Canonical Allele Identifier: CA377509883

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774018G>C (hg19) ; chr10:g.89014261G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014261G>C , CM000672.2:g.89014261G>C	GRCh38
NC_000010.10:g.90774018G>C , CM000672.1:g.90774018G>C	GRCh37
NC_000010.9:g.90763998G>C	NCBI36
NG_009089.2:g.28731G>C , LRG_134:g.28731G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.1128G>C
ENST00000355740.8:c.*142G>C	ENSP00000347979.3:n.*142G>C
ENST00000357339.7:c.756G>C	ENSP00000349896.2:p.Gln252His
ENST00000371857.8:n.2364G>C
ENST00000460510.6:c.102G>C	ENSP00000512812.1:p.Gln34His
ENST00000466081.6:n.2468G>C
ENST00000477270.6:c.864G>C	ENSP00000512813.1:p.Gln288His
ENST00000479522.6:c.*248G>C	ENSP00000424113.1:n.*248G>C
ENST00000484444.6:c.*260G>C	ENSP00000420975.1:n.*260G>C
ENST00000488877.6:c.710G>C	ENSP00000425159.1:n.710G>C
ENST00000492756.7:c.*248G>C	ENSP00000422453.1:n.*248G>C
ENST00000494799.6:c.102G>C	ENSP00000512834.1:p.Gln34His
ENST00000562983.3:c.102G>C	ENSP00000512845.1:p.Gln34His
ENST00000612663.6:c.*221G>C	ENSP00000477997.3:n.*221G>C
ENST00000640140.2:n.964G>C
ENST00000640250.2:n.318G>C
ENST00000640681.2:n.923G>C
ENST00000696723.1:n.4452G>C
ENST00000696741.1:n.2457G>C
ENST00000696742.1:n.2184G>C
ENST00000696743.1:n.3587G>C
ENST00000696744.1:n.858G>C
ENST00000696767.1:n.1153G>C
ENST00000696768.1:c.*142G>C	ENSP00000512859.1:n.*142G>C
ENST00000696769.1:n.2508G>C
ENST00000696771.1:c.102G>C	ENSP00000512860.1:p.Gln34His
ENST00000696772.1:n.2422G>C
ENST00000696773.1:n.2161G>C
ENST00000696774.1:n.5929G>C
ENST00000696776.1:c.912G>C	ENSP00000512861.1:p.Gln304His
ENST00000696777.1:n.2227G>C
ENST00000696778.1:n.1255G>C
ENST00000696779.1:c.426G>C	ENSP00000512862.1:p.Gln142His
ENST00000696780.1:c.849G>C	ENSP00000512863.1:p.Gln283His
ENST00000696781.1:c.564G>C	ENSP00000512864.1:p.Gln188His
ENST00000696782.1:c.*221G>C	ENSP00000512865.1:n.*221G>C
ENST00000696783.1:n.2687G>C
ENST00000696992.1:n.1936G>C
ENST00000696995.1:n.4348G>C
ENST00000696996.1:n.2261G>C
ENST00000696997.1:c.*449G>C	ENSP00000513028.1:n.*449G>C
ENST00000696998.1:n.2073G>C
ENST00000696999.1:c.102G>C	ENSP00000513029.1:p.Gln34His
ENST00000697035.1:c.*152G>C	ENSP00000513059.1:n.*152G>C
ENST00000697036.1:c.*235G>C	ENSP00000513060.1:n.*235G>C
ENST00000697037.1:n.854G>C
ENST00000697093.1:n.3055G>C
ENST00000697094.1:n.3402G>C
ENST00000697095.1:c.*2020G>C	ENSP00000513104.1:n.*2020G>C
ENST00000697096.1:n.1952G>C
ENST00000697097.1:c.102G>C	ENSP00000513105.1:p.Gln34His
ENST00000562983.2:n.1005G>C
ENST00000690268.1:c.900G>C	ENSP00000509810.1:p.Gln300His
ENST00000355740.7:c.*145G>C	ENSP00000347979.3:n.*145G>C
ENST00000612663.5:c.*221G>C	ENSP00000477997.3:n.*221G>C
ENST00000640140.1:n.991G>C
ENST00000640250.1:n.318G>C
ENST00000640681.1:n.940G>C
ENST00000652046.1:c.819G>C MANE Select	ENSP00000498466.1:p.Gln273His
ENST00000352159.8:c.*136G>C	ENSP00000345601.4:n.*136G>C
ENST00000355279.2:c.794G>C	ENSP00000347426.2:n.794G>C
ENST00000355740.6:c.819G>C	ENSP00000347979.2:p.Gln273His
ENST00000357339.6:c.756G>C	ENSP00000349896.2:p.Gln252His
ENST00000479522.5:c.*248G>C	ENSP00000424113.1:n.*248G>C
ENST00000484444.5:c.*260G>C	ENSP00000420975.1:n.*260G>C
ENST00000488877.5:c.*260G>C	ENSP00000425159.1:n.*260G>C
ENST00000492756.5:c.647G>C	ENSP00000422453.1:n.647G>C
ENST00000494410.5:c.*177G>C	ENSP00000423755.1:n.*177G>C
ENST00000612663.4:c.*166G>C	ENSP00000477997.2:n.*166G>C
NM_000043.4:c.819G>C , LRG_134t1:c.819G>C	NP_000034.1:p.Gln273His
NM_152871.2:c.756G>C	NP_690610.1:p.Gln252His
NM_152872.2:c.*131G>C	NP_690611.1:n.*131G>C
NR_028033.2:n.993G>C
NR_028034.2:n.855G>C
NR_028035.2:n.918G>C
NR_028036.2:n.1056G>C
XM_006717819.2:c.900G>C	XP_006717882.1:p.Gln300His
XM_011539764.1:c.981G>C	XP_011538066.1:p.Gln327His
XM_011539765.1:c.918G>C	XP_011538067.1:p.Gln306His
XM_011539766.1:c.900G>C	XP_011538068.1:p.Gln300His
XM_011539767.1:c.864G>C	XP_011538069.1:p.Gln288His
XR_945732.1:n.887G>C
XR_945733.1:n.824G>C
NM_000043.5:c.819G>C	NP_000034.1:p.Gln273His
NM_001320619.1:c.*142G>C	NP_001307548.1:n.*142G>C
NM_152871.3:c.756G>C	NP_690610.1:p.Gln252His
NM_152872.3:c.*131G>C	NP_690611.1:n.*131G>C
NR_028033.3:n.965G>C
NR_028034.3:n.827G>C
NR_028035.3:n.890G>C
NR_028036.3:n.1028G>C
NR_135313.1:n.945G>C
NR_135314.1:n.1128G>C
NR_135315.1:n.881G>C
XM_006717819.3:c.900G>C	XP_006717882.1:p.Gln300His
XM_011539764.2:c.981G>C	XP_011538066.1:p.Gln327His
XM_011539765.2:c.918G>C	XP_011538067.1:p.Gln306His
XM_011539766.2:c.900G>C	XP_011538068.1:p.Gln300His
XM_011539767.3:c.864G>C	XP_011538069.1:p.Gln288His
XR_945732.3:n.887G>C
XR_945733.2:n.824G>C
NM_000043.6:c.819G>C MANE Select	NP_000034.1:p.Gln273His
NM_001320619.2:c.*142G>C	NP_001307548.1:n.*142G>C
NM_152871.4:c.756G>C	NP_690610.1:p.Gln252His
NM_152872.4:c.*131G>C	NP_690611.1:n.*131G>C
NR_028033.4:n.726G>C
NR_028034.4:n.588G>C
NR_028035.4:n.651G>C
NR_028036.4:n.789G>C
NR_135313.2:n.706G>C
NR_135314.2:n.985G>C
NR_135315.2:n.738G>C