Canonical Allele Identifier: CA377509728

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773956G>A (hg19) ; chr10:g.89014199G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014199G>A , CM000672.2:g.89014199G>A	GRCh38
NC_000010.10:g.90773956G>A , CM000672.1:g.90773956G>A	GRCh37
NC_000010.9:g.90763936G>A	NCBI36
NG_009089.2:g.28669G>A , LRG_134:g.28669G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1066G>A
ENST00000355740.8:c.*80G>A	ENSP00000347979.3:n.*80G>A
ENST00000357339.7:c.694G>A	ENSP00000349896.2:p.Gly232Ser
ENST00000371857.8:n.2302G>A
ENST00000460510.6:c.40G>A	ENSP00000512812.1:p.Gly14Ser
ENST00000466081.6:n.2406G>A
ENST00000477270.6:c.802G>A	ENSP00000512813.1:p.Gly268Ser
ENST00000479522.6:c.*186G>A	ENSP00000424113.1:n.*186G>A
ENST00000484444.6:c.*198G>A	ENSP00000420975.1:n.*198G>A
ENST00000488877.6:c.648G>A	ENSP00000425159.1:n.648G>A
ENST00000492756.7:c.*186G>A	ENSP00000422453.1:n.*186G>A
ENST00000494799.6:c.40G>A	ENSP00000512834.1:p.Gly14Ser
ENST00000562983.3:c.40G>A	ENSP00000512845.1:p.Gly14Ser
ENST00000612663.6:c.*159G>A	ENSP00000477997.3:n.*159G>A
ENST00000640140.2:n.902G>A
ENST00000640250.2:n.256G>A
ENST00000640681.2:n.861G>A
ENST00000696723.1:n.4390G>A
ENST00000696741.1:n.2395G>A
ENST00000696742.1:n.2122G>A
ENST00000696743.1:n.3525G>A
ENST00000696744.1:n.796G>A
ENST00000696767.1:n.1091G>A
ENST00000696768.1:c.*80G>A	ENSP00000512859.1:n.*80G>A
ENST00000696769.1:n.2446G>A
ENST00000696771.1:c.40G>A	ENSP00000512860.1:p.Gly14Ser
ENST00000696772.1:n.2360G>A
ENST00000696773.1:n.2099G>A
ENST00000696774.1:n.5867G>A
ENST00000696776.1:c.850G>A	ENSP00000512861.1:p.Gly284Ser
ENST00000696777.1:n.2165G>A
ENST00000696778.1:n.1193G>A
ENST00000696779.1:c.364G>A	ENSP00000512862.1:p.Gly122Ser
ENST00000696780.1:c.787G>A	ENSP00000512863.1:p.Gly263Ser
ENST00000696781.1:c.502G>A	ENSP00000512864.1:p.Gly168Ser
ENST00000696782.1:c.*159G>A	ENSP00000512865.1:n.*159G>A
ENST00000696783.1:n.2625G>A
ENST00000696992.1:n.1874G>A
ENST00000696995.1:n.4286G>A
ENST00000696996.1:n.2199G>A
ENST00000696997.1:c.*387G>A	ENSP00000513028.1:n.*387G>A
ENST00000696998.1:n.2011G>A
ENST00000696999.1:c.40G>A	ENSP00000513029.1:p.Gly14Ser
ENST00000697035.1:c.*90G>A	ENSP00000513059.1:n.*90G>A
ENST00000697036.1:c.*173G>A	ENSP00000513060.1:n.*173G>A
ENST00000697037.1:n.792G>A
ENST00000697093.1:n.2993G>A
ENST00000697094.1:n.3340G>A
ENST00000697095.1:c.*1958G>A	ENSP00000513104.1:n.*1958G>A
ENST00000697096.1:n.1890G>A
ENST00000697097.1:c.40G>A	ENSP00000513105.1:p.Gly14Ser
ENST00000562983.2:n.943G>A
ENST00000690268.1:c.838G>A	ENSP00000509810.1:p.Gly280Ser
ENST00000355740.7:c.*83G>A	ENSP00000347979.3:n.*83G>A
ENST00000612663.5:c.*159G>A	ENSP00000477997.3:n.*159G>A
ENST00000640140.1:n.929G>A
ENST00000640250.1:n.256G>A
ENST00000640681.1:n.878G>A
ENST00000652046.1:c.757G>A MANE Select	ENSP00000498466.1:p.Gly253Ser
ENST00000352159.8:c.*74G>A	ENSP00000345601.4:n.*74G>A
ENST00000355279.2:c.732G>A	ENSP00000347426.2:n.732G>A
ENST00000355740.6:c.757G>A	ENSP00000347979.2:p.Gly253Ser
ENST00000357339.6:c.694G>A	ENSP00000349896.2:p.Gly232Ser
ENST00000479522.5:c.*186G>A	ENSP00000424113.1:n.*186G>A
ENST00000484444.5:c.*198G>A	ENSP00000420975.1:n.*198G>A
ENST00000488877.5:c.*198G>A	ENSP00000425159.1:n.*198G>A
ENST00000492756.5:c.585G>A	ENSP00000422453.1:n.585G>A
ENST00000494410.5:c.*115G>A	ENSP00000423755.1:n.*115G>A
ENST00000494799.5:n.664G>A
ENST00000612663.4:c.*104G>A	ENSP00000477997.2:n.*104G>A
ENST00000615406.4:c.755G>A	ENSP00000484575.1:p.Trp252Ter
NM_000043.4:c.757G>A , LRG_134t1:c.757G>A	NP_000034.1:p.Gly253Ser
NM_152871.2:c.694G>A	NP_690610.1:p.Gly232Ser
NM_152872.2:c.*69G>A	NP_690611.1:n.*69G>A
NR_028033.2:n.931G>A
NR_028034.2:n.793G>A
NR_028035.2:n.856G>A
NR_028036.2:n.994G>A
XM_006717819.2:c.838G>A	XP_006717882.1:p.Gly280Ser
XM_011539764.1:c.919G>A	XP_011538066.1:p.Gly307Ser
XM_011539765.1:c.856G>A	XP_011538067.1:p.Gly286Ser
XM_011539766.1:c.838G>A	XP_011538068.1:p.Gly280Ser
XM_011539767.1:c.802G>A	XP_011538069.1:p.Gly268Ser
XR_945732.1:n.825G>A
XR_945733.1:n.762G>A
NM_000043.5:c.757G>A	NP_000034.1:p.Gly253Ser
NM_001320619.1:c.*80G>A	NP_001307548.1:n.*80G>A
NM_152871.3:c.694G>A	NP_690610.1:p.Gly232Ser
NM_152872.3:c.*69G>A	NP_690611.1:n.*69G>A
NR_028033.3:n.903G>A
NR_028034.3:n.765G>A
NR_028035.3:n.828G>A
NR_028036.3:n.966G>A
NR_135313.1:n.883G>A
NR_135314.1:n.1066G>A
NR_135315.1:n.819G>A
XM_006717819.3:c.838G>A	XP_006717882.1:p.Gly280Ser
XM_011539764.2:c.919G>A	XP_011538066.1:p.Gly307Ser
XM_011539765.2:c.856G>A	XP_011538067.1:p.Gly286Ser
XM_011539766.2:c.838G>A	XP_011538068.1:p.Gly280Ser
XM_011539767.3:c.802G>A	XP_011538069.1:p.Gly268Ser
XR_945732.3:n.825G>A
XR_945733.2:n.762G>A
NM_000043.6:c.757G>A MANE Select	NP_000034.1:p.Gly253Ser
NM_001320619.2:c.*80G>A	NP_001307548.1:n.*80G>A
NM_152871.4:c.694G>A	NP_690610.1:p.Gly232Ser
NM_152872.4:c.*69G>A	NP_690611.1:n.*69G>A
NR_028033.4:n.664G>A
NR_028034.4:n.526G>A
NR_028035.4:n.589G>A
NR_028036.4:n.727G>A
NR_135313.2:n.644G>A
NR_135314.2:n.923G>A
NR_135315.2:n.676G>A