Canonical Allele Identifier: CA470974945

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773937A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014180A>G , CM000672.2:g.89014180A>G	GRCh38
NC_000010.10:g.90773937A>G , CM000672.1:g.90773937A>G	GRCh37
NC_000010.9:g.90763917A>G	NCBI36
NG_009089.2:g.28650A>G , LRG_134:g.28650A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1047A>G
ENST00000355740.8:c.*61A>G	ENSP00000347979.3:n.*61A>G
ENST00000357339.7:c.675A>G	ENSP00000349896.2:p.Lys225=
ENST00000371857.8:n.2283A>G
ENST00000460510.6:c.21A>G	ENSP00000512812.1:p.Lys7=
ENST00000466081.6:n.2387A>G
ENST00000477270.6:c.783A>G	ENSP00000512813.1:p.Lys261=
ENST00000479522.6:c.*167A>G	ENSP00000424113.1:n.*167A>G
ENST00000484444.6:c.*179A>G	ENSP00000420975.1:n.*179A>G
ENST00000488877.6:c.629A>G	ENSP00000425159.1:n.629A>G
ENST00000492756.7:c.*167A>G	ENSP00000422453.1:n.*167A>G
ENST00000494799.6:c.21A>G	ENSP00000512834.1:p.Lys7=
ENST00000562983.3:c.21A>G	ENSP00000512845.1:p.Lys7=
ENST00000612663.6:c.*140A>G	ENSP00000477997.3:n.*140A>G
ENST00000640140.2:n.883A>G
ENST00000640250.2:n.237A>G
ENST00000640681.2:n.842A>G
ENST00000696723.1:n.4371A>G
ENST00000696741.1:n.2376A>G
ENST00000696742.1:n.2103A>G
ENST00000696743.1:n.3506A>G
ENST00000696744.1:n.777A>G
ENST00000696767.1:n.1072A>G
ENST00000696768.1:c.*61A>G	ENSP00000512859.1:n.*61A>G
ENST00000696769.1:n.2427A>G
ENST00000696771.1:c.21A>G	ENSP00000512860.1:p.Lys7=
ENST00000696772.1:n.2341A>G
ENST00000696773.1:n.2080A>G
ENST00000696774.1:n.5848A>G
ENST00000696776.1:c.831A>G	ENSP00000512861.1:p.Lys277=
ENST00000696777.1:n.2146A>G
ENST00000696778.1:n.1174A>G
ENST00000696779.1:c.345A>G	ENSP00000512862.1:p.Lys115=
ENST00000696780.1:c.768A>G	ENSP00000512863.1:p.Lys256=
ENST00000696781.1:c.483A>G	ENSP00000512864.1:p.Lys161=
ENST00000696782.1:c.*140A>G	ENSP00000512865.1:n.*140A>G
ENST00000696783.1:n.2606A>G
ENST00000696992.1:n.1855A>G
ENST00000696995.1:n.4267A>G
ENST00000696996.1:n.2180A>G
ENST00000696997.1:c.*368A>G	ENSP00000513028.1:n.*368A>G
ENST00000696998.1:n.1992A>G
ENST00000696999.1:c.21A>G	ENSP00000513029.1:p.Lys7=
ENST00000697035.1:c.*71A>G	ENSP00000513059.1:n.*71A>G
ENST00000697036.1:c.*154A>G	ENSP00000513060.1:n.*154A>G
ENST00000697037.1:n.773A>G
ENST00000697093.1:n.2974A>G
ENST00000697094.1:n.3321A>G
ENST00000697095.1:c.*1939A>G	ENSP00000513104.1:n.*1939A>G
ENST00000697096.1:n.1871A>G
ENST00000697097.1:c.21A>G	ENSP00000513105.1:p.Lys7=
ENST00000562983.2:n.924A>G
ENST00000690268.1:c.819A>G	ENSP00000509810.1:p.Lys273=
ENST00000355740.7:c.*64A>G	ENSP00000347979.3:n.*64A>G
ENST00000612663.5:c.*140A>G	ENSP00000477997.3:n.*140A>G
ENST00000640140.1:n.910A>G
ENST00000640250.1:n.237A>G
ENST00000640681.1:n.859A>G
ENST00000652046.1:c.738A>G MANE Select	ENSP00000498466.1:p.Lys246=
ENST00000352159.8:c.*55A>G	ENSP00000345601.4:n.*55A>G
ENST00000355279.2:c.713A>G	ENSP00000347426.2:n.713A>G
ENST00000355740.6:c.738A>G	ENSP00000347979.2:p.Lys246=
ENST00000357339.6:c.675A>G	ENSP00000349896.2:p.Lys225=
ENST00000479522.5:c.*167A>G	ENSP00000424113.1:n.*167A>G
ENST00000484444.5:c.*179A>G	ENSP00000420975.1:n.*179A>G
ENST00000488877.5:c.*179A>G	ENSP00000425159.1:n.*179A>G
ENST00000492756.5:c.566A>G	ENSP00000422453.1:n.566A>G
ENST00000494410.5:c.*96A>G	ENSP00000423755.1:n.*96A>G
ENST00000494799.5:n.645A>G
ENST00000612663.4:c.*85A>G	ENSP00000477997.2:n.*85A>G
ENST00000615406.4:c.738A>G	ENSP00000484575.1:p.Lys246=
NM_000043.4:c.738A>G , LRG_134t1:c.738A>G	NP_000034.1:p.Lys246=
NM_152871.2:c.675A>G	NP_690610.1:p.Lys225=
NM_152872.2:c.*50A>G	NP_690611.1:n.*50A>G
NR_028033.2:n.912A>G
NR_028034.2:n.774A>G
NR_028035.2:n.837A>G
NR_028036.2:n.975A>G
XM_006717819.2:c.819A>G	XP_006717882.1:p.Lys273=
XM_011539764.1:c.900A>G	XP_011538066.1:p.Lys300=
XM_011539765.1:c.837A>G	XP_011538067.1:p.Lys279=
XM_011539766.1:c.819A>G	XP_011538068.1:p.Lys273=
XM_011539767.1:c.783A>G	XP_011538069.1:p.Lys261=
XR_945732.1:n.806A>G
XR_945733.1:n.743A>G
NM_000043.5:c.738A>G	NP_000034.1:p.Lys246=
NM_001320619.1:c.*61A>G	NP_001307548.1:n.*61A>G
NM_152871.3:c.675A>G	NP_690610.1:p.Lys225=
NM_152872.3:c.*50A>G	NP_690611.1:n.*50A>G
NR_028033.3:n.884A>G
NR_028034.3:n.746A>G
NR_028035.3:n.809A>G
NR_028036.3:n.947A>G
NR_135313.1:n.864A>G
NR_135314.1:n.1047A>G
NR_135315.1:n.800A>G
XM_006717819.3:c.819A>G	XP_006717882.1:p.Lys273=
XM_011539764.2:c.900A>G	XP_011538066.1:p.Lys300=
XM_011539765.2:c.837A>G	XP_011538067.1:p.Lys279=
XM_011539766.2:c.819A>G	XP_011538068.1:p.Lys273=
XM_011539767.3:c.783A>G	XP_011538069.1:p.Lys261=
XR_945732.3:n.806A>G
XR_945733.2:n.743A>G
NM_000043.6:c.738A>G MANE Select	NP_000034.1:p.Lys246=
NM_001320619.2:c.*61A>G	NP_001307548.1:n.*61A>G
NM_152871.4:c.675A>G	NP_690610.1:p.Lys225=
NM_152872.4:c.*50A>G	NP_690611.1:n.*50A>G
NR_028033.4:n.645A>G
NR_028034.4:n.507A>G
NR_028035.4:n.570A>G
NR_028036.4:n.708A>G
NR_135313.2:n.625A>G
NR_135314.2:n.904A>G
NR_135315.2:n.657A>G