Canonical Allele Identifier: CA377509920

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774035G>T (hg19) ; chr10:g.89014278G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014278G>T , CM000672.2:g.89014278G>T	GRCh38
NC_000010.10:g.90774035G>T , CM000672.1:g.90774035G>T	GRCh37
NC_000010.9:g.90764015G>T	NCBI36
NG_009089.2:g.28748G>T , LRG_134:g.28748G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1145G>T
ENST00000355740.8:c.*159G>T	ENSP00000347979.3:n.*159G>T
ENST00000357339.7:c.773G>T	ENSP00000349896.2:p.Arg258Leu
ENST00000371857.8:n.2381G>T
ENST00000460510.6:c.119G>T	ENSP00000512812.1:p.Arg40Leu
ENST00000466081.6:n.2485G>T
ENST00000477270.6:c.881G>T	ENSP00000512813.1:p.Arg294Leu
ENST00000479522.6:c.*265G>T	ENSP00000424113.1:n.*265G>T
ENST00000484444.6:c.*277G>T	ENSP00000420975.1:n.*277G>T
ENST00000488877.6:c.727G>T	ENSP00000425159.1:n.727G>T
ENST00000492756.7:c.*265G>T	ENSP00000422453.1:n.*265G>T
ENST00000494799.6:c.119G>T	ENSP00000512834.1:p.Arg40Leu
ENST00000562983.3:c.119G>T	ENSP00000512845.1:p.Arg40Leu
ENST00000612663.6:c.*238G>T	ENSP00000477997.3:n.*238G>T
ENST00000640140.2:n.981G>T
ENST00000640250.2:n.335G>T
ENST00000640681.2:n.940G>T
ENST00000696723.1:n.4469G>T
ENST00000696741.1:n.2474G>T
ENST00000696742.1:n.2201G>T
ENST00000696743.1:n.3604G>T
ENST00000696744.1:n.875G>T
ENST00000696767.1:n.1170G>T
ENST00000696768.1:c.*159G>T	ENSP00000512859.1:n.*159G>T
ENST00000696769.1:n.2525G>T
ENST00000696771.1:c.119G>T	ENSP00000512860.1:p.Arg40Leu
ENST00000696772.1:n.2439G>T
ENST00000696773.1:n.2178G>T
ENST00000696774.1:n.5946G>T
ENST00000696776.1:c.929G>T	ENSP00000512861.1:p.Arg310Leu
ENST00000696777.1:n.2244G>T
ENST00000696778.1:n.1272G>T
ENST00000696779.1:c.443G>T	ENSP00000512862.1:p.Arg148Leu
ENST00000696780.1:c.866G>T	ENSP00000512863.1:p.Arg289Leu
ENST00000696781.1:c.581G>T	ENSP00000512864.1:p.Arg194Leu
ENST00000696782.1:c.*238G>T	ENSP00000512865.1:n.*238G>T
ENST00000696783.1:n.2704G>T
ENST00000696992.1:n.1953G>T
ENST00000696995.1:n.4365G>T
ENST00000696996.1:n.2278G>T
ENST00000696997.1:c.*466G>T	ENSP00000513028.1:n.*466G>T
ENST00000696998.1:n.2090G>T
ENST00000696999.1:c.119G>T	ENSP00000513029.1:p.Arg40Leu
ENST00000697035.1:c.*169G>T	ENSP00000513059.1:n.*169G>T
ENST00000697036.1:c.*252G>T	ENSP00000513060.1:n.*252G>T
ENST00000697037.1:n.871G>T
ENST00000697093.1:n.3072G>T
ENST00000697094.1:n.3419G>T
ENST00000697095.1:c.*2037G>T	ENSP00000513104.1:n.*2037G>T
ENST00000697096.1:n.1969G>T
ENST00000697097.1:c.119G>T	ENSP00000513105.1:p.Arg40Leu
ENST00000562983.2:n.1022G>T
ENST00000690268.1:c.917G>T	ENSP00000509810.1:p.Arg306Leu
ENST00000355740.7:c.*162G>T	ENSP00000347979.3:n.*162G>T
ENST00000612663.5:c.*238G>T	ENSP00000477997.3:n.*238G>T
ENST00000640140.1:n.1008G>T
ENST00000640250.1:n.335G>T
ENST00000640681.1:n.957G>T
ENST00000652046.1:c.836G>T MANE Select	ENSP00000498466.1:p.Arg279Leu
ENST00000352159.8:c.*153G>T	ENSP00000345601.4:n.*153G>T
ENST00000355279.2:c.811G>T	ENSP00000347426.2:n.811G>T
ENST00000355740.6:c.836G>T	ENSP00000347979.2:p.Arg279Leu
ENST00000357339.6:c.773G>T	ENSP00000349896.2:p.Arg258Leu
ENST00000479522.5:c.*265G>T	ENSP00000424113.1:n.*265G>T
ENST00000484444.5:c.*277G>T	ENSP00000420975.1:n.*277G>T
ENST00000488877.5:c.*277G>T	ENSP00000425159.1:n.*277G>T
ENST00000492756.5:c.664G>T	ENSP00000422453.1:n.664G>T
ENST00000494410.5:c.*194G>T	ENSP00000423755.1:n.*194G>T
ENST00000612663.4:c.*183G>T	ENSP00000477997.2:n.*183G>T
NM_000043.4:c.836G>T , LRG_134t1:c.836G>T	NP_000034.1:p.Arg279Leu
NM_152871.2:c.773G>T	NP_690610.1:p.Arg258Leu
NM_152872.2:c.*148G>T	NP_690611.1:n.*148G>T
NR_028033.2:n.1010G>T
NR_028034.2:n.872G>T
NR_028035.2:n.935G>T
NR_028036.2:n.1073G>T
XM_006717819.2:c.917G>T	XP_006717882.1:p.Arg306Leu
XM_011539764.1:c.998G>T	XP_011538066.1:p.Arg333Leu
XM_011539765.1:c.935G>T	XP_011538067.1:p.Arg312Leu
XM_011539766.1:c.917G>T	XP_011538068.1:p.Arg306Leu
XM_011539767.1:c.881G>T	XP_011538069.1:p.Arg294Leu
XR_945732.1:n.904G>T
XR_945733.1:n.841G>T
NM_000043.5:c.836G>T	NP_000034.1:p.Arg279Leu
NM_001320619.1:c.*159G>T	NP_001307548.1:n.*159G>T
NM_152871.3:c.773G>T	NP_690610.1:p.Arg258Leu
NM_152872.3:c.*148G>T	NP_690611.1:n.*148G>T
NR_028033.3:n.982G>T
NR_028034.3:n.844G>T
NR_028035.3:n.907G>T
NR_028036.3:n.1045G>T
NR_135313.1:n.962G>T
NR_135314.1:n.1145G>T
NR_135315.1:n.898G>T
XM_006717819.3:c.917G>T	XP_006717882.1:p.Arg306Leu
XM_011539764.2:c.998G>T	XP_011538066.1:p.Arg333Leu
XM_011539765.2:c.935G>T	XP_011538067.1:p.Arg312Leu
XM_011539766.2:c.917G>T	XP_011538068.1:p.Arg306Leu
XM_011539767.3:c.881G>T	XP_011538069.1:p.Arg294Leu
XR_945732.3:n.904G>T
XR_945733.2:n.841G>T
NM_000043.6:c.836G>T MANE Select	NP_000034.1:p.Arg279Leu
NM_001320619.2:c.*159G>T	NP_001307548.1:n.*159G>T
NM_152871.4:c.773G>T	NP_690610.1:p.Arg258Leu
NM_152872.4:c.*148G>T	NP_690611.1:n.*148G>T
NR_028033.4:n.743G>T
NR_028034.4:n.605G>T
NR_028035.4:n.668G>T
NR_028036.4:n.806G>T
NR_135313.2:n.723G>T
NR_135314.2:n.1002G>T
NR_135315.2:n.755G>T