Canonical Allele Identifier: CA377509997

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774067G>T (hg19) ; chr10:g.89014310G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1177G>T
ENST00000355740.8:c.*191G>T	ENSP00000347979.3:n.*191G>T
ENST00000357339.7:c.805G>T	ENSP00000349896.2:p.Ala269Ser
ENST00000371857.8:n.2413G>T
ENST00000460510.6:c.151G>T	ENSP00000512812.1:p.Ala51Ser
ENST00000466081.6:n.2517G>T
ENST00000477270.6:c.913G>T	ENSP00000512813.1:p.Ala305Ser
ENST00000479522.6:c.*297G>T	ENSP00000424113.1:n.*297G>T
ENST00000484444.6:c.*309G>T	ENSP00000420975.1:n.*309G>T
ENST00000488877.6:c.759G>T	ENSP00000425159.1:n.759G>T
ENST00000492756.7:c.*297G>T	ENSP00000422453.1:n.*297G>T
ENST00000494799.6:c.151G>T	ENSP00000512834.1:p.Ala51Ser
ENST00000562983.3:c.151G>T	ENSP00000512845.1:p.Ala51Ser
ENST00000612663.6:c.*270G>T	ENSP00000477997.3:n.*270G>T
ENST00000640140.2:n.1013G>T
ENST00000640250.2:n.367G>T
ENST00000640681.2:n.972G>T
ENST00000696723.1:n.4501G>T
ENST00000696741.1:n.2506G>T
ENST00000696742.1:n.2233G>T
ENST00000696743.1:n.3636G>T
ENST00000696744.1:n.907G>T
ENST00000696767.1:n.1202G>T
ENST00000696768.1:c.*191G>T	ENSP00000512859.1:n.*191G>T
ENST00000696769.1:n.2557G>T
ENST00000696771.1:c.151G>T	ENSP00000512860.1:p.Ala51Ser
ENST00000696772.1:n.2471G>T
ENST00000696773.1:n.2210G>T
ENST00000696774.1:n.5978G>T
ENST00000696776.1:c.961G>T	ENSP00000512861.1:p.Ala321Ser
ENST00000696777.1:n.2276G>T
ENST00000696778.1:n.1304G>T
ENST00000696779.1:c.475G>T	ENSP00000512862.1:p.Ala159Ser
ENST00000696780.1:c.898G>T	ENSP00000512863.1:p.Ala300Ser
ENST00000696781.1:c.613G>T	ENSP00000512864.1:p.Ala205Ser
ENST00000696782.1:c.*270G>T	ENSP00000512865.1:n.*270G>T
ENST00000696783.1:n.2736G>T
ENST00000696992.1:n.1985G>T
ENST00000696995.1:n.4397G>T
ENST00000696996.1:n.2310G>T
ENST00000696997.1:c.*498G>T	ENSP00000513028.1:n.*498G>T
ENST00000696998.1:n.2122G>T
ENST00000696999.1:c.151G>T	ENSP00000513029.1:p.Ala51Ser
ENST00000697036.1:c.*284G>T	ENSP00000513060.1:n.*284G>T
ENST00000697037.1:n.903G>T
ENST00000697093.1:n.3104G>T
ENST00000697094.1:n.3451G>T
ENST00000697095.1:c.*2069G>T	ENSP00000513104.1:n.*2069G>T
ENST00000697096.1:n.2001G>T
ENST00000697097.1:c.151G>T	ENSP00000513105.1:p.Ala51Ser
ENST00000562983.2:n.1054G>T
ENST00000690268.1:c.949G>T	ENSP00000509810.1:p.Ala317Ser
ENST00000355740.7:c.*194G>T	ENSP00000347979.3:n.*194G>T
ENST00000612663.5:c.*270G>T	ENSP00000477997.3:n.*270G>T
ENST00000640140.1:n.1040G>T
ENST00000640250.1:n.367G>T
ENST00000640681.1:n.989G>T
ENST00000652046.1:c.868G>T MANE Select	ENSP00000498466.1:p.Ala290Ser
ENST00000352159.8:c.*185G>T	ENSP00000345601.4:n.*185G>T
ENST00000355279.2:c.843G>T	ENSP00000347426.2:n.843G>T
ENST00000355740.6:c.868G>T	ENSP00000347979.2:p.Ala290Ser
ENST00000357339.6:c.805G>T	ENSP00000349896.2:p.Ala269Ser
ENST00000479522.5:c.*297G>T	ENSP00000424113.1:n.*297G>T
ENST00000484444.5:c.*309G>T	ENSP00000420975.1:n.*309G>T
ENST00000488877.5:c.*309G>T	ENSP00000425159.1:n.*309G>T
ENST00000492756.5:c.696G>T	ENSP00000422453.1:n.696G>T
ENST00000494410.5:c.*226G>T	ENSP00000423755.1:n.*226G>T
ENST00000612663.4:c.*215G>T	ENSP00000477997.2:n.*215G>T
NM_000043.4:c.868G>T , LRG_134t1:c.868G>T	NP_000034.1:p.Ala290Ser
NM_152871.2:c.805G>T	NP_690610.1:p.Ala269Ser
NM_152872.2:c.*180G>T	NP_690611.1:n.*180G>T
NR_028033.2:n.1042G>T
NR_028034.2:n.904G>T
NR_028035.2:n.967G>T
NR_028036.2:n.1105G>T
XM_006717819.2:c.949G>T	XP_006717882.1:p.Ala317Ser
XM_011539764.1:c.1030G>T	XP_011538066.1:p.Ala344Ser
XM_011539765.1:c.967G>T	XP_011538067.1:p.Ala323Ser
XM_011539766.1:c.949G>T	XP_011538068.1:p.Ala317Ser
XM_011539767.1:c.913G>T	XP_011538069.1:p.Ala305Ser
XR_945732.1:n.936G>T
XR_945733.1:n.873G>T
NM_000043.5:c.868G>T	NP_000034.1:p.Ala290Ser
NM_001320619.1:c.*191G>T	NP_001307548.1:n.*191G>T
NM_152871.3:c.805G>T	NP_690610.1:p.Ala269Ser
NM_152872.3:c.*180G>T	NP_690611.1:n.*180G>T
NR_028033.3:n.1014G>T
NR_028034.3:n.876G>T
NR_028035.3:n.939G>T
NR_028036.3:n.1077G>T
NR_135313.1:n.994G>T
NR_135314.1:n.1177G>T
NR_135315.1:n.930G>T
XM_006717819.3:c.949G>T	XP_006717882.1:p.Ala317Ser
XM_011539764.2:c.1030G>T	XP_011538066.1:p.Ala344Ser
XM_011539765.2:c.967G>T	XP_011538067.1:p.Ala323Ser
XM_011539766.2:c.949G>T	XP_011538068.1:p.Ala317Ser
XM_011539767.3:c.913G>T	XP_011538069.1:p.Ala305Ser
XR_945732.3:n.936G>T
XR_945733.2:n.873G>T
NM_000043.6:c.868G>T MANE Select	NP_000034.1:p.Ala290Ser
NM_001320619.2:c.*191G>T	NP_001307548.1:n.*191G>T
NM_152871.4:c.805G>T	NP_690610.1:p.Ala269Ser
NM_152872.4:c.*180G>T	NP_690611.1:n.*180G>T
NR_028033.4:n.775G>T
NR_028034.4:n.637G>T
NR_028035.4:n.700G>T
NR_028036.4:n.838G>T
NR_135313.2:n.755G>T
NR_135314.2:n.1034G>T
NR_135315.2:n.787G>T