Canonical Allele Identifier: CA377509998

Gene: FAS

Linked Data

• dbSNP Id: rs2119447036
• MyVariant Identifiers: chr10:g.90774067G>A (hg19) ; chr10:g.89014310G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014310G>A , CM000672.2:g.89014310G>A	GRCh38
NC_000010.10:g.90774067G>A , CM000672.1:g.90774067G>A	GRCh37
NC_000010.9:g.90764047G>A	NCBI36
NG_009089.2:g.28780G>A , LRG_134:g.28780G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1177G>A
ENST00000355740.8:c.*191G>A	ENSP00000347979.3:n.*191G>A
ENST00000357339.7:c.805G>A	ENSP00000349896.2:p.Ala269Thr
ENST00000371857.8:n.2413G>A
ENST00000460510.6:c.151G>A	ENSP00000512812.1:p.Ala51Thr
ENST00000466081.6:n.2517G>A
ENST00000477270.6:c.913G>A	ENSP00000512813.1:p.Ala305Thr
ENST00000479522.6:c.*297G>A	ENSP00000424113.1:n.*297G>A
ENST00000484444.6:c.*309G>A	ENSP00000420975.1:n.*309G>A
ENST00000488877.6:c.759G>A	ENSP00000425159.1:n.759G>A
ENST00000492756.7:c.*297G>A	ENSP00000422453.1:n.*297G>A
ENST00000494799.6:c.151G>A	ENSP00000512834.1:p.Ala51Thr
ENST00000562983.3:c.151G>A	ENSP00000512845.1:p.Ala51Thr
ENST00000612663.6:c.*270G>A	ENSP00000477997.3:n.*270G>A
ENST00000640140.2:n.1013G>A
ENST00000640250.2:n.367G>A
ENST00000640681.2:n.972G>A
ENST00000696723.1:n.4501G>A
ENST00000696741.1:n.2506G>A
ENST00000696742.1:n.2233G>A
ENST00000696743.1:n.3636G>A
ENST00000696744.1:n.907G>A
ENST00000696767.1:n.1202G>A
ENST00000696768.1:c.*191G>A	ENSP00000512859.1:n.*191G>A
ENST00000696769.1:n.2557G>A
ENST00000696771.1:c.151G>A	ENSP00000512860.1:p.Ala51Thr
ENST00000696772.1:n.2471G>A
ENST00000696773.1:n.2210G>A
ENST00000696774.1:n.5978G>A
ENST00000696776.1:c.961G>A	ENSP00000512861.1:p.Ala321Thr
ENST00000696777.1:n.2276G>A
ENST00000696778.1:n.1304G>A
ENST00000696779.1:c.475G>A	ENSP00000512862.1:p.Ala159Thr
ENST00000696780.1:c.898G>A	ENSP00000512863.1:p.Ala300Thr
ENST00000696781.1:c.613G>A	ENSP00000512864.1:p.Ala205Thr
ENST00000696782.1:c.*270G>A	ENSP00000512865.1:n.*270G>A
ENST00000696783.1:n.2736G>A
ENST00000696992.1:n.1985G>A
ENST00000696995.1:n.4397G>A
ENST00000696996.1:n.2310G>A
ENST00000696997.1:c.*498G>A	ENSP00000513028.1:n.*498G>A
ENST00000696998.1:n.2122G>A
ENST00000696999.1:c.151G>A	ENSP00000513029.1:p.Ala51Thr
ENST00000697036.1:c.*284G>A	ENSP00000513060.1:n.*284G>A
ENST00000697037.1:n.903G>A
ENST00000697093.1:n.3104G>A
ENST00000697094.1:n.3451G>A
ENST00000697095.1:c.*2069G>A	ENSP00000513104.1:n.*2069G>A
ENST00000697096.1:n.2001G>A
ENST00000697097.1:c.151G>A	ENSP00000513105.1:p.Ala51Thr
ENST00000562983.2:n.1054G>A
ENST00000690268.1:c.949G>A	ENSP00000509810.1:p.Ala317Thr
ENST00000355740.7:c.*194G>A	ENSP00000347979.3:n.*194G>A
ENST00000612663.5:c.*270G>A	ENSP00000477997.3:n.*270G>A
ENST00000640140.1:n.1040G>A
ENST00000640250.1:n.367G>A
ENST00000640681.1:n.989G>A
ENST00000652046.1:c.868G>A MANE Select	ENSP00000498466.1:p.Ala290Thr
ENST00000352159.8:c.*185G>A	ENSP00000345601.4:n.*185G>A
ENST00000355279.2:c.843G>A	ENSP00000347426.2:n.843G>A
ENST00000355740.6:c.868G>A	ENSP00000347979.2:p.Ala290Thr
ENST00000357339.6:c.805G>A	ENSP00000349896.2:p.Ala269Thr
ENST00000479522.5:c.*297G>A	ENSP00000424113.1:n.*297G>A
ENST00000484444.5:c.*309G>A	ENSP00000420975.1:n.*309G>A
ENST00000488877.5:c.*309G>A	ENSP00000425159.1:n.*309G>A
ENST00000492756.5:c.696G>A	ENSP00000422453.1:n.696G>A
ENST00000494410.5:c.*226G>A	ENSP00000423755.1:n.*226G>A
ENST00000612663.4:c.*215G>A	ENSP00000477997.2:n.*215G>A
NM_000043.4:c.868G>A , LRG_134t1:c.868G>A	NP_000034.1:p.Ala290Thr
NM_152871.2:c.805G>A	NP_690610.1:p.Ala269Thr
NM_152872.2:c.*180G>A	NP_690611.1:n.*180G>A
NR_028033.2:n.1042G>A
NR_028034.2:n.904G>A
NR_028035.2:n.967G>A
NR_028036.2:n.1105G>A
XM_006717819.2:c.949G>A	XP_006717882.1:p.Ala317Thr
XM_011539764.1:c.1030G>A	XP_011538066.1:p.Ala344Thr
XM_011539765.1:c.967G>A	XP_011538067.1:p.Ala323Thr
XM_011539766.1:c.949G>A	XP_011538068.1:p.Ala317Thr
XM_011539767.1:c.913G>A	XP_011538069.1:p.Ala305Thr
XR_945732.1:n.936G>A
XR_945733.1:n.873G>A
NM_000043.5:c.868G>A	NP_000034.1:p.Ala290Thr
NM_001320619.1:c.*191G>A	NP_001307548.1:n.*191G>A
NM_152871.3:c.805G>A	NP_690610.1:p.Ala269Thr
NM_152872.3:c.*180G>A	NP_690611.1:n.*180G>A
NR_028033.3:n.1014G>A
NR_028034.3:n.876G>A
NR_028035.3:n.939G>A
NR_028036.3:n.1077G>A
NR_135313.1:n.994G>A
NR_135314.1:n.1177G>A
NR_135315.1:n.930G>A
XM_006717819.3:c.949G>A	XP_006717882.1:p.Ala317Thr
XM_011539764.2:c.1030G>A	XP_011538066.1:p.Ala344Thr
XM_011539765.2:c.967G>A	XP_011538067.1:p.Ala323Thr
XM_011539766.2:c.949G>A	XP_011538068.1:p.Ala317Thr
XM_011539767.3:c.913G>A	XP_011538069.1:p.Ala305Thr
XR_945732.3:n.936G>A
XR_945733.2:n.873G>A
NM_000043.6:c.868G>A MANE Select	NP_000034.1:p.Ala290Thr
NM_001320619.2:c.*191G>A	NP_001307548.1:n.*191G>A
NM_152871.4:c.805G>A	NP_690610.1:p.Ala269Thr
NM_152872.4:c.*180G>A	NP_690611.1:n.*180G>A
NR_028033.4:n.775G>A
NR_028034.4:n.637G>A
NR_028035.4:n.700G>A
NR_028036.4:n.838G>A
NR_135313.2:n.755G>A
NR_135314.2:n.1034G>A
NR_135315.2:n.787G>A