Canonical Allele Identifier: CA470974923

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774090T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014333T>C , CM000672.2:g.89014333T>C	GRCh38
NC_000010.10:g.90774090T>C , CM000672.1:g.90774090T>C	GRCh37
NC_000010.9:g.90764070T>C	NCBI36
NG_009089.2:g.28803T>C , LRG_134:g.28803T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1200T>C
ENST00000355740.8:c.*214T>C	ENSP00000347979.3:n.*214T>C
ENST00000357339.7:c.828T>C	ENSP00000349896.2:p.Asp276=
ENST00000371857.8:n.2436T>C
ENST00000460510.6:c.174T>C	ENSP00000512812.1:p.Asp58=
ENST00000466081.6:n.2540T>C
ENST00000477270.6:c.936T>C	ENSP00000512813.1:p.Asp312=
ENST00000479522.6:c.*320T>C	ENSP00000424113.1:n.*320T>C
ENST00000484444.6:c.*332T>C	ENSP00000420975.1:n.*332T>C
ENST00000488877.6:c.782T>C	ENSP00000425159.1:n.782T>C
ENST00000492756.7:c.*320T>C	ENSP00000422453.1:n.*320T>C
ENST00000494799.6:c.174T>C	ENSP00000512834.1:p.Asp58=
ENST00000562983.3:c.174T>C	ENSP00000512845.1:p.Asp58=
ENST00000612663.6:c.*293T>C	ENSP00000477997.3:n.*293T>C
ENST00000640140.2:n.1036T>C
ENST00000640250.2:n.390T>C
ENST00000640681.2:n.995T>C
ENST00000696723.1:n.4524T>C
ENST00000696741.1:n.2529T>C
ENST00000696742.1:n.2256T>C
ENST00000696743.1:n.3659T>C
ENST00000696744.1:n.930T>C
ENST00000696767.1:n.1225T>C
ENST00000696768.1:c.*214T>C	ENSP00000512859.1:n.*214T>C
ENST00000696769.1:n.2580T>C
ENST00000696771.1:c.174T>C	ENSP00000512860.1:p.Asp58=
ENST00000696772.1:n.2494T>C
ENST00000696773.1:n.2233T>C
ENST00000696774.1:n.6001T>C
ENST00000696776.1:c.984T>C	ENSP00000512861.1:p.Asp328=
ENST00000696777.1:n.2299T>C
ENST00000696778.1:n.1327T>C
ENST00000696779.1:c.498T>C	ENSP00000512862.1:p.Asp166=
ENST00000696780.1:c.921T>C	ENSP00000512863.1:p.Asp307=
ENST00000696781.1:c.636T>C	ENSP00000512864.1:p.Asp212=
ENST00000696782.1:c.*293T>C	ENSP00000512865.1:n.*293T>C
ENST00000696783.1:n.2759T>C
ENST00000696992.1:n.2008T>C
ENST00000696995.1:n.4420T>C
ENST00000696996.1:n.2333T>C
ENST00000696997.1:c.*521T>C	ENSP00000513028.1:n.*521T>C
ENST00000696998.1:n.2145T>C
ENST00000696999.1:c.174T>C	ENSP00000513029.1:p.Asp58=
ENST00000697036.1:c.*307T>C	ENSP00000513060.1:n.*307T>C
ENST00000697037.1:n.926T>C
ENST00000697093.1:n.3127T>C
ENST00000697094.1:n.3474T>C
ENST00000697095.1:c.*2092T>C	ENSP00000513104.1:n.*2092T>C
ENST00000697096.1:n.2024T>C
ENST00000697097.1:c.174T>C	ENSP00000513105.1:p.Asp58=
ENST00000562983.2:n.1077T>C
ENST00000690268.1:c.972T>C	ENSP00000509810.1:p.Asp324=
ENST00000355740.7:c.*217T>C	ENSP00000347979.3:n.*217T>C
ENST00000612663.5:c.*293T>C	ENSP00000477997.3:n.*293T>C
ENST00000640140.1:n.1063T>C
ENST00000640250.1:n.390T>C
ENST00000640681.1:n.1012T>C
ENST00000652046.1:c.891T>C MANE Select	ENSP00000498466.1:p.Asp297=
ENST00000352159.8:c.*208T>C	ENSP00000345601.4:n.*208T>C
ENST00000355279.2:c.866T>C	ENSP00000347426.2:n.866T>C
ENST00000355740.6:c.891T>C	ENSP00000347979.2:p.Asp297=
ENST00000357339.6:c.828T>C	ENSP00000349896.2:p.Asp276=
ENST00000479522.5:c.*320T>C	ENSP00000424113.1:n.*320T>C
ENST00000484444.5:c.*332T>C	ENSP00000420975.1:n.*332T>C
ENST00000488877.5:c.*332T>C	ENSP00000425159.1:n.*332T>C
ENST00000492756.5:c.719T>C	ENSP00000422453.1:n.719T>C
ENST00000494410.5:c.*249T>C	ENSP00000423755.1:n.*249T>C
ENST00000612663.4:c.*238T>C	ENSP00000477997.2:n.*238T>C
NM_000043.4:c.891T>C , LRG_134t1:c.891T>C	NP_000034.1:p.Asp297=
NM_152871.2:c.828T>C	NP_690610.1:p.Asp276=
NM_152872.2:c.*203T>C	NP_690611.1:n.*203T>C
NR_028033.2:n.1065T>C
NR_028034.2:n.927T>C
NR_028035.2:n.990T>C
NR_028036.2:n.1128T>C
XM_006717819.2:c.972T>C	XP_006717882.1:p.Asp324=
XM_011539764.1:c.1053T>C	XP_011538066.1:p.Asp351=
XM_011539765.1:c.990T>C	XP_011538067.1:p.Asp330=
XM_011539766.1:c.972T>C	XP_011538068.1:p.Asp324=
XM_011539767.1:c.936T>C	XP_011538069.1:p.Asp312=
XR_945732.1:n.959T>C
XR_945733.1:n.896T>C
NM_000043.5:c.891T>C	NP_000034.1:p.Asp297=
NM_001320619.1:c.*214T>C	NP_001307548.1:n.*214T>C
NM_152871.3:c.828T>C	NP_690610.1:p.Asp276=
NM_152872.3:c.*203T>C	NP_690611.1:n.*203T>C
NR_028033.3:n.1037T>C
NR_028034.3:n.899T>C
NR_028035.3:n.962T>C
NR_028036.3:n.1100T>C
NR_135313.1:n.1017T>C
NR_135314.1:n.1200T>C
NR_135315.1:n.953T>C
XM_006717819.3:c.972T>C	XP_006717882.1:p.Asp324=
XM_011539764.2:c.1053T>C	XP_011538066.1:p.Asp351=
XM_011539765.2:c.990T>C	XP_011538067.1:p.Asp330=
XM_011539766.2:c.972T>C	XP_011538068.1:p.Asp324=
XM_011539767.3:c.936T>C	XP_011538069.1:p.Asp312=
XR_945732.3:n.959T>C
XR_945733.2:n.896T>C
NM_000043.6:c.891T>C MANE Select	NP_000034.1:p.Asp297=
NM_001320619.2:c.*214T>C	NP_001307548.1:n.*214T>C
NM_152871.4:c.828T>C	NP_690610.1:p.Asp276=
NM_152872.4:c.*203T>C	NP_690611.1:n.*203T>C
NR_028033.4:n.798T>C
NR_028034.4:n.660T>C
NR_028035.4:n.723T>C
NR_028036.4:n.861T>C
NR_135313.2:n.778T>C
NR_135314.2:n.1057T>C
NR_135315.2:n.810T>C