Canonical Allele Identifier: CA377509713

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773950A>C (hg19) ; chr10:g.89014193A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014193A>C , CM000672.2:g.89014193A>C	GRCh38
NC_000010.10:g.90773950A>C , CM000672.1:g.90773950A>C	GRCh37
NC_000010.9:g.90763930A>C	NCBI36
NG_009089.2:g.28663A>C , LRG_134:g.28663A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1060A>C
ENST00000355740.8:c.*74A>C	ENSP00000347979.3:n.*74A>C
ENST00000357339.7:c.688A>C	ENSP00000349896.2:p.Lys230Gln
ENST00000371857.8:n.2296A>C
ENST00000460510.6:c.34A>C	ENSP00000512812.1:p.Lys12Gln
ENST00000466081.6:n.2400A>C
ENST00000477270.6:c.796A>C	ENSP00000512813.1:p.Lys266Gln
ENST00000479522.6:c.*180A>C	ENSP00000424113.1:n.*180A>C
ENST00000484444.6:c.*192A>C	ENSP00000420975.1:n.*192A>C
ENST00000488877.6:c.642A>C	ENSP00000425159.1:n.642A>C
ENST00000492756.7:c.*180A>C	ENSP00000422453.1:n.*180A>C
ENST00000494799.6:c.34A>C	ENSP00000512834.1:p.Lys12Gln
ENST00000562983.3:c.34A>C	ENSP00000512845.1:p.Lys12Gln
ENST00000612663.6:c.*153A>C	ENSP00000477997.3:n.*153A>C
ENST00000640140.2:n.896A>C
ENST00000640250.2:n.250A>C
ENST00000640681.2:n.855A>C
ENST00000696723.1:n.4384A>C
ENST00000696741.1:n.2389A>C
ENST00000696742.1:n.2116A>C
ENST00000696743.1:n.3519A>C
ENST00000696744.1:n.790A>C
ENST00000696767.1:n.1085A>C
ENST00000696768.1:c.*74A>C	ENSP00000512859.1:n.*74A>C
ENST00000696769.1:n.2440A>C
ENST00000696771.1:c.34A>C	ENSP00000512860.1:p.Lys12Gln
ENST00000696772.1:n.2354A>C
ENST00000696773.1:n.2093A>C
ENST00000696774.1:n.5861A>C
ENST00000696776.1:c.844A>C	ENSP00000512861.1:p.Lys282Gln
ENST00000696777.1:n.2159A>C
ENST00000696778.1:n.1187A>C
ENST00000696779.1:c.358A>C	ENSP00000512862.1:p.Lys120Gln
ENST00000696780.1:c.781A>C	ENSP00000512863.1:p.Lys261Gln
ENST00000696781.1:c.496A>C	ENSP00000512864.1:p.Lys166Gln
ENST00000696782.1:c.*153A>C	ENSP00000512865.1:n.*153A>C
ENST00000696783.1:n.2619A>C
ENST00000696992.1:n.1868A>C
ENST00000696995.1:n.4280A>C
ENST00000696996.1:n.2193A>C
ENST00000696997.1:c.*381A>C	ENSP00000513028.1:n.*381A>C
ENST00000696998.1:n.2005A>C
ENST00000696999.1:c.34A>C	ENSP00000513029.1:p.Lys12Gln
ENST00000697035.1:c.*84A>C	ENSP00000513059.1:n.*84A>C
ENST00000697036.1:c.*167A>C	ENSP00000513060.1:n.*167A>C
ENST00000697037.1:n.786A>C
ENST00000697093.1:n.2987A>C
ENST00000697094.1:n.3334A>C
ENST00000697095.1:c.*1952A>C	ENSP00000513104.1:n.*1952A>C
ENST00000697096.1:n.1884A>C
ENST00000697097.1:c.34A>C	ENSP00000513105.1:p.Lys12Gln
ENST00000562983.2:n.937A>C
ENST00000690268.1:c.832A>C	ENSP00000509810.1:p.Lys278Gln
ENST00000355740.7:c.*77A>C	ENSP00000347979.3:n.*77A>C
ENST00000612663.5:c.*153A>C	ENSP00000477997.3:n.*153A>C
ENST00000640140.1:n.923A>C
ENST00000640250.1:n.250A>C
ENST00000640681.1:n.872A>C
ENST00000652046.1:c.751A>C MANE Select	ENSP00000498466.1:p.Lys251Gln
ENST00000352159.8:c.*68A>C	ENSP00000345601.4:n.*68A>C
ENST00000355279.2:c.726A>C	ENSP00000347426.2:n.726A>C
ENST00000355740.6:c.751A>C	ENSP00000347979.2:p.Lys251Gln
ENST00000357339.6:c.688A>C	ENSP00000349896.2:p.Lys230Gln
ENST00000479522.5:c.*180A>C	ENSP00000424113.1:n.*180A>C
ENST00000484444.5:c.*192A>C	ENSP00000420975.1:n.*192A>C
ENST00000488877.5:c.*192A>C	ENSP00000425159.1:n.*192A>C
ENST00000492756.5:c.579A>C	ENSP00000422453.1:n.579A>C
ENST00000494410.5:c.*109A>C	ENSP00000423755.1:n.*109A>C
ENST00000494799.5:n.658A>C
ENST00000612663.4:c.*98A>C	ENSP00000477997.2:n.*98A>C
ENST00000615406.4:c.751-2A>C	ENSP00000484575.1:n.751-2A>C
NM_000043.4:c.751A>C , LRG_134t1:c.751A>C	NP_000034.1:p.Lys251Gln
NM_152871.2:c.688A>C	NP_690610.1:p.Lys230Gln
NM_152872.2:c.*63A>C	NP_690611.1:n.*63A>C
NR_028033.2:n.925A>C
NR_028034.2:n.787A>C
NR_028035.2:n.850A>C
NR_028036.2:n.988A>C
XM_006717819.2:c.832A>C	XP_006717882.1:p.Lys278Gln
XM_011539764.1:c.913A>C	XP_011538066.1:p.Lys305Gln
XM_011539765.1:c.850A>C	XP_011538067.1:p.Lys284Gln
XM_011539766.1:c.832A>C	XP_011538068.1:p.Lys278Gln
XM_011539767.1:c.796A>C	XP_011538069.1:p.Lys266Gln
XR_945732.1:n.819A>C
XR_945733.1:n.756A>C
NM_000043.5:c.751A>C	NP_000034.1:p.Lys251Gln
NM_001320619.1:c.*74A>C	NP_001307548.1:n.*74A>C
NM_152871.3:c.688A>C	NP_690610.1:p.Lys230Gln
NM_152872.3:c.*63A>C	NP_690611.1:n.*63A>C
NR_028033.3:n.897A>C
NR_028034.3:n.759A>C
NR_028035.3:n.822A>C
NR_028036.3:n.960A>C
NR_135313.1:n.877A>C
NR_135314.1:n.1060A>C
NR_135315.1:n.813A>C
XM_006717819.3:c.832A>C	XP_006717882.1:p.Lys278Gln
XM_011539764.2:c.913A>C	XP_011538066.1:p.Lys305Gln
XM_011539765.2:c.850A>C	XP_011538067.1:p.Lys284Gln
XM_011539766.2:c.832A>C	XP_011538068.1:p.Lys278Gln
XM_011539767.3:c.796A>C	XP_011538069.1:p.Lys266Gln
XR_945732.3:n.819A>C
XR_945733.2:n.756A>C
NM_000043.6:c.751A>C MANE Select	NP_000034.1:p.Lys251Gln
NM_001320619.2:c.*74A>C	NP_001307548.1:n.*74A>C
NM_152871.4:c.688A>C	NP_690610.1:p.Lys230Gln
NM_152872.4:c.*63A>C	NP_690611.1:n.*63A>C
NR_028033.4:n.658A>C
NR_028034.4:n.520A>C
NR_028035.4:n.583A>C
NR_028036.4:n.721A>C
NR_135313.2:n.638A>C
NR_135314.2:n.917A>C
NR_135315.2:n.670A>C