Canonical Allele Identifier: CA377508576

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90768673G>T (hg19) ; chr10:g.89008916G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89008916G>T , CM000672.2:g.89008916G>T	GRCh38
NC_000010.10:g.90768673G>T , CM000672.1:g.90768673G>T	GRCh37
NC_000010.9:g.90758653G>T	NCBI36
NG_009089.2:g.23386G>T , LRG_134:g.23386G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.671G>T
ENST00000355740.8:c.362G>T	ENSP00000347979.3:p.Arg121Leu
ENST00000357339.7:c.362G>T	ENSP00000349896.2:p.Arg121Leu
ENST00000371857.8:n.572G>T
ENST00000460510.6:c.-356G>T	ENSP00000512812.1:n.-356G>T
ENST00000466081.6:n.503+1079G>T
ENST00000477270.6:c.407G>T	ENSP00000512813.1:p.Arg136Leu
ENST00000479522.6:c.197-1623G>T	ENSP00000424113.1:n.197-1623G>T
ENST00000484444.6:c.197-1623G>T	ENSP00000420975.1:n.197-1623G>T
ENST00000488877.6:c.334+1079G>T	ENSP00000425159.1:n.334+1079G>T
ENST00000492756.7:c.334+1079G>T	ENSP00000422453.1:n.334+1079G>T
ENST00000494799.6:c.-274-1623G>T	ENSP00000512834.1:n.-274-1623G>T
ENST00000562983.3:c.-356G>T	ENSP00000512845.1:n.-356G>T
ENST00000612663.6:c.362G>T	ENSP00000477997.3:p.Arg121Leu
ENST00000640140.2:n.507G>T
ENST00000640681.2:n.466G>T
ENST00000696723.1:n.3995G>T
ENST00000696741.1:n.665G>T
ENST00000696742.1:n.544G>T
ENST00000696743.1:n.534G>T
ENST00000696744.1:n.401G>T
ENST00000696767.1:n.544G>T
ENST00000696768.1:c.362G>T	ENSP00000512859.1:p.Arg121Leu
ENST00000696769.1:n.716G>T
ENST00000696770.1:n.1596G>T
ENST00000696771.1:c.-293G>T	ENSP00000512860.1:n.-293G>T
ENST00000696772.1:n.528G>T
ENST00000696773.1:n.521G>T
ENST00000696774.1:n.584G>T
ENST00000696775.1:n.637G>T
ENST00000696776.1:c.455G>T	ENSP00000512861.1:p.Arg152Leu
ENST00000696777.1:n.516+1079G>T
ENST00000696778.1:n.544G>T
ENST00000696779.1:c.197-1623G>T	ENSP00000512862.1:n.197-1623G>T
ENST00000696780.1:c.455G>T	ENSP00000512863.1:p.Arg152Leu
ENST00000696781.1:c.334+1079G>T	ENSP00000512864.1:n.334+1079G>T
ENST00000696782.1:c.362G>T	ENSP00000512865.1:p.Arg121Leu
ENST00000696992.1:n.1479G>T
ENST00000696995.1:n.544G>T
ENST00000696996.1:n.543G>T
ENST00000696997.1:c.362G>T	ENSP00000513028.1:p.Arg121Leu
ENST00000696998.1:n.363-1623G>T
ENST00000696999.1:c.-212+1079G>T	ENSP00000513029.1:n.-212+1079G>T
ENST00000697035.1:c.362G>T	ENSP00000513059.1:p.Arg121Leu
ENST00000697036.1:c.334+1079G>T	ENSP00000513060.1:n.334+1079G>T
ENST00000697037.1:n.397G>T
ENST00000697093.1:n.586G>T
ENST00000697094.1:n.501G>T
ENST00000697095.1:c.*22G>T	ENSP00000513104.1:n.*22G>T
ENST00000697096.1:n.418G>T
ENST00000697097.1:c.-356G>T	ENSP00000513105.1:n.-356G>T
ENST00000562983.2:n.548G>T
ENST00000690268.1:c.443G>T	ENSP00000509810.1:p.Arg148Leu
ENST00000355740.7:c.362G>T	ENSP00000347979.3:p.Arg121Leu
ENST00000612663.5:c.362G>T	ENSP00000477997.3:p.Arg121Leu
ENST00000640140.1:n.534G>T
ENST00000640681.1:n.483G>T
ENST00000652046.1:c.362G>T MANE Select	ENSP00000498466.1:p.Arg121Leu
ENST00000313771.9:n.671G>T
ENST00000352159.8:c.362G>T	ENSP00000345601.4:p.Arg121Leu
ENST00000355279.2:c.362G>T	ENSP00000347426.2:p.Arg121Leu
ENST00000355740.6:c.362G>T	ENSP00000347979.2:p.Arg121Leu
ENST00000357339.6:c.362G>T	ENSP00000349896.2:p.Arg121Leu
ENST00000371857.7:n.528G>T
ENST00000460510.5:n.729G>T
ENST00000466081.5:n.503+1079G>T
ENST00000477270.5:n.525G>T
ENST00000479522.5:c.197-1623G>T	ENSP00000424113.1:n.197-1623G>T
ENST00000484444.5:c.197-1623G>T	ENSP00000420975.1:n.197-1623G>T
ENST00000487314.1:n.511G>T
ENST00000488877.5:c.334+1079G>T	ENSP00000425159.1:n.334+1079G>T
ENST00000492756.5:c.334+1079G>T	ENSP00000422453.1:n.334+1079G>T
ENST00000494410.5:c.334+1079G>T	ENSP00000423755.1:n.334+1079G>T
ENST00000494799.5:n.351-1623G>T
ENST00000612663.4:c.362G>T	ENSP00000477997.2:p.Arg121Leu
ENST00000615406.4:c.362G>T	ENSP00000484575.1:p.Arg121Leu
ENST00000626542.2:c.362G>T	ENSP00000485876.1:p.Arg121Leu
NM_000043.4:c.362G>T , LRG_134t1:c.362G>T	NP_000034.1:p.Arg121Leu
NM_152871.2:c.362G>T	NP_690610.1:p.Arg121Leu
NM_152872.2:c.362G>T	NP_690611.1:p.Arg121Leu
NR_028033.2:n.680+1079G>T
NR_028034.2:n.543-1623G>T
NR_028035.2:n.543-1623G>T
NR_028036.2:n.680+1079G>T
XM_006717819.2:c.443G>T	XP_006717882.1:p.Arg148Leu
XM_011539764.1:c.524G>T	XP_011538066.1:p.Arg175Leu
XM_011539765.1:c.524G>T	XP_011538067.1:p.Arg175Leu
XM_011539766.1:c.443G>T	XP_011538068.1:p.Arg148Leu
XM_011539767.1:c.407G>T	XP_011538069.1:p.Arg136Leu
XR_945732.1:n.511+1079G>T
XR_945733.1:n.511+1079G>T
NM_000043.5:c.362G>T	NP_000034.1:p.Arg121Leu
NM_001320619.1:c.362G>T	NP_001307548.1:p.Arg121Leu
NM_152871.3:c.362G>T	NP_690610.1:p.Arg121Leu
NM_152872.3:c.362G>T	NP_690611.1:p.Arg121Leu
NR_028033.3:n.652+1079G>T
NR_028034.3:n.515-1623G>T
NR_028035.3:n.515-1623G>T
NR_028036.3:n.652+1079G>T
NR_135313.1:n.652+1079G>T
NR_135314.1:n.671G>T
NR_135315.1:n.506-1623G>T
XM_006717819.3:c.443G>T	XP_006717882.1:p.Arg148Leu
XM_011539764.2:c.524G>T	XP_011538066.1:p.Arg175Leu
XM_011539765.2:c.524G>T	XP_011538067.1:p.Arg175Leu
XM_011539766.2:c.443G>T	XP_011538068.1:p.Arg148Leu
XM_011539767.3:c.407G>T	XP_011538069.1:p.Arg136Leu
XR_945732.3:n.511+1079G>T
XR_945733.2:n.511+1079G>T
NM_000043.6:c.362G>T MANE Select	NP_000034.1:p.Arg121Leu
NM_001320619.2:c.362G>T	NP_001307548.1:p.Arg121Leu
NM_152871.4:c.362G>T	NP_690610.1:p.Arg121Leu
NM_152872.4:c.362G>T	NP_690611.1:p.Arg121Leu
NR_028033.4:n.413+1079G>T
NR_028034.4:n.276-1623G>T
NR_028035.4:n.276-1623G>T
NR_028036.4:n.413+1079G>T
NR_135313.2:n.413+1079G>T
NR_135314.2:n.528G>T
NR_135315.2:n.363-1623G>T