Canonical Allele Identifier: CA470974906

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774069G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014312G>C , CM000672.2:g.89014312G>C	GRCh38
NC_000010.10:g.90774069G>C , CM000672.1:g.90774069G>C	GRCh37
NC_000010.9:g.90764049G>C	NCBI36
NG_009089.2:g.28782G>C , LRG_134:g.28782G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1179G>C
ENST00000355740.8:c.*193G>C	ENSP00000347979.3:n.*193G>C
ENST00000357339.7:c.807G>C	ENSP00000349896.2:p.Ala269=
ENST00000371857.8:n.2415G>C
ENST00000460510.6:c.153G>C	ENSP00000512812.1:p.Ala51=
ENST00000466081.6:n.2519G>C
ENST00000477270.6:c.915G>C	ENSP00000512813.1:p.Ala305=
ENST00000479522.6:c.*299G>C	ENSP00000424113.1:n.*299G>C
ENST00000484444.6:c.*311G>C	ENSP00000420975.1:n.*311G>C
ENST00000488877.6:c.761G>C	ENSP00000425159.1:n.761G>C
ENST00000492756.7:c.*299G>C	ENSP00000422453.1:n.*299G>C
ENST00000494799.6:c.153G>C	ENSP00000512834.1:p.Ala51=
ENST00000562983.3:c.153G>C	ENSP00000512845.1:p.Ala51=
ENST00000612663.6:c.*272G>C	ENSP00000477997.3:n.*272G>C
ENST00000640140.2:n.1015G>C
ENST00000640250.2:n.369G>C
ENST00000640681.2:n.974G>C
ENST00000696723.1:n.4503G>C
ENST00000696741.1:n.2508G>C
ENST00000696742.1:n.2235G>C
ENST00000696743.1:n.3638G>C
ENST00000696744.1:n.909G>C
ENST00000696767.1:n.1204G>C
ENST00000696768.1:c.*193G>C	ENSP00000512859.1:n.*193G>C
ENST00000696769.1:n.2559G>C
ENST00000696771.1:c.153G>C	ENSP00000512860.1:p.Ala51=
ENST00000696772.1:n.2473G>C
ENST00000696773.1:n.2212G>C
ENST00000696774.1:n.5980G>C
ENST00000696776.1:c.963G>C	ENSP00000512861.1:p.Ala321=
ENST00000696777.1:n.2278G>C
ENST00000696778.1:n.1306G>C
ENST00000696779.1:c.477G>C	ENSP00000512862.1:p.Ala159=
ENST00000696780.1:c.900G>C	ENSP00000512863.1:p.Ala300=
ENST00000696781.1:c.615G>C	ENSP00000512864.1:p.Ala205=
ENST00000696782.1:c.*272G>C	ENSP00000512865.1:n.*272G>C
ENST00000696783.1:n.2738G>C
ENST00000696992.1:n.1987G>C
ENST00000696995.1:n.4399G>C
ENST00000696996.1:n.2312G>C
ENST00000696997.1:c.*500G>C	ENSP00000513028.1:n.*500G>C
ENST00000696998.1:n.2124G>C
ENST00000696999.1:c.153G>C	ENSP00000513029.1:p.Ala51=
ENST00000697036.1:c.*286G>C	ENSP00000513060.1:n.*286G>C
ENST00000697037.1:n.905G>C
ENST00000697093.1:n.3106G>C
ENST00000697094.1:n.3453G>C
ENST00000697095.1:c.*2071G>C	ENSP00000513104.1:n.*2071G>C
ENST00000697096.1:n.2003G>C
ENST00000697097.1:c.153G>C	ENSP00000513105.1:p.Ala51=
ENST00000562983.2:n.1056G>C
ENST00000690268.1:c.951G>C	ENSP00000509810.1:p.Ala317=
ENST00000355740.7:c.*196G>C	ENSP00000347979.3:n.*196G>C
ENST00000612663.5:c.*272G>C	ENSP00000477997.3:n.*272G>C
ENST00000640140.1:n.1042G>C
ENST00000640250.1:n.369G>C
ENST00000640681.1:n.991G>C
ENST00000652046.1:c.870G>C MANE Select	ENSP00000498466.1:p.Ala290=
ENST00000352159.8:c.*187G>C	ENSP00000345601.4:n.*187G>C
ENST00000355279.2:c.845G>C	ENSP00000347426.2:n.845G>C
ENST00000355740.6:c.870G>C	ENSP00000347979.2:p.Ala290=
ENST00000357339.6:c.807G>C	ENSP00000349896.2:p.Ala269=
ENST00000479522.5:c.*299G>C	ENSP00000424113.1:n.*299G>C
ENST00000484444.5:c.*311G>C	ENSP00000420975.1:n.*311G>C
ENST00000488877.5:c.*311G>C	ENSP00000425159.1:n.*311G>C
ENST00000492756.5:c.698G>C	ENSP00000422453.1:n.698G>C
ENST00000494410.5:c.*228G>C	ENSP00000423755.1:n.*228G>C
ENST00000612663.4:c.*217G>C	ENSP00000477997.2:n.*217G>C
NM_000043.4:c.870G>C , LRG_134t1:c.870G>C	NP_000034.1:p.Ala290=
NM_152871.2:c.807G>C	NP_690610.1:p.Ala269=
NM_152872.2:c.*182G>C	NP_690611.1:n.*182G>C
NR_028033.2:n.1044G>C
NR_028034.2:n.906G>C
NR_028035.2:n.969G>C
NR_028036.2:n.1107G>C
XM_006717819.2:c.951G>C	XP_006717882.1:p.Ala317=
XM_011539764.1:c.1032G>C	XP_011538066.1:p.Ala344=
XM_011539765.1:c.969G>C	XP_011538067.1:p.Ala323=
XM_011539766.1:c.951G>C	XP_011538068.1:p.Ala317=
XM_011539767.1:c.915G>C	XP_011538069.1:p.Ala305=
XR_945732.1:n.938G>C
XR_945733.1:n.875G>C
NM_000043.5:c.870G>C	NP_000034.1:p.Ala290=
NM_001320619.1:c.*193G>C	NP_001307548.1:n.*193G>C
NM_152871.3:c.807G>C	NP_690610.1:p.Ala269=
NM_152872.3:c.*182G>C	NP_690611.1:n.*182G>C
NR_028033.3:n.1016G>C
NR_028034.3:n.878G>C
NR_028035.3:n.941G>C
NR_028036.3:n.1079G>C
NR_135313.1:n.996G>C
NR_135314.1:n.1179G>C
NR_135315.1:n.932G>C
XM_006717819.3:c.951G>C	XP_006717882.1:p.Ala317=
XM_011539764.2:c.1032G>C	XP_011538066.1:p.Ala344=
XM_011539765.2:c.969G>C	XP_011538067.1:p.Ala323=
XM_011539766.2:c.951G>C	XP_011538068.1:p.Ala317=
XM_011539767.3:c.915G>C	XP_011538069.1:p.Ala305=
XR_945732.3:n.938G>C
XR_945733.2:n.875G>C
NM_000043.6:c.870G>C MANE Select	NP_000034.1:p.Ala290=
NM_001320619.2:c.*193G>C	NP_001307548.1:n.*193G>C
NM_152871.4:c.807G>C	NP_690610.1:p.Ala269=
NM_152872.4:c.*182G>C	NP_690611.1:n.*182G>C
NR_028033.4:n.777G>C
NR_028034.4:n.639G>C
NR_028035.4:n.702G>C
NR_028036.4:n.840G>C
NR_135313.2:n.757G>C
NR_135314.2:n.1036G>C
NR_135315.2:n.789G>C