Canonical Allele Identifier: CA5593231

Gene: FAS

Linked Data

• dbSNP Id: rs754300614
• ExAC: 10:90774076 A / G
• gnomAD v2: 10-90774076-A-G
• gnomAD v4: 10-89014319-A-G
• MyVariant Identifiers: chr10:g.90774076A>G (hg19) ; chr10:g.89014319A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014319A>G , CM000672.2:g.89014319A>G	GRCh38
NC_000010.10:g.90774076A>G , CM000672.1:g.90774076A>G	GRCh37
NC_000010.9:g.90764056A>G	NCBI36
NG_009089.2:g.28789A>G , LRG_134:g.28789A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1186A>G
ENST00000355740.8:c.*200A>G	ENSP00000347979.3:n.*200A>G
ENST00000357339.7:c.814A>G	ENSP00000349896.2:p.Thr272Ala
ENST00000371857.8:n.2422A>G
ENST00000460510.6:c.160A>G	ENSP00000512812.1:p.Thr54Ala
ENST00000466081.6:n.2526A>G
ENST00000477270.6:c.922A>G	ENSP00000512813.1:p.Thr308Ala
ENST00000479522.6:c.*306A>G	ENSP00000424113.1:n.*306A>G
ENST00000484444.6:c.*318A>G	ENSP00000420975.1:n.*318A>G
ENST00000488877.6:c.768A>G	ENSP00000425159.1:n.768A>G
ENST00000492756.7:c.*306A>G	ENSP00000422453.1:n.*306A>G
ENST00000494799.6:c.160A>G	ENSP00000512834.1:p.Thr54Ala
ENST00000562983.3:c.160A>G	ENSP00000512845.1:p.Thr54Ala
ENST00000612663.6:c.*279A>G	ENSP00000477997.3:n.*279A>G
ENST00000640140.2:n.1022A>G
ENST00000640250.2:n.376A>G
ENST00000640681.2:n.981A>G
ENST00000696723.1:n.4510A>G
ENST00000696741.1:n.2515A>G
ENST00000696742.1:n.2242A>G
ENST00000696743.1:n.3645A>G
ENST00000696744.1:n.916A>G
ENST00000696767.1:n.1211A>G
ENST00000696768.1:c.*200A>G	ENSP00000512859.1:n.*200A>G
ENST00000696769.1:n.2566A>G
ENST00000696771.1:c.160A>G	ENSP00000512860.1:p.Thr54Ala
ENST00000696772.1:n.2480A>G
ENST00000696773.1:n.2219A>G
ENST00000696774.1:n.5987A>G
ENST00000696776.1:c.970A>G	ENSP00000512861.1:p.Thr324Ala
ENST00000696777.1:n.2285A>G
ENST00000696778.1:n.1313A>G
ENST00000696779.1:c.484A>G	ENSP00000512862.1:p.Thr162Ala
ENST00000696780.1:c.907A>G	ENSP00000512863.1:p.Thr303Ala
ENST00000696781.1:c.622A>G	ENSP00000512864.1:p.Thr208Ala
ENST00000696782.1:c.*279A>G	ENSP00000512865.1:n.*279A>G
ENST00000696783.1:n.2745A>G
ENST00000696992.1:n.1994A>G
ENST00000696995.1:n.4406A>G
ENST00000696996.1:n.2319A>G
ENST00000696997.1:c.*507A>G	ENSP00000513028.1:n.*507A>G
ENST00000696998.1:n.2131A>G
ENST00000696999.1:c.160A>G	ENSP00000513029.1:p.Thr54Ala
ENST00000697036.1:c.*293A>G	ENSP00000513060.1:n.*293A>G
ENST00000697037.1:n.912A>G
ENST00000697093.1:n.3113A>G
ENST00000697094.1:n.3460A>G
ENST00000697095.1:c.*2078A>G	ENSP00000513104.1:n.*2078A>G
ENST00000697096.1:n.2010A>G
ENST00000697097.1:c.160A>G	ENSP00000513105.1:p.Thr54Ala
ENST00000562983.2:n.1063A>G
ENST00000690268.1:c.958A>G	ENSP00000509810.1:p.Thr320Ala
ENST00000355740.7:c.*203A>G	ENSP00000347979.3:n.*203A>G
ENST00000612663.5:c.*279A>G	ENSP00000477997.3:n.*279A>G
ENST00000640140.1:n.1049A>G
ENST00000640250.1:n.376A>G
ENST00000640681.1:n.998A>G
ENST00000652046.1:c.877A>G MANE Select	ENSP00000498466.1:p.Thr293Ala
ENST00000352159.8:c.*194A>G	ENSP00000345601.4:n.*194A>G
ENST00000355279.2:c.852A>G	ENSP00000347426.2:n.852A>G
ENST00000355740.6:c.877A>G	ENSP00000347979.2:p.Thr293Ala
ENST00000357339.6:c.814A>G	ENSP00000349896.2:p.Thr272Ala
ENST00000479522.5:c.*306A>G	ENSP00000424113.1:n.*306A>G
ENST00000484444.5:c.*318A>G	ENSP00000420975.1:n.*318A>G
ENST00000488877.5:c.*318A>G	ENSP00000425159.1:n.*318A>G
ENST00000492756.5:c.705A>G	ENSP00000422453.1:n.705A>G
ENST00000494410.5:c.*235A>G	ENSP00000423755.1:n.*235A>G
ENST00000612663.4:c.*224A>G	ENSP00000477997.2:n.*224A>G
NM_000043.4:c.877A>G , LRG_134t1:c.877A>G	NP_000034.1:p.Thr293Ala
NM_152871.2:c.814A>G	NP_690610.1:p.Thr272Ala
NM_152872.2:c.*189A>G	NP_690611.1:n.*189A>G
NR_028033.2:n.1051A>G
NR_028034.2:n.913A>G
NR_028035.2:n.976A>G
NR_028036.2:n.1114A>G
XM_006717819.2:c.958A>G	XP_006717882.1:p.Thr320Ala
XM_011539764.1:c.1039A>G	XP_011538066.1:p.Thr347Ala
XM_011539765.1:c.976A>G	XP_011538067.1:p.Thr326Ala
XM_011539766.1:c.958A>G	XP_011538068.1:p.Thr320Ala
XM_011539767.1:c.922A>G	XP_011538069.1:p.Thr308Ala
XR_945732.1:n.945A>G
XR_945733.1:n.882A>G
NM_000043.5:c.877A>G	NP_000034.1:p.Thr293Ala
NM_001320619.1:c.*200A>G	NP_001307548.1:n.*200A>G
NM_152871.3:c.814A>G	NP_690610.1:p.Thr272Ala
NM_152872.3:c.*189A>G	NP_690611.1:n.*189A>G
NR_028033.3:n.1023A>G
NR_028034.3:n.885A>G
NR_028035.3:n.948A>G
NR_028036.3:n.1086A>G
NR_135313.1:n.1003A>G
NR_135314.1:n.1186A>G
NR_135315.1:n.939A>G
XM_006717819.3:c.958A>G	XP_006717882.1:p.Thr320Ala
XM_011539764.2:c.1039A>G	XP_011538066.1:p.Thr347Ala
XM_011539765.2:c.976A>G	XP_011538067.1:p.Thr326Ala
XM_011539766.2:c.958A>G	XP_011538068.1:p.Thr320Ala
XM_011539767.3:c.922A>G	XP_011538069.1:p.Thr308Ala
XR_945732.3:n.945A>G
XR_945733.2:n.882A>G
NM_000043.6:c.877A>G MANE Select	NP_000034.1:p.Thr293Ala
NM_001320619.2:c.*200A>G	NP_001307548.1:n.*200A>G
NM_152871.4:c.814A>G	NP_690610.1:p.Thr272Ala
NM_152872.4:c.*189A>G	NP_690611.1:n.*189A>G
NR_028033.4:n.784A>G
NR_028034.4:n.646A>G
NR_028035.4:n.709A>G
NR_028036.4:n.847A>G
NR_135313.2:n.764A>G
NR_135314.2:n.1043A>G
NR_135315.2:n.796A>G