Canonical Allele Identifier: CA377510083

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774105T>A (hg19) ; chr10:g.89014348T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014348T>A , CM000672.2:g.89014348T>A	GRCh38
NC_000010.10:g.90774105T>A , CM000672.1:g.90774105T>A	GRCh37
NC_000010.9:g.90764085T>A	NCBI36
NG_009089.2:g.28818T>A , LRG_134:g.28818T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1215T>A
ENST00000355740.8:c.*229T>A	ENSP00000347979.3:n.*229T>A
ENST00000357339.7:c.843T>A	ENSP00000349896.2:p.Asn281Lys
ENST00000371857.8:n.2451T>A
ENST00000460510.6:c.189T>A	ENSP00000512812.1:p.Asn63Lys
ENST00000466081.6:n.2555T>A
ENST00000477270.6:c.951T>A	ENSP00000512813.1:p.Asn317Lys
ENST00000479522.6:c.*335T>A	ENSP00000424113.1:n.*335T>A
ENST00000484444.6:c.*347T>A	ENSP00000420975.1:n.*347T>A
ENST00000488877.6:c.797T>A	ENSP00000425159.1:n.797T>A
ENST00000492756.7:c.*335T>A	ENSP00000422453.1:n.*335T>A
ENST00000494799.6:c.189T>A	ENSP00000512834.1:p.Asn63Lys
ENST00000562983.3:c.189T>A	ENSP00000512845.1:p.Asn63Lys
ENST00000612663.6:c.*308T>A	ENSP00000477997.3:n.*308T>A
ENST00000640140.2:n.1051T>A
ENST00000640250.2:n.405T>A
ENST00000640681.2:n.1010T>A
ENST00000696723.1:n.4539T>A
ENST00000696741.1:n.2544T>A
ENST00000696742.1:n.2271T>A
ENST00000696743.1:n.3674T>A
ENST00000696744.1:n.945T>A
ENST00000696767.1:n.1240T>A
ENST00000696768.1:c.*229T>A	ENSP00000512859.1:n.*229T>A
ENST00000696769.1:n.2595T>A
ENST00000696771.1:c.189T>A	ENSP00000512860.1:p.Asn63Lys
ENST00000696772.1:n.2509T>A
ENST00000696773.1:n.2248T>A
ENST00000696774.1:n.6016T>A
ENST00000696776.1:c.999T>A	ENSP00000512861.1:p.Asn333Lys
ENST00000696777.1:n.2314T>A
ENST00000696778.1:n.1342T>A
ENST00000696779.1:c.513T>A	ENSP00000512862.1:p.Asn171Lys
ENST00000696780.1:c.936T>A	ENSP00000512863.1:p.Asn312Lys
ENST00000696781.1:c.651T>A	ENSP00000512864.1:p.Asn217Lys
ENST00000696782.1:c.*308T>A	ENSP00000512865.1:n.*308T>A
ENST00000696783.1:n.2774T>A
ENST00000696992.1:n.2023T>A
ENST00000696995.1:n.4435T>A
ENST00000696996.1:n.2348T>A
ENST00000696997.1:c.*536T>A	ENSP00000513028.1:n.*536T>A
ENST00000696998.1:n.2160T>A
ENST00000696999.1:c.189T>A	ENSP00000513029.1:p.Asn63Lys
ENST00000697036.1:c.*322T>A	ENSP00000513060.1:n.*322T>A
ENST00000697037.1:n.941T>A
ENST00000697093.1:n.3142T>A
ENST00000697094.1:n.3489T>A
ENST00000697095.1:c.*2107T>A	ENSP00000513104.1:n.*2107T>A
ENST00000697096.1:n.2039T>A
ENST00000697097.1:c.189T>A	ENSP00000513105.1:p.Asn63Lys
ENST00000562983.2:n.1092T>A
ENST00000690268.1:c.987T>A	ENSP00000509810.1:p.Asn329Lys
ENST00000355740.7:c.*232T>A	ENSP00000347979.3:n.*232T>A
ENST00000612663.5:c.*308T>A	ENSP00000477997.3:n.*308T>A
ENST00000640140.1:n.1078T>A
ENST00000640250.1:n.405T>A
ENST00000640681.1:n.1027T>A
ENST00000652046.1:c.906T>A MANE Select	ENSP00000498466.1:p.Asn302Lys
ENST00000352159.8:c.*223T>A	ENSP00000345601.4:n.*223T>A
ENST00000355279.2:c.881T>A	ENSP00000347426.2:n.881T>A
ENST00000355740.6:c.906T>A	ENSP00000347979.2:p.Asn302Lys
ENST00000357339.6:c.843T>A	ENSP00000349896.2:p.Asn281Lys
ENST00000479522.5:c.*335T>A	ENSP00000424113.1:n.*335T>A
ENST00000484444.5:c.*347T>A	ENSP00000420975.1:n.*347T>A
ENST00000488877.5:c.*347T>A	ENSP00000425159.1:n.*347T>A
ENST00000492756.5:c.734T>A	ENSP00000422453.1:n.734T>A
ENST00000494410.5:c.*264T>A	ENSP00000423755.1:n.*264T>A
ENST00000612663.4:c.*253T>A	ENSP00000477997.2:n.*253T>A
NM_000043.4:c.906T>A , LRG_134t1:c.906T>A	NP_000034.1:p.Asn302Lys
NM_152871.2:c.843T>A	NP_690610.1:p.Asn281Lys
NM_152872.2:c.*218T>A	NP_690611.1:n.*218T>A
NR_028033.2:n.1080T>A
NR_028034.2:n.942T>A
NR_028035.2:n.1005T>A
NR_028036.2:n.1143T>A
XM_006717819.2:c.987T>A	XP_006717882.1:p.Asn329Lys
XM_011539764.1:c.1068T>A	XP_011538066.1:p.Asn356Lys
XM_011539765.1:c.1005T>A	XP_011538067.1:p.Asn335Lys
XM_011539766.1:c.987T>A	XP_011538068.1:p.Asn329Lys
XM_011539767.1:c.951T>A	XP_011538069.1:p.Asn317Lys
XR_945732.1:n.974T>A
XR_945733.1:n.911T>A
NM_000043.5:c.906T>A	NP_000034.1:p.Asn302Lys
NM_001320619.1:c.*229T>A	NP_001307548.1:n.*229T>A
NM_152871.3:c.843T>A	NP_690610.1:p.Asn281Lys
NM_152872.3:c.*218T>A	NP_690611.1:n.*218T>A
NR_028033.3:n.1052T>A
NR_028034.3:n.914T>A
NR_028035.3:n.977T>A
NR_028036.3:n.1115T>A
NR_135313.1:n.1032T>A
NR_135314.1:n.1215T>A
NR_135315.1:n.968T>A
XM_006717819.3:c.987T>A	XP_006717882.1:p.Asn329Lys
XM_011539764.2:c.1068T>A	XP_011538066.1:p.Asn356Lys
XM_011539765.2:c.1005T>A	XP_011538067.1:p.Asn335Lys
XM_011539766.2:c.987T>A	XP_011538068.1:p.Asn329Lys
XM_011539767.3:c.951T>A	XP_011538069.1:p.Asn317Lys
XR_945732.3:n.974T>A
XR_945733.2:n.911T>A
NM_000043.6:c.906T>A MANE Select	NP_000034.1:p.Asn302Lys
NM_001320619.2:c.*229T>A	NP_001307548.1:n.*229T>A
NM_152871.4:c.843T>A	NP_690610.1:p.Asn281Lys
NM_152872.4:c.*218T>A	NP_690611.1:n.*218T>A
NR_028033.4:n.813T>A
NR_028034.4:n.675T>A
NR_028035.4:n.738T>A
NR_028036.4:n.876T>A
NR_135313.2:n.793T>A
NR_135314.2:n.1072T>A
NR_135315.2:n.825T>A