Canonical Allele Identifier: CA377509571

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773894A>C (hg19) ; chr10:g.89014137A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014137A>C , CM000672.2:g.89014137A>C	GRCh38
NC_000010.10:g.90773894A>C , CM000672.1:g.90773894A>C	GRCh37
NC_000010.9:g.90763874A>C	NCBI36
NG_009089.2:g.28607A>C , LRG_134:g.28607A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1004A>C
ENST00000355740.8:c.*18A>C	ENSP00000347979.3:n.*18A>C
ENST00000357339.7:c.632A>C	ENSP00000349896.2:p.Tyr211Ser
ENST00000371857.8:n.2240A>C
ENST00000460510.6:c.-23A>C	ENSP00000512812.1:n.-23A>C
ENST00000466081.6:n.2344A>C
ENST00000477270.6:c.740A>C	ENSP00000512813.1:p.Tyr247Ser
ENST00000479522.6:c.*124A>C	ENSP00000424113.1:n.*124A>C
ENST00000484444.6:c.*136A>C	ENSP00000420975.1:n.*136A>C
ENST00000488877.6:c.586A>C	ENSP00000425159.1:n.586A>C
ENST00000492756.7:c.*124A>C	ENSP00000422453.1:n.*124A>C
ENST00000494799.6:c.-23A>C	ENSP00000512834.1:n.-23A>C
ENST00000562983.3:c.-23A>C	ENSP00000512845.1:n.-23A>C
ENST00000612663.6:c.*97A>C	ENSP00000477997.3:n.*97A>C
ENST00000640140.2:n.840A>C
ENST00000640250.2:n.194A>C
ENST00000640681.2:n.799A>C
ENST00000696723.1:n.4328A>C
ENST00000696741.1:n.2333A>C
ENST00000696742.1:n.2060A>C
ENST00000696743.1:n.3463A>C
ENST00000696744.1:n.734A>C
ENST00000696767.1:n.1029A>C
ENST00000696768.1:c.*18A>C	ENSP00000512859.1:n.*18A>C
ENST00000696769.1:n.2384A>C
ENST00000696771.1:c.-23A>C	ENSP00000512860.1:n.-23A>C
ENST00000696772.1:n.2298A>C
ENST00000696773.1:n.2037A>C
ENST00000696774.1:n.5805A>C
ENST00000696776.1:c.788A>C	ENSP00000512861.1:p.Tyr263Ser
ENST00000696777.1:n.2103A>C
ENST00000696778.1:n.1131A>C
ENST00000696779.1:c.302A>C	ENSP00000512862.1:p.Tyr101Ser
ENST00000696780.1:c.725A>C	ENSP00000512863.1:p.Tyr242Ser
ENST00000696781.1:c.440A>C	ENSP00000512864.1:p.Tyr147Ser
ENST00000696782.1:c.*97A>C	ENSP00000512865.1:n.*97A>C
ENST00000696783.1:n.2563A>C
ENST00000696992.1:n.1812A>C
ENST00000696995.1:n.4224A>C
ENST00000696996.1:n.2137A>C
ENST00000696997.1:c.*325A>C	ENSP00000513028.1:n.*325A>C
ENST00000696998.1:n.1949A>C
ENST00000696999.1:c.-23A>C	ENSP00000513029.1:n.-23A>C
ENST00000697035.1:c.*28A>C	ENSP00000513059.1:n.*28A>C
ENST00000697036.1:c.*111A>C	ENSP00000513060.1:n.*111A>C
ENST00000697037.1:n.730A>C
ENST00000697093.1:n.2931A>C
ENST00000697094.1:n.3278A>C
ENST00000697095.1:c.*1896A>C	ENSP00000513104.1:n.*1896A>C
ENST00000697096.1:n.1828A>C
ENST00000697097.1:c.-23A>C	ENSP00000513105.1:n.-23A>C
ENST00000562983.2:n.881A>C
ENST00000690268.1:c.776A>C	ENSP00000509810.1:p.Tyr259Ser
ENST00000355740.7:c.*21A>C	ENSP00000347979.3:n.*21A>C
ENST00000612663.5:c.*97A>C	ENSP00000477997.3:n.*97A>C
ENST00000640140.1:n.867A>C
ENST00000640250.1:n.194A>C
ENST00000640681.1:n.816A>C
ENST00000652046.1:c.695A>C MANE Select	ENSP00000498466.1:p.Tyr232Ser
ENST00000313771.9:n.1004A>C
ENST00000352159.8:c.*12A>C	ENSP00000345601.4:n.*12A>C
ENST00000355279.2:c.670A>C	ENSP00000347426.2:n.670A>C
ENST00000355740.6:c.695A>C	ENSP00000347979.2:p.Tyr232Ser
ENST00000357339.6:c.632A>C	ENSP00000349896.2:p.Tyr211Ser
ENST00000479522.5:c.*124A>C	ENSP00000424113.1:n.*124A>C
ENST00000484444.5:c.*136A>C	ENSP00000420975.1:n.*136A>C
ENST00000488877.5:c.*136A>C	ENSP00000425159.1:n.*136A>C
ENST00000492756.5:c.523A>C	ENSP00000422453.1:n.523A>C
ENST00000494410.5:c.*53A>C	ENSP00000423755.1:n.*53A>C
ENST00000494799.5:n.602A>C
ENST00000612663.4:c.*42A>C	ENSP00000477997.2:n.*42A>C
ENST00000615406.4:c.695A>C	ENSP00000484575.1:p.Tyr232Ser
ENST00000626542.2:c.695A>C	ENSP00000485876.1:p.Tyr232Ser
NM_000043.4:c.695A>C , LRG_134t1:c.695A>C	NP_000034.1:p.Tyr232Ser
NM_152871.2:c.632A>C	NP_690610.1:p.Tyr211Ser
NM_152872.2:c.*7A>C	NP_690611.1:n.*7A>C
NR_028033.2:n.869A>C
NR_028034.2:n.731A>C
NR_028035.2:n.794A>C
NR_028036.2:n.932A>C
XM_006717819.2:c.776A>C	XP_006717882.1:p.Tyr259Ser
XM_011539764.1:c.857A>C	XP_011538066.1:p.Tyr286Ser
XM_011539765.1:c.794A>C	XP_011538067.1:p.Tyr265Ser
XM_011539766.1:c.776A>C	XP_011538068.1:p.Tyr259Ser
XM_011539767.1:c.740A>C	XP_011538069.1:p.Tyr247Ser
XR_945732.1:n.763A>C
XR_945733.1:n.700A>C
NM_000043.5:c.695A>C	NP_000034.1:p.Tyr232Ser
NM_001320619.1:c.*18A>C	NP_001307548.1:n.*18A>C
NM_152871.3:c.632A>C	NP_690610.1:p.Tyr211Ser
NM_152872.3:c.*7A>C	NP_690611.1:n.*7A>C
NR_028033.3:n.841A>C
NR_028034.3:n.703A>C
NR_028035.3:n.766A>C
NR_028036.3:n.904A>C
NR_135313.1:n.821A>C
NR_135314.1:n.1004A>C
NR_135315.1:n.757A>C
XM_006717819.3:c.776A>C	XP_006717882.1:p.Tyr259Ser
XM_011539764.2:c.857A>C	XP_011538066.1:p.Tyr286Ser
XM_011539765.2:c.794A>C	XP_011538067.1:p.Tyr265Ser
XM_011539766.2:c.776A>C	XP_011538068.1:p.Tyr259Ser
XM_011539767.3:c.740A>C	XP_011538069.1:p.Tyr247Ser
XR_945732.3:n.763A>C
XR_945733.2:n.700A>C
NM_000043.6:c.695A>C MANE Select	NP_000034.1:p.Tyr232Ser
NM_001320619.2:c.*18A>C	NP_001307548.1:n.*18A>C
NM_152871.4:c.632A>C	NP_690610.1:p.Tyr211Ser
NM_152872.4:c.*7A>C	NP_690611.1:n.*7A>C
NR_028033.4:n.602A>C
NR_028034.4:n.464A>C
NR_028035.4:n.527A>C
NR_028036.4:n.665A>C
NR_135313.2:n.582A>C
NR_135314.2:n.861A>C
NR_135315.2:n.614A>C