Canonical Allele Identifier: CA377510246

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774179T>C (hg19) ; chr10:g.89014422T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014422T>C , CM000672.2:g.89014422T>C	GRCh38
NC_000010.10:g.90774179T>C , CM000672.1:g.90774179T>C	GRCh37
NC_000010.9:g.90764159T>C	NCBI36
NG_009089.2:g.28892T>C , LRG_134:g.28892T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1289T>C
ENST00000355740.8:c.*303T>C	ENSP00000347979.3:n.*303T>C
ENST00000357339.7:c.917T>C	ENSP00000349896.2:p.Phe306Ser
ENST00000371857.8:n.2525T>C
ENST00000460510.6:c.263T>C	ENSP00000512812.1:p.Phe88Ser
ENST00000466081.6:n.2629T>C
ENST00000477270.6:c.1025T>C	ENSP00000512813.1:p.Phe342Ser
ENST00000479522.6:c.*409T>C	ENSP00000424113.1:n.*409T>C
ENST00000484444.6:c.*421T>C	ENSP00000420975.1:n.*421T>C
ENST00000488877.6:c.871T>C	ENSP00000425159.1:n.871T>C
ENST00000492756.7:c.*409T>C	ENSP00000422453.1:n.*409T>C
ENST00000494799.6:c.263T>C	ENSP00000512834.1:p.Phe88Ser
ENST00000562983.3:c.263T>C	ENSP00000512845.1:p.Phe88Ser
ENST00000612663.6:c.*382T>C	ENSP00000477997.3:n.*382T>C
ENST00000640140.2:n.1125T>C
ENST00000640250.2:n.479T>C
ENST00000640681.2:n.1084T>C
ENST00000696723.1:n.4613T>C
ENST00000696741.1:n.2618T>C
ENST00000696742.1:n.2345T>C
ENST00000696743.1:n.3748T>C
ENST00000696744.1:n.1019T>C
ENST00000696767.1:n.1314T>C
ENST00000696768.1:c.*303T>C	ENSP00000512859.1:n.*303T>C
ENST00000696769.1:n.2669T>C
ENST00000696771.1:c.263T>C	ENSP00000512860.1:p.Phe88Ser
ENST00000696772.1:n.2583T>C
ENST00000696773.1:n.2322T>C
ENST00000696774.1:n.6090T>C
ENST00000696776.1:c.1073T>C	ENSP00000512861.1:p.Phe358Ser
ENST00000696777.1:n.2388T>C
ENST00000696778.1:n.1416T>C
ENST00000696779.1:c.587T>C	ENSP00000512862.1:p.Phe196Ser
ENST00000696780.1:c.1010T>C	ENSP00000512863.1:p.Phe337Ser
ENST00000696781.1:c.725T>C	ENSP00000512864.1:p.Phe242Ser
ENST00000696782.1:c.*382T>C	ENSP00000512865.1:n.*382T>C
ENST00000696783.1:n.2848T>C
ENST00000696992.1:n.2097T>C
ENST00000696995.1:n.4509T>C
ENST00000696996.1:n.2422T>C
ENST00000696997.1:c.*610T>C	ENSP00000513028.1:n.*610T>C
ENST00000696998.1:n.2234T>C
ENST00000696999.1:c.263T>C	ENSP00000513029.1:p.Phe88Ser
ENST00000697036.1:c.*396T>C	ENSP00000513060.1:n.*396T>C
ENST00000697037.1:n.1015T>C
ENST00000697093.1:n.3216T>C
ENST00000697094.1:n.3563T>C
ENST00000697095.1:c.*2181T>C	ENSP00000513104.1:n.*2181T>C
ENST00000697096.1:n.2113T>C
ENST00000697097.1:c.263T>C	ENSP00000513105.1:p.Phe88Ser
ENST00000562983.2:n.1166T>C
ENST00000690268.1:c.1061T>C	ENSP00000509810.1:p.Phe354Ser
ENST00000355740.7:c.*306T>C	ENSP00000347979.3:n.*306T>C
ENST00000612663.5:c.*382T>C	ENSP00000477997.3:n.*382T>C
ENST00000640140.1:n.1152T>C
ENST00000640250.1:n.479T>C
ENST00000640681.1:n.1101T>C
ENST00000652046.1:c.980T>C MANE Select	ENSP00000498466.1:p.Phe327Ser
ENST00000352159.8:c.*297T>C	ENSP00000345601.4:n.*297T>C
ENST00000355279.2:c.955T>C	ENSP00000347426.2:n.955T>C
ENST00000355740.6:c.980T>C	ENSP00000347979.2:p.Phe327Ser
ENST00000357339.6:c.917T>C	ENSP00000349896.2:p.Phe306Ser
ENST00000479522.5:c.*409T>C	ENSP00000424113.1:n.*409T>C
ENST00000484444.5:c.*421T>C	ENSP00000420975.1:n.*421T>C
ENST00000488877.5:c.*421T>C	ENSP00000425159.1:n.*421T>C
ENST00000492756.5:c.808T>C	ENSP00000422453.1:n.808T>C
ENST00000494410.5:c.*338T>C	ENSP00000423755.1:n.*338T>C
ENST00000612663.4:c.*327T>C	ENSP00000477997.2:n.*327T>C
NM_000043.4:c.980T>C , LRG_134t1:c.980T>C	NP_000034.1:p.Phe327Ser
NM_152871.2:c.917T>C	NP_690610.1:p.Phe306Ser
NM_152872.2:c.*292T>C	NP_690611.1:n.*292T>C
NR_028033.2:n.1154T>C
NR_028034.2:n.1016T>C
NR_028035.2:n.1079T>C
NR_028036.2:n.1217T>C
XM_006717819.2:c.1061T>C	XP_006717882.1:p.Phe354Ser
XM_011539764.1:c.1142T>C	XP_011538066.1:p.Phe381Ser
XM_011539765.1:c.1079T>C	XP_011538067.1:p.Phe360Ser
XM_011539766.1:c.1061T>C	XP_011538068.1:p.Phe354Ser
XM_011539767.1:c.1025T>C	XP_011538069.1:p.Phe342Ser
XR_945733.1:n.985T>C
NM_000043.5:c.980T>C	NP_000034.1:p.Phe327Ser
NM_001320619.1:c.*303T>C	NP_001307548.1:n.*303T>C
NM_152871.3:c.917T>C	NP_690610.1:p.Phe306Ser
NM_152872.3:c.*292T>C	NP_690611.1:n.*292T>C
NR_028033.3:n.1126T>C
NR_028034.3:n.988T>C
NR_028035.3:n.1051T>C
NR_028036.3:n.1189T>C
NR_135313.1:n.1106T>C
NR_135314.1:n.1289T>C
NR_135315.1:n.1042T>C
XM_006717819.3:c.1061T>C	XP_006717882.1:p.Phe354Ser
XM_011539764.2:c.1142T>C	XP_011538066.1:p.Phe381Ser
XM_011539765.2:c.1079T>C	XP_011538067.1:p.Phe360Ser
XM_011539766.2:c.1061T>C	XP_011538068.1:p.Phe354Ser
XM_011539767.3:c.1025T>C	XP_011538069.1:p.Phe342Ser
XR_945732.3:n.1048T>C
XR_945733.2:n.985T>C
NM_000043.6:c.980T>C MANE Select	NP_000034.1:p.Phe327Ser
NM_001320619.2:c.*303T>C	NP_001307548.1:n.*303T>C
NM_152871.4:c.917T>C	NP_690610.1:p.Phe306Ser
NM_152872.4:c.*292T>C	NP_690611.1:n.*292T>C
NR_028033.4:n.887T>C
NR_028034.4:n.749T>C
NR_028035.4:n.812T>C
NR_028036.4:n.950T>C
NR_135313.2:n.867T>C
NR_135314.2:n.1146T>C
NR_135315.2:n.899T>C