Canonical Allele Identifier: CA377509779

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773973A>C (hg19) ; chr10:g.89014216A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014216A>C , CM000672.2:g.89014216A>C	GRCh38
NC_000010.10:g.90773973A>C , CM000672.1:g.90773973A>C	GRCh37
NC_000010.9:g.90763953A>C	NCBI36
NG_009089.2:g.28686A>C , LRG_134:g.28686A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1083A>C
ENST00000355740.8:c.*97A>C	ENSP00000347979.3:n.*97A>C
ENST00000357339.7:c.711A>C	ENSP00000349896.2:p.Lys237Asn
ENST00000371857.8:n.2319A>C
ENST00000460510.6:c.57A>C	ENSP00000512812.1:p.Lys19Asn
ENST00000466081.6:n.2423A>C
ENST00000477270.6:c.819A>C	ENSP00000512813.1:p.Lys273Asn
ENST00000479522.6:c.*203A>C	ENSP00000424113.1:n.*203A>C
ENST00000484444.6:c.*215A>C	ENSP00000420975.1:n.*215A>C
ENST00000488877.6:c.665A>C	ENSP00000425159.1:n.665A>C
ENST00000492756.7:c.*203A>C	ENSP00000422453.1:n.*203A>C
ENST00000494799.6:c.57A>C	ENSP00000512834.1:p.Lys19Asn
ENST00000562983.3:c.57A>C	ENSP00000512845.1:p.Lys19Asn
ENST00000612663.6:c.*176A>C	ENSP00000477997.3:n.*176A>C
ENST00000640140.2:n.919A>C
ENST00000640250.2:n.273A>C
ENST00000640681.2:n.878A>C
ENST00000696723.1:n.4407A>C
ENST00000696741.1:n.2412A>C
ENST00000696742.1:n.2139A>C
ENST00000696743.1:n.3542A>C
ENST00000696744.1:n.813A>C
ENST00000696767.1:n.1108A>C
ENST00000696768.1:c.*97A>C	ENSP00000512859.1:n.*97A>C
ENST00000696769.1:n.2463A>C
ENST00000696771.1:c.57A>C	ENSP00000512860.1:p.Lys19Asn
ENST00000696772.1:n.2377A>C
ENST00000696773.1:n.2116A>C
ENST00000696774.1:n.5884A>C
ENST00000696776.1:c.867A>C	ENSP00000512861.1:p.Lys289Asn
ENST00000696777.1:n.2182A>C
ENST00000696778.1:n.1210A>C
ENST00000696779.1:c.381A>C	ENSP00000512862.1:p.Lys127Asn
ENST00000696780.1:c.804A>C	ENSP00000512863.1:p.Lys268Asn
ENST00000696781.1:c.519A>C	ENSP00000512864.1:p.Lys173Asn
ENST00000696782.1:c.*176A>C	ENSP00000512865.1:n.*176A>C
ENST00000696783.1:n.2642A>C
ENST00000696992.1:n.1891A>C
ENST00000696995.1:n.4303A>C
ENST00000696996.1:n.2216A>C
ENST00000696997.1:c.*404A>C	ENSP00000513028.1:n.*404A>C
ENST00000696998.1:n.2028A>C
ENST00000696999.1:c.57A>C	ENSP00000513029.1:p.Lys19Asn
ENST00000697035.1:c.*107A>C	ENSP00000513059.1:n.*107A>C
ENST00000697036.1:c.*190A>C	ENSP00000513060.1:n.*190A>C
ENST00000697037.1:n.809A>C
ENST00000697093.1:n.3010A>C
ENST00000697094.1:n.3357A>C
ENST00000697095.1:c.*1975A>C	ENSP00000513104.1:n.*1975A>C
ENST00000697096.1:n.1907A>C
ENST00000697097.1:c.57A>C	ENSP00000513105.1:p.Lys19Asn
ENST00000562983.2:n.960A>C
ENST00000690268.1:c.855A>C	ENSP00000509810.1:p.Lys285Asn
ENST00000355740.7:c.*100A>C	ENSP00000347979.3:n.*100A>C
ENST00000612663.5:c.*176A>C	ENSP00000477997.3:n.*176A>C
ENST00000640140.1:n.946A>C
ENST00000640250.1:n.273A>C
ENST00000640681.1:n.895A>C
ENST00000652046.1:c.774A>C MANE Select	ENSP00000498466.1:p.Lys258Asn
ENST00000352159.8:c.*91A>C	ENSP00000345601.4:n.*91A>C
ENST00000355279.2:c.749A>C	ENSP00000347426.2:n.749A>C
ENST00000355740.6:c.774A>C	ENSP00000347979.2:p.Lys258Asn
ENST00000357339.6:c.711A>C	ENSP00000349896.2:p.Lys237Asn
ENST00000479522.5:c.*203A>C	ENSP00000424113.1:n.*203A>C
ENST00000484444.5:c.*215A>C	ENSP00000420975.1:n.*215A>C
ENST00000488877.5:c.*215A>C	ENSP00000425159.1:n.*215A>C
ENST00000492756.5:c.602A>C	ENSP00000422453.1:n.602A>C
ENST00000494410.5:c.*132A>C	ENSP00000423755.1:n.*132A>C
ENST00000494799.5:n.681A>C
ENST00000612663.4:c.*121A>C	ENSP00000477997.2:n.*121A>C
NM_000043.4:c.774A>C , LRG_134t1:c.774A>C	NP_000034.1:p.Lys258Asn
NM_152871.2:c.711A>C	NP_690610.1:p.Lys237Asn
NM_152872.2:c.*86A>C	NP_690611.1:n.*86A>C
NR_028033.2:n.948A>C
NR_028034.2:n.810A>C
NR_028035.2:n.873A>C
NR_028036.2:n.1011A>C
XM_006717819.2:c.855A>C	XP_006717882.1:p.Lys285Asn
XM_011539764.1:c.936A>C	XP_011538066.1:p.Lys312Asn
XM_011539765.1:c.873A>C	XP_011538067.1:p.Lys291Asn
XM_011539766.1:c.855A>C	XP_011538068.1:p.Lys285Asn
XM_011539767.1:c.819A>C	XP_011538069.1:p.Lys273Asn
XR_945732.1:n.842A>C
XR_945733.1:n.779A>C
NM_000043.5:c.774A>C	NP_000034.1:p.Lys258Asn
NM_001320619.1:c.*97A>C	NP_001307548.1:n.*97A>C
NM_152871.3:c.711A>C	NP_690610.1:p.Lys237Asn
NM_152872.3:c.*86A>C	NP_690611.1:n.*86A>C
NR_028033.3:n.920A>C
NR_028034.3:n.782A>C
NR_028035.3:n.845A>C
NR_028036.3:n.983A>C
NR_135313.1:n.900A>C
NR_135314.1:n.1083A>C
NR_135315.1:n.836A>C
XM_006717819.3:c.855A>C	XP_006717882.1:p.Lys285Asn
XM_011539764.2:c.936A>C	XP_011538066.1:p.Lys312Asn
XM_011539765.2:c.873A>C	XP_011538067.1:p.Lys291Asn
XM_011539766.2:c.855A>C	XP_011538068.1:p.Lys285Asn
XM_011539767.3:c.819A>C	XP_011538069.1:p.Lys273Asn
XR_945732.3:n.842A>C
XR_945733.2:n.779A>C
NM_000043.6:c.774A>C MANE Select	NP_000034.1:p.Lys258Asn
NM_001320619.2:c.*97A>C	NP_001307548.1:n.*97A>C
NM_152871.4:c.711A>C	NP_690610.1:p.Lys237Asn
NM_152872.4:c.*86A>C	NP_690611.1:n.*86A>C
NR_028033.4:n.681A>C
NR_028034.4:n.543A>C
NR_028035.4:n.606A>C
NR_028036.4:n.744A>C
NR_135313.2:n.661A>C
NR_135314.2:n.940A>C
NR_135315.2:n.693A>C