Canonical Allele Identifier: CA891843083

Gene: FAS

Linked Data

• ClinVar Variation Id: 578533
• ClinVar RCV Id: RCV000701568
• dbSNP Id: rs1564699214
• MyVariant Identifiers: chr10:g.90773954del (hg19) ; chr10:g.89014197del (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1064del
ENST00000355740.8:c.*78del	ENSP00000347979.3:n.*78del
ENST00000357339.7:c.692del	ENSP00000349896.2:p.Asn231MetfsTer8
ENST00000371857.8:n.2300del
ENST00000460510.6:c.38del	ENSP00000512812.1:p.Asn13MetfsTer8
ENST00000466081.6:n.2404del
ENST00000477270.6:c.800del	ENSP00000512813.1:p.Asn267MetfsTer8
ENST00000479522.6:c.*184del	ENSP00000424113.1:n.*184del
ENST00000484444.6:c.*196del	ENSP00000420975.1:n.*196del
ENST00000488877.6:c.646del	ENSP00000425159.1:n.646del
ENST00000492756.7:c.*184del	ENSP00000422453.1:n.*184del
ENST00000494799.6:c.38del	ENSP00000512834.1:p.Asn13MetfsTer8
ENST00000562983.3:c.38del	ENSP00000512845.1:p.Asn13MetfsTer8
ENST00000612663.6:c.*157del	ENSP00000477997.3:n.*157del
ENST00000640140.2:n.900del
ENST00000640250.2:n.254del
ENST00000640681.2:n.859del
ENST00000696723.1:n.4388del
ENST00000696741.1:n.2393del
ENST00000696742.1:n.2120del
ENST00000696743.1:n.3523del
ENST00000696744.1:n.794del
ENST00000696767.1:n.1089del
ENST00000696768.1:c.*78del	ENSP00000512859.1:n.*78del
ENST00000696769.1:n.2444del
ENST00000696771.1:c.38del	ENSP00000512860.1:p.Asn13MetfsTer8
ENST00000696772.1:n.2358del
ENST00000696773.1:n.2097del
ENST00000696774.1:n.5865del
ENST00000696776.1:c.848del	ENSP00000512861.1:p.Asn283MetfsTer8
ENST00000696777.1:n.2163del
ENST00000696778.1:n.1191del
ENST00000696779.1:c.362del	ENSP00000512862.1:p.Asn121MetfsTer8
ENST00000696780.1:c.785del	ENSP00000512863.1:p.Asn262MetfsTer8
ENST00000696781.1:c.500del	ENSP00000512864.1:p.Asn167MetfsTer8
ENST00000696782.1:c.*157del	ENSP00000512865.1:n.*157del
ENST00000696783.1:n.2623del
ENST00000696992.1:n.1872del
ENST00000696995.1:n.4284del
ENST00000696996.1:n.2197del
ENST00000696997.1:c.*385del	ENSP00000513028.1:n.*385del
ENST00000696998.1:n.2009del
ENST00000696999.1:c.38del	ENSP00000513029.1:p.Asn13MetfsTer8
ENST00000697035.1:c.*88del	ENSP00000513059.1:n.*88del
ENST00000697036.1:c.*171del	ENSP00000513060.1:n.*171del
ENST00000697037.1:n.790del
ENST00000697093.1:n.2991del
ENST00000697094.1:n.3338del
ENST00000697095.1:c.*1956del	ENSP00000513104.1:n.*1956del
ENST00000697096.1:n.1888del
ENST00000697097.1:c.38del	ENSP00000513105.1:p.Asn13MetfsTer8
ENST00000562983.2:n.941del
ENST00000690268.1:c.836del	ENSP00000509810.1:p.Asn279MetfsTer8
ENST00000355740.7:c.*81del	ENSP00000347979.3:n.*81del
ENST00000612663.5:c.*157del	ENSP00000477997.3:n.*157del
ENST00000640140.1:n.927del
ENST00000640250.1:n.254del
ENST00000640681.1:n.876del
ENST00000652046.1:c.755del MANE Select	ENSP00000498466.1:p.Asn252MetfsTer8
ENST00000352159.8:c.*72del	ENSP00000345601.4:n.*72del
ENST00000355279.2:c.730del	ENSP00000347426.2:n.730del
ENST00000355740.6:c.755del	ENSP00000347979.2:p.Asn252MetfsTer8
ENST00000357339.6:c.692del	ENSP00000349896.2:p.Asn231MetfsTer8
ENST00000479522.5:c.*184del	ENSP00000424113.1:n.*184del
ENST00000484444.5:c.*196del	ENSP00000420975.1:n.*196del
ENST00000488877.5:c.*196del	ENSP00000425159.1:n.*196del
ENST00000492756.5:c.583del	ENSP00000422453.1:n.583del
ENST00000494410.5:c.*113del	ENSP00000423755.1:n.*113del
ENST00000494799.5:n.662del
ENST00000612663.4:c.*102del	ENSP00000477997.2:n.*102del
ENST00000615406.4:c.753del	ENSP00000484575.1:p.Glu251AspfsTer?
NM_000043.4:c.755del , LRG_134t1:c.755del	NP_000034.1:p.Asn252MetfsTer8
NM_152871.2:c.692del	NP_690610.1:p.Asn231MetfsTer8
NM_152872.2:c.*67del	NP_690611.1:n.*67del
NR_028033.2:n.929del
NR_028034.2:n.791del
NR_028035.2:n.854del
NR_028036.2:n.992del
XM_006717819.2:c.836del	XP_006717882.1:p.Asn279MetfsTer8
XM_011539764.1:c.917del	XP_011538066.1:p.Asn306MetfsTer8
XM_011539765.1:c.854del	XP_011538067.1:p.Asn285MetfsTer8
XM_011539766.1:c.836del	XP_011538068.1:p.Asn279MetfsTer8
XM_011539767.1:c.800del	XP_011538069.1:p.Asn267MetfsTer8
XR_945732.1:n.823del
XR_945733.1:n.760del
NM_000043.5:c.755del	NP_000034.1:p.Asn252MetfsTer8
NM_001320619.1:c.*78del	NP_001307548.1:n.*78del
NM_152871.3:c.692del	NP_690610.1:p.Asn231MetfsTer8
NM_152872.3:c.*67del	NP_690611.1:n.*67del
NR_028033.3:n.901del
NR_028034.3:n.763del
NR_028035.3:n.826del
NR_028036.3:n.964del
NR_135313.1:n.881del
NR_135314.1:n.1064del
NR_135315.1:n.817del
XM_006717819.3:c.836del	XP_006717882.1:p.Asn279MetfsTer8
XM_011539764.2:c.917del	XP_011538066.1:p.Asn306MetfsTer8
XM_011539765.2:c.854del	XP_011538067.1:p.Asn285MetfsTer8
XM_011539766.2:c.836del	XP_011538068.1:p.Asn279MetfsTer8
XM_011539767.3:c.800del	XP_011538069.1:p.Asn267MetfsTer8
XR_945732.3:n.823del
XR_945733.2:n.760del
NM_000043.6:c.755del MANE Select	NP_000034.1:p.Asn252MetfsTer8
NM_001320619.2:c.*78del	NP_001307548.1:n.*78del
NM_152871.4:c.692del	NP_690610.1:p.Asn231MetfsTer8
NM_152872.4:c.*67del	NP_690611.1:n.*67del
NR_028033.4:n.662del
NR_028034.4:n.524del
NR_028035.4:n.587del
NR_028036.4:n.725del
NR_135313.2:n.642del
NR_135314.2:n.921del
NR_135315.2:n.674del