Canonical Allele Identifier: CA470974935

Gene: FAS

Linked Data

• dbSNP Id: rs1848684983
• gnomAD v3: 10-89014354-T-C
• gnomAD v4: 10-89014354-T-C
• MyVariant Identifiers: chr10:g.90774111T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014354T>C , CM000672.2:g.89014354T>C	GRCh38
NC_000010.10:g.90774111T>C , CM000672.1:g.90774111T>C	GRCh37
NC_000010.9:g.90764091T>C	NCBI36
NG_009089.2:g.28824T>C , LRG_134:g.28824T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1221T>C
ENST00000355740.8:c.*235T>C	ENSP00000347979.3:n.*235T>C
ENST00000357339.7:c.849T>C	ENSP00000349896.2:p.Cys283=
ENST00000371857.8:n.2457T>C
ENST00000460510.6:c.195T>C	ENSP00000512812.1:p.Cys65=
ENST00000466081.6:n.2561T>C
ENST00000477270.6:c.957T>C	ENSP00000512813.1:p.Cys319=
ENST00000479522.6:c.*341T>C	ENSP00000424113.1:n.*341T>C
ENST00000484444.6:c.*353T>C	ENSP00000420975.1:n.*353T>C
ENST00000488877.6:c.803T>C	ENSP00000425159.1:n.803T>C
ENST00000492756.7:c.*341T>C	ENSP00000422453.1:n.*341T>C
ENST00000494799.6:c.195T>C	ENSP00000512834.1:p.Cys65=
ENST00000562983.3:c.195T>C	ENSP00000512845.1:p.Cys65=
ENST00000612663.6:c.*314T>C	ENSP00000477997.3:n.*314T>C
ENST00000640140.2:n.1057T>C
ENST00000640250.2:n.411T>C
ENST00000640681.2:n.1016T>C
ENST00000696723.1:n.4545T>C
ENST00000696741.1:n.2550T>C
ENST00000696742.1:n.2277T>C
ENST00000696743.1:n.3680T>C
ENST00000696744.1:n.951T>C
ENST00000696767.1:n.1246T>C
ENST00000696768.1:c.*235T>C	ENSP00000512859.1:n.*235T>C
ENST00000696769.1:n.2601T>C
ENST00000696771.1:c.195T>C	ENSP00000512860.1:p.Cys65=
ENST00000696772.1:n.2515T>C
ENST00000696773.1:n.2254T>C
ENST00000696774.1:n.6022T>C
ENST00000696776.1:c.1005T>C	ENSP00000512861.1:p.Cys335=
ENST00000696777.1:n.2320T>C
ENST00000696778.1:n.1348T>C
ENST00000696779.1:c.519T>C	ENSP00000512862.1:p.Cys173=
ENST00000696780.1:c.942T>C	ENSP00000512863.1:p.Cys314=
ENST00000696781.1:c.657T>C	ENSP00000512864.1:p.Cys219=
ENST00000696782.1:c.*314T>C	ENSP00000512865.1:n.*314T>C
ENST00000696783.1:n.2780T>C
ENST00000696992.1:n.2029T>C
ENST00000696995.1:n.4441T>C
ENST00000696996.1:n.2354T>C
ENST00000696997.1:c.*542T>C	ENSP00000513028.1:n.*542T>C
ENST00000696998.1:n.2166T>C
ENST00000696999.1:c.195T>C	ENSP00000513029.1:p.Cys65=
ENST00000697036.1:c.*328T>C	ENSP00000513060.1:n.*328T>C
ENST00000697037.1:n.947T>C
ENST00000697093.1:n.3148T>C
ENST00000697094.1:n.3495T>C
ENST00000697095.1:c.*2113T>C	ENSP00000513104.1:n.*2113T>C
ENST00000697096.1:n.2045T>C
ENST00000697097.1:c.195T>C	ENSP00000513105.1:p.Cys65=
ENST00000562983.2:n.1098T>C
ENST00000690268.1:c.993T>C	ENSP00000509810.1:p.Cys331=
ENST00000355740.7:c.*238T>C	ENSP00000347979.3:n.*238T>C
ENST00000612663.5:c.*314T>C	ENSP00000477997.3:n.*314T>C
ENST00000640140.1:n.1084T>C
ENST00000640250.1:n.411T>C
ENST00000640681.1:n.1033T>C
ENST00000652046.1:c.912T>C MANE Select	ENSP00000498466.1:p.Cys304=
ENST00000352159.8:c.*229T>C	ENSP00000345601.4:n.*229T>C
ENST00000355279.2:c.887T>C	ENSP00000347426.2:n.887T>C
ENST00000355740.6:c.912T>C	ENSP00000347979.2:p.Cys304=
ENST00000357339.6:c.849T>C	ENSP00000349896.2:p.Cys283=
ENST00000479522.5:c.*341T>C	ENSP00000424113.1:n.*341T>C
ENST00000484444.5:c.*353T>C	ENSP00000420975.1:n.*353T>C
ENST00000488877.5:c.*353T>C	ENSP00000425159.1:n.*353T>C
ENST00000492756.5:c.740T>C	ENSP00000422453.1:n.740T>C
ENST00000494410.5:c.*270T>C	ENSP00000423755.1:n.*270T>C
ENST00000612663.4:c.*259T>C	ENSP00000477997.2:n.*259T>C
NM_000043.4:c.912T>C , LRG_134t1:c.912T>C	NP_000034.1:p.Cys304=
NM_152871.2:c.849T>C	NP_690610.1:p.Cys283=
NM_152872.2:c.*224T>C	NP_690611.1:n.*224T>C
NR_028033.2:n.1086T>C
NR_028034.2:n.948T>C
NR_028035.2:n.1011T>C
NR_028036.2:n.1149T>C
XM_006717819.2:c.993T>C	XP_006717882.1:p.Cys331=
XM_011539764.1:c.1074T>C	XP_011538066.1:p.Cys358=
XM_011539765.1:c.1011T>C	XP_011538067.1:p.Cys337=
XM_011539766.1:c.993T>C	XP_011538068.1:p.Cys331=
XM_011539767.1:c.957T>C	XP_011538069.1:p.Cys319=
XR_945732.1:n.980T>C
XR_945733.1:n.917T>C
NM_000043.5:c.912T>C	NP_000034.1:p.Cys304=
NM_001320619.1:c.*235T>C	NP_001307548.1:n.*235T>C
NM_152871.3:c.849T>C	NP_690610.1:p.Cys283=
NM_152872.3:c.*224T>C	NP_690611.1:n.*224T>C
NR_028033.3:n.1058T>C
NR_028034.3:n.920T>C
NR_028035.3:n.983T>C
NR_028036.3:n.1121T>C
NR_135313.1:n.1038T>C
NR_135314.1:n.1221T>C
NR_135315.1:n.974T>C
XM_006717819.3:c.993T>C	XP_006717882.1:p.Cys331=
XM_011539764.2:c.1074T>C	XP_011538066.1:p.Cys358=
XM_011539765.2:c.1011T>C	XP_011538067.1:p.Cys337=
XM_011539766.2:c.993T>C	XP_011538068.1:p.Cys331=
XM_011539767.3:c.957T>C	XP_011538069.1:p.Cys319=
XR_945732.3:n.980T>C
XR_945733.2:n.917T>C
NM_000043.6:c.912T>C MANE Select	NP_000034.1:p.Cys304=
NM_001320619.2:c.*235T>C	NP_001307548.1:n.*235T>C
NM_152871.4:c.849T>C	NP_690610.1:p.Cys283=
NM_152872.4:c.*224T>C	NP_690611.1:n.*224T>C
NR_028033.4:n.819T>C
NR_028034.4:n.681T>C
NR_028035.4:n.744T>C
NR_028036.4:n.882T>C
NR_135313.2:n.799T>C
NR_135314.2:n.1078T>C
NR_135315.2:n.831T>C