Canonical Allele Identifier: CA377509724

Gene: FAS

Linked Data

• gnomAD v4: 10-89014197-A-G
• MyVariant Identifiers: chr10:g.90773954A>G (hg19) ; chr10:g.89014197A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014197A>G , CM000672.2:g.89014197A>G	GRCh38
NC_000010.10:g.90773954A>G , CM000672.1:g.90773954A>G	GRCh37
NC_000010.9:g.90763934A>G	NCBI36
NG_009089.2:g.28667A>G , LRG_134:g.28667A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1064A>G
ENST00000355740.8:c.*78A>G	ENSP00000347979.3:n.*78A>G
ENST00000357339.7:c.692A>G	ENSP00000349896.2:p.Asn231Ser
ENST00000371857.8:n.2300A>G
ENST00000460510.6:c.38A>G	ENSP00000512812.1:p.Asn13Ser
ENST00000466081.6:n.2404A>G
ENST00000477270.6:c.800A>G	ENSP00000512813.1:p.Asn267Ser
ENST00000479522.6:c.*184A>G	ENSP00000424113.1:n.*184A>G
ENST00000484444.6:c.*196A>G	ENSP00000420975.1:n.*196A>G
ENST00000488877.6:c.646A>G	ENSP00000425159.1:n.646A>G
ENST00000492756.7:c.*184A>G	ENSP00000422453.1:n.*184A>G
ENST00000494799.6:c.38A>G	ENSP00000512834.1:p.Asn13Ser
ENST00000562983.3:c.38A>G	ENSP00000512845.1:p.Asn13Ser
ENST00000612663.6:c.*157A>G	ENSP00000477997.3:n.*157A>G
ENST00000640140.2:n.900A>G
ENST00000640250.2:n.254A>G
ENST00000640681.2:n.859A>G
ENST00000696723.1:n.4388A>G
ENST00000696741.1:n.2393A>G
ENST00000696742.1:n.2120A>G
ENST00000696743.1:n.3523A>G
ENST00000696744.1:n.794A>G
ENST00000696767.1:n.1089A>G
ENST00000696768.1:c.*78A>G	ENSP00000512859.1:n.*78A>G
ENST00000696769.1:n.2444A>G
ENST00000696771.1:c.38A>G	ENSP00000512860.1:p.Asn13Ser
ENST00000696772.1:n.2358A>G
ENST00000696773.1:n.2097A>G
ENST00000696774.1:n.5865A>G
ENST00000696776.1:c.848A>G	ENSP00000512861.1:p.Asn283Ser
ENST00000696777.1:n.2163A>G
ENST00000696778.1:n.1191A>G
ENST00000696779.1:c.362A>G	ENSP00000512862.1:p.Asn121Ser
ENST00000696780.1:c.785A>G	ENSP00000512863.1:p.Asn262Ser
ENST00000696781.1:c.500A>G	ENSP00000512864.1:p.Asn167Ser
ENST00000696782.1:c.*157A>G	ENSP00000512865.1:n.*157A>G
ENST00000696783.1:n.2623A>G
ENST00000696992.1:n.1872A>G
ENST00000696995.1:n.4284A>G
ENST00000696996.1:n.2197A>G
ENST00000696997.1:c.*385A>G	ENSP00000513028.1:n.*385A>G
ENST00000696998.1:n.2009A>G
ENST00000696999.1:c.38A>G	ENSP00000513029.1:p.Asn13Ser
ENST00000697035.1:c.*88A>G	ENSP00000513059.1:n.*88A>G
ENST00000697036.1:c.*171A>G	ENSP00000513060.1:n.*171A>G
ENST00000697037.1:n.790A>G
ENST00000697093.1:n.2991A>G
ENST00000697094.1:n.3338A>G
ENST00000697095.1:c.*1956A>G	ENSP00000513104.1:n.*1956A>G
ENST00000697096.1:n.1888A>G
ENST00000697097.1:c.38A>G	ENSP00000513105.1:p.Asn13Ser
ENST00000562983.2:n.941A>G
ENST00000690268.1:c.836A>G	ENSP00000509810.1:p.Asn279Ser
ENST00000355740.7:c.*81A>G	ENSP00000347979.3:n.*81A>G
ENST00000612663.5:c.*157A>G	ENSP00000477997.3:n.*157A>G
ENST00000640140.1:n.927A>G
ENST00000640250.1:n.254A>G
ENST00000640681.1:n.876A>G
ENST00000652046.1:c.755A>G MANE Select	ENSP00000498466.1:p.Asn252Ser
ENST00000352159.8:c.*72A>G	ENSP00000345601.4:n.*72A>G
ENST00000355279.2:c.730A>G	ENSP00000347426.2:n.730A>G
ENST00000355740.6:c.755A>G	ENSP00000347979.2:p.Asn252Ser
ENST00000357339.6:c.692A>G	ENSP00000349896.2:p.Asn231Ser
ENST00000479522.5:c.*184A>G	ENSP00000424113.1:n.*184A>G
ENST00000484444.5:c.*196A>G	ENSP00000420975.1:n.*196A>G
ENST00000488877.5:c.*196A>G	ENSP00000425159.1:n.*196A>G
ENST00000492756.5:c.583A>G	ENSP00000422453.1:n.583A>G
ENST00000494410.5:c.*113A>G	ENSP00000423755.1:n.*113A>G
ENST00000494799.5:n.662A>G
ENST00000612663.4:c.*102A>G	ENSP00000477997.2:n.*102A>G
ENST00000615406.4:c.753A>G	ENSP00000484575.1:p.Glu251=
NM_000043.4:c.755A>G , LRG_134t1:c.755A>G	NP_000034.1:p.Asn252Ser
NM_152871.2:c.692A>G	NP_690610.1:p.Asn231Ser
NM_152872.2:c.*67A>G	NP_690611.1:n.*67A>G
NR_028033.2:n.929A>G
NR_028034.2:n.791A>G
NR_028035.2:n.854A>G
NR_028036.2:n.992A>G
XM_006717819.2:c.836A>G	XP_006717882.1:p.Asn279Ser
XM_011539764.1:c.917A>G	XP_011538066.1:p.Asn306Ser
XM_011539765.1:c.854A>G	XP_011538067.1:p.Asn285Ser
XM_011539766.1:c.836A>G	XP_011538068.1:p.Asn279Ser
XM_011539767.1:c.800A>G	XP_011538069.1:p.Asn267Ser
XR_945732.1:n.823A>G
XR_945733.1:n.760A>G
NM_000043.5:c.755A>G	NP_000034.1:p.Asn252Ser
NM_001320619.1:c.*78A>G	NP_001307548.1:n.*78A>G
NM_152871.3:c.692A>G	NP_690610.1:p.Asn231Ser
NM_152872.3:c.*67A>G	NP_690611.1:n.*67A>G
NR_028033.3:n.901A>G
NR_028034.3:n.763A>G
NR_028035.3:n.826A>G
NR_028036.3:n.964A>G
NR_135313.1:n.881A>G
NR_135314.1:n.1064A>G
NR_135315.1:n.817A>G
XM_006717819.3:c.836A>G	XP_006717882.1:p.Asn279Ser
XM_011539764.2:c.917A>G	XP_011538066.1:p.Asn306Ser
XM_011539765.2:c.854A>G	XP_011538067.1:p.Asn285Ser
XM_011539766.2:c.836A>G	XP_011538068.1:p.Asn279Ser
XM_011539767.3:c.800A>G	XP_011538069.1:p.Asn267Ser
XR_945732.3:n.823A>G
XR_945733.2:n.760A>G
NM_000043.6:c.755A>G MANE Select	NP_000034.1:p.Asn252Ser
NM_001320619.2:c.*78A>G	NP_001307548.1:n.*78A>G
NM_152871.4:c.692A>G	NP_690610.1:p.Asn231Ser
NM_152872.4:c.*67A>G	NP_690611.1:n.*67A>G
NR_028033.4:n.662A>G
NR_028034.4:n.524A>G
NR_028035.4:n.587A>G
NR_028036.4:n.725A>G
NR_135313.2:n.642A>G
NR_135314.2:n.921A>G
NR_135315.2:n.674A>G