Canonical Allele Identifier: CA377509753

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773964T>A (hg19) ; chr10:g.89014207T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014207T>A , CM000672.2:g.89014207T>A	GRCh38
NC_000010.10:g.90773964T>A , CM000672.1:g.90773964T>A	GRCh37
NC_000010.9:g.90763944T>A	NCBI36
NG_009089.2:g.28677T>A , LRG_134:g.28677T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1074T>A
ENST00000355740.8:c.*88T>A	ENSP00000347979.3:n.*88T>A
ENST00000357339.7:c.702T>A	ENSP00000349896.2:p.Asn234Lys
ENST00000371857.8:n.2310T>A
ENST00000460510.6:c.48T>A	ENSP00000512812.1:p.Asn16Lys
ENST00000466081.6:n.2414T>A
ENST00000477270.6:c.810T>A	ENSP00000512813.1:p.Asn270Lys
ENST00000479522.6:c.*194T>A	ENSP00000424113.1:n.*194T>A
ENST00000484444.6:c.*206T>A	ENSP00000420975.1:n.*206T>A
ENST00000488877.6:c.656T>A	ENSP00000425159.1:n.656T>A
ENST00000492756.7:c.*194T>A	ENSP00000422453.1:n.*194T>A
ENST00000494799.6:c.48T>A	ENSP00000512834.1:p.Asn16Lys
ENST00000562983.3:c.48T>A	ENSP00000512845.1:p.Asn16Lys
ENST00000612663.6:c.*167T>A	ENSP00000477997.3:n.*167T>A
ENST00000640140.2:n.910T>A
ENST00000640250.2:n.264T>A
ENST00000640681.2:n.869T>A
ENST00000696723.1:n.4398T>A
ENST00000696741.1:n.2403T>A
ENST00000696742.1:n.2130T>A
ENST00000696743.1:n.3533T>A
ENST00000696744.1:n.804T>A
ENST00000696767.1:n.1099T>A
ENST00000696768.1:c.*88T>A	ENSP00000512859.1:n.*88T>A
ENST00000696769.1:n.2454T>A
ENST00000696771.1:c.48T>A	ENSP00000512860.1:p.Asn16Lys
ENST00000696772.1:n.2368T>A
ENST00000696773.1:n.2107T>A
ENST00000696774.1:n.5875T>A
ENST00000696776.1:c.858T>A	ENSP00000512861.1:p.Asn286Lys
ENST00000696777.1:n.2173T>A
ENST00000696778.1:n.1201T>A
ENST00000696779.1:c.372T>A	ENSP00000512862.1:p.Asn124Lys
ENST00000696780.1:c.795T>A	ENSP00000512863.1:p.Asn265Lys
ENST00000696781.1:c.510T>A	ENSP00000512864.1:p.Asn170Lys
ENST00000696782.1:c.*167T>A	ENSP00000512865.1:n.*167T>A
ENST00000696783.1:n.2633T>A
ENST00000696992.1:n.1882T>A
ENST00000696995.1:n.4294T>A
ENST00000696996.1:n.2207T>A
ENST00000696997.1:c.*395T>A	ENSP00000513028.1:n.*395T>A
ENST00000696998.1:n.2019T>A
ENST00000696999.1:c.48T>A	ENSP00000513029.1:p.Asn16Lys
ENST00000697035.1:c.*98T>A	ENSP00000513059.1:n.*98T>A
ENST00000697036.1:c.*181T>A	ENSP00000513060.1:n.*181T>A
ENST00000697037.1:n.800T>A
ENST00000697093.1:n.3001T>A
ENST00000697094.1:n.3348T>A
ENST00000697095.1:c.*1966T>A	ENSP00000513104.1:n.*1966T>A
ENST00000697096.1:n.1898T>A
ENST00000697097.1:c.48T>A	ENSP00000513105.1:p.Asn16Lys
ENST00000562983.2:n.951T>A
ENST00000690268.1:c.846T>A	ENSP00000509810.1:p.Asn282Lys
ENST00000355740.7:c.*91T>A	ENSP00000347979.3:n.*91T>A
ENST00000612663.5:c.*167T>A	ENSP00000477997.3:n.*167T>A
ENST00000640140.1:n.937T>A
ENST00000640250.1:n.264T>A
ENST00000640681.1:n.886T>A
ENST00000652046.1:c.765T>A MANE Select	ENSP00000498466.1:p.Asn255Lys
ENST00000352159.8:c.*82T>A	ENSP00000345601.4:n.*82T>A
ENST00000355279.2:c.740T>A	ENSP00000347426.2:n.740T>A
ENST00000355740.6:c.765T>A	ENSP00000347979.2:p.Asn255Lys
ENST00000357339.6:c.702T>A	ENSP00000349896.2:p.Asn234Lys
ENST00000479522.5:c.*194T>A	ENSP00000424113.1:n.*194T>A
ENST00000484444.5:c.*206T>A	ENSP00000420975.1:n.*206T>A
ENST00000488877.5:c.*206T>A	ENSP00000425159.1:n.*206T>A
ENST00000492756.5:c.593T>A	ENSP00000422453.1:n.593T>A
ENST00000494410.5:c.*123T>A	ENSP00000423755.1:n.*123T>A
ENST00000494799.5:n.672T>A
ENST00000612663.4:c.*112T>A	ENSP00000477997.2:n.*112T>A
ENST00000615406.4:c.763T>A	ENSP00000484575.1:p.Ter255Arg
NM_000043.4:c.765T>A , LRG_134t1:c.765T>A	NP_000034.1:p.Asn255Lys
NM_152871.2:c.702T>A	NP_690610.1:p.Asn234Lys
NM_152872.2:c.*77T>A	NP_690611.1:n.*77T>A
NR_028033.2:n.939T>A
NR_028034.2:n.801T>A
NR_028035.2:n.864T>A
NR_028036.2:n.1002T>A
XM_006717819.2:c.846T>A	XP_006717882.1:p.Asn282Lys
XM_011539764.1:c.927T>A	XP_011538066.1:p.Asn309Lys
XM_011539765.1:c.864T>A	XP_011538067.1:p.Asn288Lys
XM_011539766.1:c.846T>A	XP_011538068.1:p.Asn282Lys
XM_011539767.1:c.810T>A	XP_011538069.1:p.Asn270Lys
XR_945732.1:n.833T>A
XR_945733.1:n.770T>A
NM_000043.5:c.765T>A	NP_000034.1:p.Asn255Lys
NM_001320619.1:c.*88T>A	NP_001307548.1:n.*88T>A
NM_152871.3:c.702T>A	NP_690610.1:p.Asn234Lys
NM_152872.3:c.*77T>A	NP_690611.1:n.*77T>A
NR_028033.3:n.911T>A
NR_028034.3:n.773T>A
NR_028035.3:n.836T>A
NR_028036.3:n.974T>A
NR_135313.1:n.891T>A
NR_135314.1:n.1074T>A
NR_135315.1:n.827T>A
XM_006717819.3:c.846T>A	XP_006717882.1:p.Asn282Lys
XM_011539764.2:c.927T>A	XP_011538066.1:p.Asn309Lys
XM_011539765.2:c.864T>A	XP_011538067.1:p.Asn288Lys
XM_011539766.2:c.846T>A	XP_011538068.1:p.Asn282Lys
XM_011539767.3:c.810T>A	XP_011538069.1:p.Asn270Lys
XR_945732.3:n.833T>A
XR_945733.2:n.770T>A
NM_000043.6:c.765T>A MANE Select	NP_000034.1:p.Asn255Lys
NM_001320619.2:c.*88T>A	NP_001307548.1:n.*88T>A
NM_152871.4:c.702T>A	NP_690610.1:p.Asn234Lys
NM_152872.4:c.*77T>A	NP_690611.1:n.*77T>A
NR_028033.4:n.672T>A
NR_028034.4:n.534T>A
NR_028035.4:n.597T>A
NR_028036.4:n.735T>A
NR_135313.2:n.652T>A
NR_135314.2:n.931T>A
NR_135315.2:n.684T>A