Canonical Allele Identifier: CA470974939

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774117T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014360T>C , CM000672.2:g.89014360T>C	GRCh38
NC_000010.10:g.90774117T>C , CM000672.1:g.90774117T>C	GRCh37
NC_000010.9:g.90764097T>C	NCBI36
NG_009089.2:g.28830T>C , LRG_134:g.28830T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1227T>C
ENST00000355740.8:c.*241T>C	ENSP00000347979.3:n.*241T>C
ENST00000357339.7:c.855T>C	ENSP00000349896.2:p.Leu285=
ENST00000371857.8:n.2463T>C
ENST00000460510.6:c.201T>C	ENSP00000512812.1:p.Leu67=
ENST00000466081.6:n.2567T>C
ENST00000477270.6:c.963T>C	ENSP00000512813.1:p.Leu321=
ENST00000479522.6:c.*347T>C	ENSP00000424113.1:n.*347T>C
ENST00000484444.6:c.*359T>C	ENSP00000420975.1:n.*359T>C
ENST00000488877.6:c.809T>C	ENSP00000425159.1:n.809T>C
ENST00000492756.7:c.*347T>C	ENSP00000422453.1:n.*347T>C
ENST00000494799.6:c.201T>C	ENSP00000512834.1:p.Leu67=
ENST00000562983.3:c.201T>C	ENSP00000512845.1:p.Leu67=
ENST00000612663.6:c.*320T>C	ENSP00000477997.3:n.*320T>C
ENST00000640140.2:n.1063T>C
ENST00000640250.2:n.417T>C
ENST00000640681.2:n.1022T>C
ENST00000696723.1:n.4551T>C
ENST00000696741.1:n.2556T>C
ENST00000696742.1:n.2283T>C
ENST00000696743.1:n.3686T>C
ENST00000696744.1:n.957T>C
ENST00000696767.1:n.1252T>C
ENST00000696768.1:c.*241T>C	ENSP00000512859.1:n.*241T>C
ENST00000696769.1:n.2607T>C
ENST00000696771.1:c.201T>C	ENSP00000512860.1:p.Leu67=
ENST00000696772.1:n.2521T>C
ENST00000696773.1:n.2260T>C
ENST00000696774.1:n.6028T>C
ENST00000696776.1:c.1011T>C	ENSP00000512861.1:p.Leu337=
ENST00000696777.1:n.2326T>C
ENST00000696778.1:n.1354T>C
ENST00000696779.1:c.525T>C	ENSP00000512862.1:p.Leu175=
ENST00000696780.1:c.948T>C	ENSP00000512863.1:p.Leu316=
ENST00000696781.1:c.663T>C	ENSP00000512864.1:p.Leu221=
ENST00000696782.1:c.*320T>C	ENSP00000512865.1:n.*320T>C
ENST00000696783.1:n.2786T>C
ENST00000696992.1:n.2035T>C
ENST00000696995.1:n.4447T>C
ENST00000696996.1:n.2360T>C
ENST00000696997.1:c.*548T>C	ENSP00000513028.1:n.*548T>C
ENST00000696998.1:n.2172T>C
ENST00000696999.1:c.201T>C	ENSP00000513029.1:p.Leu67=
ENST00000697036.1:c.*334T>C	ENSP00000513060.1:n.*334T>C
ENST00000697037.1:n.953T>C
ENST00000697093.1:n.3154T>C
ENST00000697094.1:n.3501T>C
ENST00000697095.1:c.*2119T>C	ENSP00000513104.1:n.*2119T>C
ENST00000697096.1:n.2051T>C
ENST00000697097.1:c.201T>C	ENSP00000513105.1:p.Leu67=
ENST00000562983.2:n.1104T>C
ENST00000690268.1:c.999T>C	ENSP00000509810.1:p.Leu333=
ENST00000355740.7:c.*244T>C	ENSP00000347979.3:n.*244T>C
ENST00000612663.5:c.*320T>C	ENSP00000477997.3:n.*320T>C
ENST00000640140.1:n.1090T>C
ENST00000640250.1:n.417T>C
ENST00000640681.1:n.1039T>C
ENST00000652046.1:c.918T>C MANE Select	ENSP00000498466.1:p.Leu306=
ENST00000352159.8:c.*235T>C	ENSP00000345601.4:n.*235T>C
ENST00000355279.2:c.893T>C	ENSP00000347426.2:n.893T>C
ENST00000355740.6:c.918T>C	ENSP00000347979.2:p.Leu306=
ENST00000357339.6:c.855T>C	ENSP00000349896.2:p.Leu285=
ENST00000479522.5:c.*347T>C	ENSP00000424113.1:n.*347T>C
ENST00000484444.5:c.*359T>C	ENSP00000420975.1:n.*359T>C
ENST00000488877.5:c.*359T>C	ENSP00000425159.1:n.*359T>C
ENST00000492756.5:c.746T>C	ENSP00000422453.1:n.746T>C
ENST00000494410.5:c.*276T>C	ENSP00000423755.1:n.*276T>C
ENST00000612663.4:c.*265T>C	ENSP00000477997.2:n.*265T>C
NM_000043.4:c.918T>C , LRG_134t1:c.918T>C	NP_000034.1:p.Leu306=
NM_152871.2:c.855T>C	NP_690610.1:p.Leu285=
NM_152872.2:c.*230T>C	NP_690611.1:n.*230T>C
NR_028033.2:n.1092T>C
NR_028034.2:n.954T>C
NR_028035.2:n.1017T>C
NR_028036.2:n.1155T>C
XM_006717819.2:c.999T>C	XP_006717882.1:p.Leu333=
XM_011539764.1:c.1080T>C	XP_011538066.1:p.Leu360=
XM_011539765.1:c.1017T>C	XP_011538067.1:p.Leu339=
XM_011539766.1:c.999T>C	XP_011538068.1:p.Leu333=
XM_011539767.1:c.963T>C	XP_011538069.1:p.Leu321=
XR_945732.1:n.986T>C
XR_945733.1:n.923T>C
NM_000043.5:c.918T>C	NP_000034.1:p.Leu306=
NM_001320619.1:c.*241T>C	NP_001307548.1:n.*241T>C
NM_152871.3:c.855T>C	NP_690610.1:p.Leu285=
NM_152872.3:c.*230T>C	NP_690611.1:n.*230T>C
NR_028033.3:n.1064T>C
NR_028034.3:n.926T>C
NR_028035.3:n.989T>C
NR_028036.3:n.1127T>C
NR_135313.1:n.1044T>C
NR_135314.1:n.1227T>C
NR_135315.1:n.980T>C
XM_006717819.3:c.999T>C	XP_006717882.1:p.Leu333=
XM_011539764.2:c.1080T>C	XP_011538066.1:p.Leu360=
XM_011539765.2:c.1017T>C	XP_011538067.1:p.Leu339=
XM_011539766.2:c.999T>C	XP_011538068.1:p.Leu333=
XM_011539767.3:c.963T>C	XP_011538069.1:p.Leu321=
XR_945732.3:n.986T>C
XR_945733.2:n.923T>C
NM_000043.6:c.918T>C MANE Select	NP_000034.1:p.Leu306=
NM_001320619.2:c.*241T>C	NP_001307548.1:n.*241T>C
NM_152871.4:c.855T>C	NP_690610.1:p.Leu285=
NM_152872.4:c.*230T>C	NP_690611.1:n.*230T>C
NR_028033.4:n.825T>C
NR_028034.4:n.687T>C
NR_028035.4:n.750T>C
NR_028036.4:n.888T>C
NR_135313.2:n.805T>C
NR_135314.2:n.1084T>C
NR_135315.2:n.837T>C