Canonical Allele Identifier: CA377509601

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773905A>G (hg19) ; chr10:g.89014148A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014148A>G , CM000672.2:g.89014148A>G	GRCh38
NC_000010.10:g.90773905A>G , CM000672.1:g.90773905A>G	GRCh37
NC_000010.9:g.90763885A>G	NCBI36
NG_009089.2:g.28618A>G , LRG_134:g.28618A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1015A>G
ENST00000355740.8:c.*29A>G	ENSP00000347979.3:n.*29A>G
ENST00000357339.7:c.643A>G	ENSP00000349896.2:p.Ile215Val
ENST00000371857.8:n.2251A>G
ENST00000460510.6:c.-12A>G	ENSP00000512812.1:n.-12A>G
ENST00000466081.6:n.2355A>G
ENST00000477270.6:c.751A>G	ENSP00000512813.1:p.Ile251Val
ENST00000479522.6:c.*135A>G	ENSP00000424113.1:n.*135A>G
ENST00000484444.6:c.*147A>G	ENSP00000420975.1:n.*147A>G
ENST00000488877.6:c.597A>G	ENSP00000425159.1:n.597A>G
ENST00000492756.7:c.*135A>G	ENSP00000422453.1:n.*135A>G
ENST00000494799.6:c.-12A>G	ENSP00000512834.1:n.-12A>G
ENST00000562983.3:c.-12A>G	ENSP00000512845.1:n.-12A>G
ENST00000612663.6:c.*108A>G	ENSP00000477997.3:n.*108A>G
ENST00000640140.2:n.851A>G
ENST00000640250.2:n.205A>G
ENST00000640681.2:n.810A>G
ENST00000696723.1:n.4339A>G
ENST00000696741.1:n.2344A>G
ENST00000696742.1:n.2071A>G
ENST00000696743.1:n.3474A>G
ENST00000696744.1:n.745A>G
ENST00000696767.1:n.1040A>G
ENST00000696768.1:c.*29A>G	ENSP00000512859.1:n.*29A>G
ENST00000696769.1:n.2395A>G
ENST00000696771.1:c.-12A>G	ENSP00000512860.1:n.-12A>G
ENST00000696772.1:n.2309A>G
ENST00000696773.1:n.2048A>G
ENST00000696774.1:n.5816A>G
ENST00000696776.1:c.799A>G	ENSP00000512861.1:p.Ile267Val
ENST00000696777.1:n.2114A>G
ENST00000696778.1:n.1142A>G
ENST00000696779.1:c.313A>G	ENSP00000512862.1:p.Ile105Val
ENST00000696780.1:c.736A>G	ENSP00000512863.1:p.Ile246Val
ENST00000696781.1:c.451A>G	ENSP00000512864.1:p.Ile151Val
ENST00000696782.1:c.*108A>G	ENSP00000512865.1:n.*108A>G
ENST00000696783.1:n.2574A>G
ENST00000696992.1:n.1823A>G
ENST00000696995.1:n.4235A>G
ENST00000696996.1:n.2148A>G
ENST00000696997.1:c.*336A>G	ENSP00000513028.1:n.*336A>G
ENST00000696998.1:n.1960A>G
ENST00000696999.1:c.-12A>G	ENSP00000513029.1:n.-12A>G
ENST00000697035.1:c.*39A>G	ENSP00000513059.1:n.*39A>G
ENST00000697036.1:c.*122A>G	ENSP00000513060.1:n.*122A>G
ENST00000697037.1:n.741A>G
ENST00000697093.1:n.2942A>G
ENST00000697094.1:n.3289A>G
ENST00000697095.1:c.*1907A>G	ENSP00000513104.1:n.*1907A>G
ENST00000697096.1:n.1839A>G
ENST00000697097.1:c.-12A>G	ENSP00000513105.1:n.-12A>G
ENST00000562983.2:n.892A>G
ENST00000690268.1:c.787A>G	ENSP00000509810.1:p.Ile263Val
ENST00000355740.7:c.*32A>G	ENSP00000347979.3:n.*32A>G
ENST00000612663.5:c.*108A>G	ENSP00000477997.3:n.*108A>G
ENST00000640140.1:n.878A>G
ENST00000640250.1:n.205A>G
ENST00000640681.1:n.827A>G
ENST00000652046.1:c.706A>G MANE Select	ENSP00000498466.1:p.Ile236Val
ENST00000313771.9:n.1015A>G
ENST00000352159.8:c.*23A>G	ENSP00000345601.4:n.*23A>G
ENST00000355279.2:c.681A>G	ENSP00000347426.2:n.681A>G
ENST00000355740.6:c.706A>G	ENSP00000347979.2:p.Ile236Val
ENST00000357339.6:c.643A>G	ENSP00000349896.2:p.Ile215Val
ENST00000479522.5:c.*135A>G	ENSP00000424113.1:n.*135A>G
ENST00000484444.5:c.*147A>G	ENSP00000420975.1:n.*147A>G
ENST00000488877.5:c.*147A>G	ENSP00000425159.1:n.*147A>G
ENST00000492756.5:c.534A>G	ENSP00000422453.1:n.534A>G
ENST00000494410.5:c.*64A>G	ENSP00000423755.1:n.*64A>G
ENST00000494799.5:n.613A>G
ENST00000612663.4:c.*53A>G	ENSP00000477997.2:n.*53A>G
ENST00000615406.4:c.706A>G	ENSP00000484575.1:p.Ile236Val
ENST00000626542.2:c.704A>G	ENSP00000485876.1:p.Tyr235Cys
NM_000043.4:c.706A>G , LRG_134t1:c.706A>G	NP_000034.1:p.Ile236Val
NM_152871.2:c.643A>G	NP_690610.1:p.Ile215Val
NM_152872.2:c.*18A>G	NP_690611.1:n.*18A>G
NR_028033.2:n.880A>G
NR_028034.2:n.742A>G
NR_028035.2:n.805A>G
NR_028036.2:n.943A>G
XM_006717819.2:c.787A>G	XP_006717882.1:p.Ile263Val
XM_011539764.1:c.868A>G	XP_011538066.1:p.Ile290Val
XM_011539765.1:c.805A>G	XP_011538067.1:p.Ile269Val
XM_011539766.1:c.787A>G	XP_011538068.1:p.Ile263Val
XM_011539767.1:c.751A>G	XP_011538069.1:p.Ile251Val
XR_945732.1:n.774A>G
XR_945733.1:n.711A>G
NM_000043.5:c.706A>G	NP_000034.1:p.Ile236Val
NM_001320619.1:c.*29A>G	NP_001307548.1:n.*29A>G
NM_152871.3:c.643A>G	NP_690610.1:p.Ile215Val
NM_152872.3:c.*18A>G	NP_690611.1:n.*18A>G
NR_028033.3:n.852A>G
NR_028034.3:n.714A>G
NR_028035.3:n.777A>G
NR_028036.3:n.915A>G
NR_135313.1:n.832A>G
NR_135314.1:n.1015A>G
NR_135315.1:n.768A>G
XM_006717819.3:c.787A>G	XP_006717882.1:p.Ile263Val
XM_011539764.2:c.868A>G	XP_011538066.1:p.Ile290Val
XM_011539765.2:c.805A>G	XP_011538067.1:p.Ile269Val
XM_011539766.2:c.787A>G	XP_011538068.1:p.Ile263Val
XM_011539767.3:c.751A>G	XP_011538069.1:p.Ile251Val
XR_945732.3:n.774A>G
XR_945733.2:n.711A>G
NM_000043.6:c.706A>G MANE Select	NP_000034.1:p.Ile236Val
NM_001320619.2:c.*29A>G	NP_001307548.1:n.*29A>G
NM_152871.4:c.643A>G	NP_690610.1:p.Ile215Val
NM_152872.4:c.*18A>G	NP_690611.1:n.*18A>G
NR_028033.4:n.613A>G
NR_028034.4:n.475A>G
NR_028035.4:n.538A>G
NR_028036.4:n.676A>G
NR_135313.2:n.593A>G
NR_135314.2:n.872A>G
NR_135315.2:n.625A>G