p.Asp282His
XM_011539765.1:c.781G>C	XP_011538067.1:p.Asp261His
XM_011539766.1:c.763G>C	XP_011538068.1:p.Asp255His
XM_011539767.1:c.727G>C	XP_011538069.1:p.Asp243His
XR_945732.1:n.750G>C
XR_945733.1:n.687G>C
NM_000043.5:c.682G>C	NP_000034.1:p.Asp228His
NM_001320619.1:c.*5G>C	NP_001307548.1:n.*5G>C
NM_152871.3:c.619G>C	NP_690610.1:p.Asp207His
NM_152872.3:c.657G>C	NP_690611.1:p.Leu219Phe
NR_028033.3:n.828G>C
NR_028034.3:n.690G>C
NR_028035.3:n.753G>C
NR_028036.3:n.891G>C
NR_135313.1:n.808G>C
NR_135314.1:n.991G>C
NR_135315.1:n.744G>C
XM_006717819.3:c.763G>C	XP_006717882.1:p.Asp255His
XM_011539764.2:c.844G>C	XP_011538066.1:p.Asp282His
XM_011539765.2:c.781G>C	XP_011538067.1:p.Asp261His
XM_011539766.2:c.763G>C	XP_011538068.1:p.Asp255His
XM_011539767.3:c.727G>C	XP_011538069.1:p.Asp243His
XR_945732.3:n.750G>C
XR_945733.2:n.687G>C
NM_000043.6:c.682G>C MANE Select	NP_000034.1:p.Asp228His
NM_001320619.2:c.*5G>C	NP_001307548.1:n.*5G>C
NM_152871.4:c.619G>C	NP_690610.1:p.Asp207His
NM_152872.4:c.657G>C	NP_690611.1:p.Leu219Phe
NR_028033.4:n.589G>C
NR_028034.4:n.451G>C
NR_028035.4:n.514G>C
NR_028036.4:n.652G>C
NR_135313.2:n.569G>C
NR_135314.2:n.848G>C
NR_135315.2:n.601G>C