Canonical Allele Identifier: CA377510104

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774115C>T (hg19) ; chr10:g.89014358C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014358C>T , CM000672.2:g.89014358C>T	GRCh38
NC_000010.10:g.90774115C>T , CM000672.1:g.90774115C>T	GRCh37
NC_000010.9:g.90764095C>T	NCBI36
NG_009089.2:g.28828C>T , LRG_134:g.28828C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1225C>T
ENST00000355740.8:c.*239C>T	ENSP00000347979.3:n.*239C>T
ENST00000357339.7:c.853C>T	ENSP00000349896.2:p.Leu285Phe
ENST00000371857.8:n.2461C>T
ENST00000460510.6:c.199C>T	ENSP00000512812.1:p.Leu67Phe
ENST00000466081.6:n.2565C>T
ENST00000477270.6:c.961C>T	ENSP00000512813.1:p.Leu321Phe
ENST00000479522.6:c.*345C>T	ENSP00000424113.1:n.*345C>T
ENST00000484444.6:c.*357C>T	ENSP00000420975.1:n.*357C>T
ENST00000488877.6:c.807C>T	ENSP00000425159.1:n.807C>T
ENST00000492756.7:c.*345C>T	ENSP00000422453.1:n.*345C>T
ENST00000494799.6:c.199C>T	ENSP00000512834.1:p.Leu67Phe
ENST00000562983.3:c.199C>T	ENSP00000512845.1:p.Leu67Phe
ENST00000612663.6:c.*318C>T	ENSP00000477997.3:n.*318C>T
ENST00000640140.2:n.1061C>T
ENST00000640250.2:n.415C>T
ENST00000640681.2:n.1020C>T
ENST00000696723.1:n.4549C>T
ENST00000696741.1:n.2554C>T
ENST00000696742.1:n.2281C>T
ENST00000696743.1:n.3684C>T
ENST00000696744.1:n.955C>T
ENST00000696767.1:n.1250C>T
ENST00000696768.1:c.*239C>T	ENSP00000512859.1:n.*239C>T
ENST00000696769.1:n.2605C>T
ENST00000696771.1:c.199C>T	ENSP00000512860.1:p.Leu67Phe
ENST00000696772.1:n.2519C>T
ENST00000696773.1:n.2258C>T
ENST00000696774.1:n.6026C>T
ENST00000696776.1:c.1009C>T	ENSP00000512861.1:p.Leu337Phe
ENST00000696777.1:n.2324C>T
ENST00000696778.1:n.1352C>T
ENST00000696779.1:c.523C>T	ENSP00000512862.1:p.Leu175Phe
ENST00000696780.1:c.946C>T	ENSP00000512863.1:p.Leu316Phe
ENST00000696781.1:c.661C>T	ENSP00000512864.1:p.Leu221Phe
ENST00000696782.1:c.*318C>T	ENSP00000512865.1:n.*318C>T
ENST00000696783.1:n.2784C>T
ENST00000696992.1:n.2033C>T
ENST00000696995.1:n.4445C>T
ENST00000696996.1:n.2358C>T
ENST00000696997.1:c.*546C>T	ENSP00000513028.1:n.*546C>T
ENST00000696998.1:n.2170C>T
ENST00000696999.1:c.199C>T	ENSP00000513029.1:p.Leu67Phe
ENST00000697036.1:c.*332C>T	ENSP00000513060.1:n.*332C>T
ENST00000697037.1:n.951C>T
ENST00000697093.1:n.3152C>T
ENST00000697094.1:n.3499C>T
ENST00000697095.1:c.*2117C>T	ENSP00000513104.1:n.*2117C>T
ENST00000697096.1:n.2049C>T
ENST00000697097.1:c.199C>T	ENSP00000513105.1:p.Leu67Phe
ENST00000562983.2:n.1102C>T
ENST00000690268.1:c.997C>T	ENSP00000509810.1:p.Leu333Phe
ENST00000355740.7:c.*242C>T	ENSP00000347979.3:n.*242C>T
ENST00000612663.5:c.*318C>T	ENSP00000477997.3:n.*318C>T
ENST00000640140.1:n.1088C>T
ENST00000640250.1:n.415C>T
ENST00000640681.1:n.1037C>T
ENST00000652046.1:c.916C>T MANE Select	ENSP00000498466.1:p.Leu306Phe
ENST00000352159.8:c.*233C>T	ENSP00000345601.4:n.*233C>T
ENST00000355279.2:c.891C>T	ENSP00000347426.2:n.891C>T
ENST00000355740.6:c.916C>T	ENSP00000347979.2:p.Leu306Phe
ENST00000357339.6:c.853C>T	ENSP00000349896.2:p.Leu285Phe
ENST00000479522.5:c.*345C>T	ENSP00000424113.1:n.*345C>T
ENST00000484444.5:c.*357C>T	ENSP00000420975.1:n.*357C>T
ENST00000488877.5:c.*357C>T	ENSP00000425159.1:n.*357C>T
ENST00000492756.5:c.744C>T	ENSP00000422453.1:n.744C>T
ENST00000494410.5:c.*274C>T	ENSP00000423755.1:n.*274C>T
ENST00000612663.4:c.*263C>T	ENSP00000477997.2:n.*263C>T
NM_000043.4:c.916C>T , LRG_134t1:c.916C>T	NP_000034.1:p.Leu306Phe
NM_152871.2:c.853C>T	NP_690610.1:p.Leu285Phe
NM_152872.2:c.*228C>T	NP_690611.1:n.*228C>T
NR_028033.2:n.1090C>T
NR_028034.2:n.952C>T
NR_028035.2:n.1015C>T
NR_028036.2:n.1153C>T
XM_006717819.2:c.997C>T	XP_006717882.1:p.Leu333Phe
XM_011539764.1:c.1078C>T	XP_011538066.1:p.Leu360Phe
XM_011539765.1:c.1015C>T	XP_011538067.1:p.Leu339Phe
XM_011539766.1:c.997C>T	XP_011538068.1:p.Leu333Phe
XM_011539767.1:c.961C>T	XP_011538069.1:p.Leu321Phe
XR_945732.1:n.984C>T
XR_945733.1:n.921C>T
NM_000043.5:c.916C>T	NP_000034.1:p.Leu306Phe
NM_001320619.1:c.*239C>T	NP_001307548.1:n.*239C>T
NM_152871.3:c.853C>T	NP_690610.1:p.Leu285Phe
NM_152872.3:c.*228C>T	NP_690611.1:n.*228C>T
NR_028033.3:n.1062C>T
NR_028034.3:n.924C>T
NR_028035.3:n.987C>T
NR_028036.3:n.1125C>T
NR_135313.1:n.1042C>T
NR_135314.1:n.1225C>T
NR_135315.1:n.978C>T
XM_006717819.3:c.997C>T	XP_006717882.1:p.Leu333Phe
XM_011539764.2:c.1078C>T	XP_011538066.1:p.Leu360Phe
XM_011539765.2:c.1015C>T	XP_011538067.1:p.Leu339Phe
XM_011539766.2:c.997C>T	XP_011538068.1:p.Leu333Phe
XM_011539767.3:c.961C>T	XP_011538069.1:p.Leu321Phe
XR_945732.3:n.984C>T
XR_945733.2:n.921C>T
NM_000043.6:c.916C>T MANE Select	NP_000034.1:p.Leu306Phe
NM_001320619.2:c.*239C>T	NP_001307548.1:n.*239C>T
NM_152871.4:c.853C>T	NP_690610.1:p.Leu285Phe
NM_152872.4:c.*228C>T	NP_690611.1:n.*228C>T
NR_028033.4:n.823C>T
NR_028034.4:n.685C>T
NR_028035.4:n.748C>T
NR_028036.4:n.886C>T
NR_135313.2:n.803C>T
NR_135314.2:n.1082C>T
NR_135315.2:n.835C>T