Canonical Allele Identifier: CA377510139

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774130C>T (hg19) ; chr10:g.89014373C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014373C>T , CM000672.2:g.89014373C>T	GRCh38
NC_000010.10:g.90774130C>T , CM000672.1:g.90774130C>T	GRCh37
NC_000010.9:g.90764110C>T	NCBI36
NG_009089.2:g.28843C>T , LRG_134:g.28843C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1240C>T
ENST00000355740.8:c.*254C>T	ENSP00000347979.3:n.*254C>T
ENST00000357339.7:c.868C>T	ENSP00000349896.2:p.Gln290Ter
ENST00000371857.8:n.2476C>T
ENST00000460510.6:c.214C>T	ENSP00000512812.1:p.Gln72Ter
ENST00000466081.6:n.2580C>T
ENST00000477270.6:c.976C>T	ENSP00000512813.1:p.Gln326Ter
ENST00000479522.6:c.*360C>T	ENSP00000424113.1:n.*360C>T
ENST00000484444.6:c.*372C>T	ENSP00000420975.1:n.*372C>T
ENST00000488877.6:c.822C>T	ENSP00000425159.1:n.822C>T
ENST00000492756.7:c.*360C>T	ENSP00000422453.1:n.*360C>T
ENST00000494799.6:c.214C>T	ENSP00000512834.1:p.Gln72Ter
ENST00000562983.3:c.214C>T	ENSP00000512845.1:p.Gln72Ter
ENST00000612663.6:c.*333C>T	ENSP00000477997.3:n.*333C>T
ENST00000640140.2:n.1076C>T
ENST00000640250.2:n.430C>T
ENST00000640681.2:n.1035C>T
ENST00000696723.1:n.4564C>T
ENST00000696741.1:n.2569C>T
ENST00000696742.1:n.2296C>T
ENST00000696743.1:n.3699C>T
ENST00000696744.1:n.970C>T
ENST00000696767.1:n.1265C>T
ENST00000696768.1:c.*254C>T	ENSP00000512859.1:n.*254C>T
ENST00000696769.1:n.2620C>T
ENST00000696771.1:c.214C>T	ENSP00000512860.1:p.Gln72Ter
ENST00000696772.1:n.2534C>T
ENST00000696773.1:n.2273C>T
ENST00000696774.1:n.6041C>T
ENST00000696776.1:c.1024C>T	ENSP00000512861.1:p.Gln342Ter
ENST00000696777.1:n.2339C>T
ENST00000696778.1:n.1367C>T
ENST00000696779.1:c.538C>T	ENSP00000512862.1:p.Gln180Ter
ENST00000696780.1:c.961C>T	ENSP00000512863.1:p.Gln321Ter
ENST00000696781.1:c.676C>T	ENSP00000512864.1:p.Gln226Ter
ENST00000696782.1:c.*333C>T	ENSP00000512865.1:n.*333C>T
ENST00000696783.1:n.2799C>T
ENST00000696992.1:n.2048C>T
ENST00000696995.1:n.4460C>T
ENST00000696996.1:n.2373C>T
ENST00000696997.1:c.*561C>T	ENSP00000513028.1:n.*561C>T
ENST00000696998.1:n.2185C>T
ENST00000696999.1:c.214C>T	ENSP00000513029.1:p.Gln72Ter
ENST00000697036.1:c.*347C>T	ENSP00000513060.1:n.*347C>T
ENST00000697037.1:n.966C>T
ENST00000697093.1:n.3167C>T
ENST00000697094.1:n.3514C>T
ENST00000697095.1:c.*2132C>T	ENSP00000513104.1:n.*2132C>T
ENST00000697096.1:n.2064C>T
ENST00000697097.1:c.214C>T	ENSP00000513105.1:p.Gln72Ter
ENST00000562983.2:n.1117C>T
ENST00000690268.1:c.1012C>T	ENSP00000509810.1:p.Gln338Ter
ENST00000355740.7:c.*257C>T	ENSP00000347979.3:n.*257C>T
ENST00000612663.5:c.*333C>T	ENSP00000477997.3:n.*333C>T
ENST00000640140.1:n.1103C>T
ENST00000640250.1:n.430C>T
ENST00000640681.1:n.1052C>T
ENST00000652046.1:c.931C>T MANE Select	ENSP00000498466.1:p.Gln311Ter
ENST00000352159.8:c.*248C>T	ENSP00000345601.4:n.*248C>T
ENST00000355279.2:c.906C>T	ENSP00000347426.2:n.906C>T
ENST00000355740.6:c.931C>T	ENSP00000347979.2:p.Gln311Ter
ENST00000357339.6:c.868C>T	ENSP00000349896.2:p.Gln290Ter
ENST00000479522.5:c.*360C>T	ENSP00000424113.1:n.*360C>T
ENST00000484444.5:c.*372C>T	ENSP00000420975.1:n.*372C>T
ENST00000488877.5:c.*372C>T	ENSP00000425159.1:n.*372C>T
ENST00000492756.5:c.759C>T	ENSP00000422453.1:n.759C>T
ENST00000494410.5:c.*289C>T	ENSP00000423755.1:n.*289C>T
ENST00000612663.4:c.*278C>T	ENSP00000477997.2:n.*278C>T
NM_000043.4:c.931C>T , LRG_134t1:c.931C>T	NP_000034.1:p.Gln311Ter
NM_152871.2:c.868C>T	NP_690610.1:p.Gln290Ter
NM_152872.2:c.*243C>T	NP_690611.1:n.*243C>T
NR_028033.2:n.1105C>T
NR_028034.2:n.967C>T
NR_028035.2:n.1030C>T
NR_028036.2:n.1168C>T
XM_006717819.2:c.1012C>T	XP_006717882.1:p.Gln338Ter
XM_011539764.1:c.1093C>T	XP_011538066.1:p.Gln365Ter
XM_011539765.1:c.1030C>T	XP_011538067.1:p.Gln344Ter
XM_011539766.1:c.1012C>T	XP_011538068.1:p.Gln338Ter
XM_011539767.1:c.976C>T	XP_011538069.1:p.Gln326Ter
XR_945733.1:n.936C>T
NM_000043.5:c.931C>T	NP_000034.1:p.Gln311Ter
NM_001320619.1:c.*254C>T	NP_001307548.1:n.*254C>T
NM_152871.3:c.868C>T	NP_690610.1:p.Gln290Ter
NM_152872.3:c.*243C>T	NP_690611.1:n.*243C>T
NR_028033.3:n.1077C>T
NR_028034.3:n.939C>T
NR_028035.3:n.1002C>T
NR_028036.3:n.1140C>T
NR_135313.1:n.1057C>T
NR_135314.1:n.1240C>T
NR_135315.1:n.993C>T
XM_006717819.3:c.1012C>T	XP_006717882.1:p.Gln338Ter
XM_011539764.2:c.1093C>T	XP_011538066.1:p.Gln365Ter
XM_011539765.2:c.1030C>T	XP_011538067.1:p.Gln344Ter
XM_011539766.2:c.1012C>T	XP_011538068.1:p.Gln338Ter
XM_011539767.3:c.976C>T	XP_011538069.1:p.Gln326Ter
XR_945732.3:n.999C>T
XR_945733.2:n.936C>T
NM_000043.6:c.931C>T MANE Select	NP_000034.1:p.Gln311Ter
NM_001320619.2:c.*254C>T	NP_001307548.1:n.*254C>T
NM_152871.4:c.868C>T	NP_690610.1:p.Gln290Ter
NM_152872.4:c.*243C>T	NP_690611.1:n.*243C>T
NR_028033.4:n.838C>T
NR_028034.4:n.700C>T
NR_028035.4:n.763C>T
NR_028036.4:n.901C>T
NR_135313.2:n.818C>T
NR_135314.2:n.1097C>T
NR_135315.2:n.850C>T