Canonical Allele Identifier: CA470974881

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774054T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014297T>C , CM000672.2:g.89014297T>C	GRCh38
NC_000010.10:g.90774054T>C , CM000672.1:g.90774054T>C	GRCh37
NC_000010.9:g.90764034T>C	NCBI36
NG_009089.2:g.28767T>C , LRG_134:g.28767T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1164T>C
ENST00000355740.8:c.*178T>C	ENSP00000347979.3:n.*178T>C
ENST00000357339.7:c.792T>C	ENSP00000349896.2:p.His264=
ENST00000371857.8:n.2400T>C
ENST00000460510.6:c.138T>C	ENSP00000512812.1:p.His46=
ENST00000466081.6:n.2504T>C
ENST00000477270.6:c.900T>C	ENSP00000512813.1:p.His300=
ENST00000479522.6:c.*284T>C	ENSP00000424113.1:n.*284T>C
ENST00000484444.6:c.*296T>C	ENSP00000420975.1:n.*296T>C
ENST00000488877.6:c.746T>C	ENSP00000425159.1:n.746T>C
ENST00000492756.7:c.*284T>C	ENSP00000422453.1:n.*284T>C
ENST00000494799.6:c.138T>C	ENSP00000512834.1:p.His46=
ENST00000562983.3:c.138T>C	ENSP00000512845.1:p.His46=
ENST00000612663.6:c.*257T>C	ENSP00000477997.3:n.*257T>C
ENST00000640140.2:n.1000T>C
ENST00000640250.2:n.354T>C
ENST00000640681.2:n.959T>C
ENST00000696723.1:n.4488T>C
ENST00000696741.1:n.2493T>C
ENST00000696742.1:n.2220T>C
ENST00000696743.1:n.3623T>C
ENST00000696744.1:n.894T>C
ENST00000696767.1:n.1189T>C
ENST00000696768.1:c.*178T>C	ENSP00000512859.1:n.*178T>C
ENST00000696769.1:n.2544T>C
ENST00000696771.1:c.138T>C	ENSP00000512860.1:p.His46=
ENST00000696772.1:n.2458T>C
ENST00000696773.1:n.2197T>C
ENST00000696774.1:n.5965T>C
ENST00000696776.1:c.948T>C	ENSP00000512861.1:p.His316=
ENST00000696777.1:n.2263T>C
ENST00000696778.1:n.1291T>C
ENST00000696779.1:c.462T>C	ENSP00000512862.1:p.His154=
ENST00000696780.1:c.885T>C	ENSP00000512863.1:p.His295=
ENST00000696781.1:c.600T>C	ENSP00000512864.1:p.His200=
ENST00000696782.1:c.*257T>C	ENSP00000512865.1:n.*257T>C
ENST00000696783.1:n.2723T>C
ENST00000696992.1:n.1972T>C
ENST00000696995.1:n.4384T>C
ENST00000696996.1:n.2297T>C
ENST00000696997.1:c.*485T>C	ENSP00000513028.1:n.*485T>C
ENST00000696998.1:n.2109T>C
ENST00000696999.1:c.138T>C	ENSP00000513029.1:p.His46=
ENST00000697035.1:c.*188T>C	ENSP00000513059.1:n.*188T>C
ENST00000697036.1:c.*271T>C	ENSP00000513060.1:n.*271T>C
ENST00000697037.1:n.890T>C
ENST00000697093.1:n.3091T>C
ENST00000697094.1:n.3438T>C
ENST00000697095.1:c.*2056T>C	ENSP00000513104.1:n.*2056T>C
ENST00000697096.1:n.1988T>C
ENST00000697097.1:c.138T>C	ENSP00000513105.1:p.His46=
ENST00000562983.2:n.1041T>C
ENST00000690268.1:c.936T>C	ENSP00000509810.1:p.His312=
ENST00000355740.7:c.*181T>C	ENSP00000347979.3:n.*181T>C
ENST00000612663.5:c.*257T>C	ENSP00000477997.3:n.*257T>C
ENST00000640140.1:n.1027T>C
ENST00000640250.1:n.354T>C
ENST00000640681.1:n.976T>C
ENST00000652046.1:c.855T>C MANE Select	ENSP00000498466.1:p.His285=
ENST00000352159.8:c.*172T>C	ENSP00000345601.4:n.*172T>C
ENST00000355279.2:c.830T>C	ENSP00000347426.2:n.830T>C
ENST00000355740.6:c.855T>C	ENSP00000347979.2:p.His285=
ENST00000357339.6:c.792T>C	ENSP00000349896.2:p.His264=
ENST00000479522.5:c.*284T>C	ENSP00000424113.1:n.*284T>C
ENST00000484444.5:c.*296T>C	ENSP00000420975.1:n.*296T>C
ENST00000488877.5:c.*296T>C	ENSP00000425159.1:n.*296T>C
ENST00000492756.5:c.683T>C	ENSP00000422453.1:n.683T>C
ENST00000494410.5:c.*213T>C	ENSP00000423755.1:n.*213T>C
ENST00000612663.4:c.*202T>C	ENSP00000477997.2:n.*202T>C
NM_000043.4:c.855T>C , LRG_134t1:c.855T>C	NP_000034.1:p.His285=
NM_152871.2:c.792T>C	NP_690610.1:p.His264=
NM_152872.2:c.*167T>C	NP_690611.1:n.*167T>C
NR_028033.2:n.1029T>C
NR_028034.2:n.891T>C
NR_028035.2:n.954T>C
NR_028036.2:n.1092T>C
XM_006717819.2:c.936T>C	XP_006717882.1:p.His312=
XM_011539764.1:c.1017T>C	XP_011538066.1:p.His339=
XM_011539765.1:c.954T>C	XP_011538067.1:p.His318=
XM_011539766.1:c.936T>C	XP_011538068.1:p.His312=
XM_011539767.1:c.900T>C	XP_011538069.1:p.His300=
XR_945732.1:n.923T>C
XR_945733.1:n.860T>C
NM_000043.5:c.855T>C	NP_000034.1:p.His285=
NM_001320619.1:c.*178T>C	NP_001307548.1:n.*178T>C
NM_152871.3:c.792T>C	NP_690610.1:p.His264=
NM_152872.3:c.*167T>C	NP_690611.1:n.*167T>C
NR_028033.3:n.1001T>C
NR_028034.3:n.863T>C
NR_028035.3:n.926T>C
NR_028036.3:n.1064T>C
NR_135313.1:n.981T>C
NR_135314.1:n.1164T>C
NR_135315.1:n.917T>C
XM_006717819.3:c.936T>C	XP_006717882.1:p.His312=
XM_011539764.2:c.1017T>C	XP_011538066.1:p.His339=
XM_011539765.2:c.954T>C	XP_011538067.1:p.His318=
XM_011539766.2:c.936T>C	XP_011538068.1:p.His312=
XM_011539767.3:c.900T>C	XP_011538069.1:p.His300=
XR_945732.3:n.923T>C
XR_945733.2:n.860T>C
NM_000043.6:c.855T>C MANE Select	NP_000034.1:p.His285=
NM_001320619.2:c.*178T>C	NP_001307548.1:n.*178T>C
NM_152871.4:c.792T>C	NP_690610.1:p.His264=
NM_152872.4:c.*167T>C	NP_690611.1:n.*167T>C
NR_028033.4:n.762T>C
NR_028034.4:n.624T>C
NR_028035.4:n.687T>C
NR_028036.4:n.825T>C
NR_135313.2:n.742T>C
NR_135314.2:n.1021T>C
NR_135315.2:n.774T>C