Canonical Allele Identifier: CA377510014

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774075C>A (hg19) ; chr10:g.89014318C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014318C>A , CM000672.2:g.89014318C>A	GRCh38
NC_000010.10:g.90774075C>A , CM000672.1:g.90774075C>A	GRCh37
NC_000010.9:g.90764055C>A	NCBI36
NG_009089.2:g.28788C>A , LRG_134:g.28788C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1185C>A
ENST00000355740.8:c.*199C>A	ENSP00000347979.3:n.*199C>A
ENST00000357339.7:c.813C>A	ENSP00000349896.2:p.Asp271Glu
ENST00000371857.8:n.2421C>A
ENST00000460510.6:c.159C>A	ENSP00000512812.1:p.Asp53Glu
ENST00000466081.6:n.2525C>A
ENST00000477270.6:c.921C>A	ENSP00000512813.1:p.Asp307Glu
ENST00000479522.6:c.*305C>A	ENSP00000424113.1:n.*305C>A
ENST00000484444.6:c.*317C>A	ENSP00000420975.1:n.*317C>A
ENST00000488877.6:c.767C>A	ENSP00000425159.1:n.767C>A
ENST00000492756.7:c.*305C>A	ENSP00000422453.1:n.*305C>A
ENST00000494799.6:c.159C>A	ENSP00000512834.1:p.Asp53Glu
ENST00000562983.3:c.159C>A	ENSP00000512845.1:p.Asp53Glu
ENST00000612663.6:c.*278C>A	ENSP00000477997.3:n.*278C>A
ENST00000640140.2:n.1021C>A
ENST00000640250.2:n.375C>A
ENST00000640681.2:n.980C>A
ENST00000696723.1:n.4509C>A
ENST00000696741.1:n.2514C>A
ENST00000696742.1:n.2241C>A
ENST00000696743.1:n.3644C>A
ENST00000696744.1:n.915C>A
ENST00000696767.1:n.1210C>A
ENST00000696768.1:c.*199C>A	ENSP00000512859.1:n.*199C>A
ENST00000696769.1:n.2565C>A
ENST00000696771.1:c.159C>A	ENSP00000512860.1:p.Asp53Glu
ENST00000696772.1:n.2479C>A
ENST00000696773.1:n.2218C>A
ENST00000696774.1:n.5986C>A
ENST00000696776.1:c.969C>A	ENSP00000512861.1:p.Asp323Glu
ENST00000696777.1:n.2284C>A
ENST00000696778.1:n.1312C>A
ENST00000696779.1:c.483C>A	ENSP00000512862.1:p.Asp161Glu
ENST00000696780.1:c.906C>A	ENSP00000512863.1:p.Asp302Glu
ENST00000696781.1:c.621C>A	ENSP00000512864.1:p.Asp207Glu
ENST00000696782.1:c.*278C>A	ENSP00000512865.1:n.*278C>A
ENST00000696783.1:n.2744C>A
ENST00000696992.1:n.1993C>A
ENST00000696995.1:n.4405C>A
ENST00000696996.1:n.2318C>A
ENST00000696997.1:c.*506C>A	ENSP00000513028.1:n.*506C>A
ENST00000696998.1:n.2130C>A
ENST00000696999.1:c.159C>A	ENSP00000513029.1:p.Asp53Glu
ENST00000697036.1:c.*292C>A	ENSP00000513060.1:n.*292C>A
ENST00000697037.1:n.911C>A
ENST00000697093.1:n.3112C>A
ENST00000697094.1:n.3459C>A
ENST00000697095.1:c.*2077C>A	ENSP00000513104.1:n.*2077C>A
ENST00000697096.1:n.2009C>A
ENST00000697097.1:c.159C>A	ENSP00000513105.1:p.Asp53Glu
ENST00000562983.2:n.1062C>A
ENST00000690268.1:c.957C>A	ENSP00000509810.1:p.Asp319Glu
ENST00000355740.7:c.*202C>A	ENSP00000347979.3:n.*202C>A
ENST00000612663.5:c.*278C>A	ENSP00000477997.3:n.*278C>A
ENST00000640140.1:n.1048C>A
ENST00000640250.1:n.375C>A
ENST00000640681.1:n.997C>A
ENST00000652046.1:c.876C>A MANE Select	ENSP00000498466.1:p.Asp292Glu
ENST00000352159.8:c.*193C>A	ENSP00000345601.4:n.*193C>A
ENST00000355279.2:c.851C>A	ENSP00000347426.2:n.851C>A
ENST00000355740.6:c.876C>A	ENSP00000347979.2:p.Asp292Glu
ENST00000357339.6:c.813C>A	ENSP00000349896.2:p.Asp271Glu
ENST00000479522.5:c.*305C>A	ENSP00000424113.1:n.*305C>A
ENST00000484444.5:c.*317C>A	ENSP00000420975.1:n.*317C>A
ENST00000488877.5:c.*317C>A	ENSP00000425159.1:n.*317C>A
ENST00000492756.5:c.704C>A	ENSP00000422453.1:n.704C>A
ENST00000494410.5:c.*234C>A	ENSP00000423755.1:n.*234C>A
ENST00000612663.4:c.*223C>A	ENSP00000477997.2:n.*223C>A
NM_000043.4:c.876C>A , LRG_134t1:c.876C>A	NP_000034.1:p.Asp292Glu
NM_152871.2:c.813C>A	NP_690610.1:p.Asp271Glu
NM_152872.2:c.*188C>A	NP_690611.1:n.*188C>A
NR_028033.2:n.1050C>A
NR_028034.2:n.912C>A
NR_028035.2:n.975C>A
NR_028036.2:n.1113C>A
XM_006717819.2:c.957C>A	XP_006717882.1:p.Asp319Glu
XM_011539764.1:c.1038C>A	XP_011538066.1:p.Asp346Glu
XM_011539765.1:c.975C>A	XP_011538067.1:p.Asp325Glu
XM_011539766.1:c.957C>A	XP_011538068.1:p.Asp319Glu
XM_011539767.1:c.921C>A	XP_011538069.1:p.Asp307Glu
XR_945732.1:n.944C>A
XR_945733.1:n.881C>A
NM_000043.5:c.876C>A	NP_000034.1:p.Asp292Glu
NM_001320619.1:c.*199C>A	NP_001307548.1:n.*199C>A
NM_152871.3:c.813C>A	NP_690610.1:p.Asp271Glu
NM_152872.3:c.*188C>A	NP_690611.1:n.*188C>A
NR_028033.3:n.1022C>A
NR_028034.3:n.884C>A
NR_028035.3:n.947C>A
NR_028036.3:n.1085C>A
NR_135313.1:n.1002C>A
NR_135314.1:n.1185C>A
NR_135315.1:n.938C>A
XM_006717819.3:c.957C>A	XP_006717882.1:p.Asp319Glu
XM_011539764.2:c.1038C>A	XP_011538066.1:p.Asp346Glu
XM_011539765.2:c.975C>A	XP_011538067.1:p.Asp325Glu
XM_011539766.2:c.957C>A	XP_011538068.1:p.Asp319Glu
XM_011539767.3:c.921C>A	XP_011538069.1:p.Asp307Glu
XR_945732.3:n.944C>A
XR_945733.2:n.881C>A
NM_000043.6:c.876C>A MANE Select	NP_000034.1:p.Asp292Glu
NM_001320619.2:c.*199C>A	NP_001307548.1:n.*199C>A
NM_152871.4:c.813C>A	NP_690610.1:p.Asp271Glu
NM_152872.4:c.*188C>A	NP_690611.1:n.*188C>A
NR_028033.4:n.783C>A
NR_028034.4:n.645C>A
NR_028035.4:n.708C>A
NR_028036.4:n.846C>A
NR_135313.2:n.763C>A
NR_135314.2:n.1042C>A
NR_135315.2:n.795C>A