Canonical Allele Identifier: CA377509971

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774056G>C (hg19) ; chr10:g.89014299G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014299G>C , CM000672.2:g.89014299G>C	GRCh38
NC_000010.10:g.90774056G>C , CM000672.1:g.90774056G>C	GRCh37
NC_000010.9:g.90764036G>C	NCBI36
NG_009089.2:g.28769G>C , LRG_134:g.28769G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1166G>C
ENST00000355740.8:c.*180G>C	ENSP00000347979.3:n.*180G>C
ENST00000357339.7:c.794G>C	ENSP00000349896.2:p.Gly265Ala
ENST00000371857.8:n.2402G>C
ENST00000460510.6:c.140G>C	ENSP00000512812.1:p.Gly47Ala
ENST00000466081.6:n.2506G>C
ENST00000477270.6:c.902G>C	ENSP00000512813.1:p.Gly301Ala
ENST00000479522.6:c.*286G>C	ENSP00000424113.1:n.*286G>C
ENST00000484444.6:c.*298G>C	ENSP00000420975.1:n.*298G>C
ENST00000488877.6:c.748G>C	ENSP00000425159.1:n.748G>C
ENST00000492756.7:c.*286G>C	ENSP00000422453.1:n.*286G>C
ENST00000494799.6:c.140G>C	ENSP00000512834.1:p.Gly47Ala
ENST00000562983.3:c.140G>C	ENSP00000512845.1:p.Gly47Ala
ENST00000612663.6:c.*259G>C	ENSP00000477997.3:n.*259G>C
ENST00000640140.2:n.1002G>C
ENST00000640250.2:n.356G>C
ENST00000640681.2:n.961G>C
ENST00000696723.1:n.4490G>C
ENST00000696741.1:n.2495G>C
ENST00000696742.1:n.2222G>C
ENST00000696743.1:n.3625G>C
ENST00000696744.1:n.896G>C
ENST00000696767.1:n.1191G>C
ENST00000696768.1:c.*180G>C	ENSP00000512859.1:n.*180G>C
ENST00000696769.1:n.2546G>C
ENST00000696771.1:c.140G>C	ENSP00000512860.1:p.Gly47Ala
ENST00000696772.1:n.2460G>C
ENST00000696773.1:n.2199G>C
ENST00000696774.1:n.5967G>C
ENST00000696776.1:c.950G>C	ENSP00000512861.1:p.Gly317Ala
ENST00000696777.1:n.2265G>C
ENST00000696778.1:n.1293G>C
ENST00000696779.1:c.464G>C	ENSP00000512862.1:p.Gly155Ala
ENST00000696780.1:c.887G>C	ENSP00000512863.1:p.Gly296Ala
ENST00000696781.1:c.602G>C	ENSP00000512864.1:p.Gly201Ala
ENST00000696782.1:c.*259G>C	ENSP00000512865.1:n.*259G>C
ENST00000696783.1:n.2725G>C
ENST00000696992.1:n.1974G>C
ENST00000696995.1:n.4386G>C
ENST00000696996.1:n.2299G>C
ENST00000696997.1:c.*487G>C	ENSP00000513028.1:n.*487G>C
ENST00000696998.1:n.2111G>C
ENST00000696999.1:c.140G>C	ENSP00000513029.1:p.Gly47Ala
ENST00000697035.1:c.*190G>C	ENSP00000513059.1:n.*190G>C
ENST00000697036.1:c.*273G>C	ENSP00000513060.1:n.*273G>C
ENST00000697037.1:n.892G>C
ENST00000697093.1:n.3093G>C
ENST00000697094.1:n.3440G>C
ENST00000697095.1:c.*2058G>C	ENSP00000513104.1:n.*2058G>C
ENST00000697096.1:n.1990G>C
ENST00000697097.1:c.140G>C	ENSP00000513105.1:p.Gly47Ala
ENST00000562983.2:n.1043G>C
ENST00000690268.1:c.938G>C	ENSP00000509810.1:p.Gly313Ala
ENST00000355740.7:c.*183G>C	ENSP00000347979.3:n.*183G>C
ENST00000612663.5:c.*259G>C	ENSP00000477997.3:n.*259G>C
ENST00000640140.1:n.1029G>C
ENST00000640250.1:n.356G>C
ENST00000640681.1:n.978G>C
ENST00000652046.1:c.857G>C MANE Select	ENSP00000498466.1:p.Gly286Ala
ENST00000352159.8:c.*174G>C	ENSP00000345601.4:n.*174G>C
ENST00000355279.2:c.832G>C	ENSP00000347426.2:n.832G>C
ENST00000355740.6:c.857G>C	ENSP00000347979.2:p.Gly286Ala
ENST00000357339.6:c.794G>C	ENSP00000349896.2:p.Gly265Ala
ENST00000479522.5:c.*286G>C	ENSP00000424113.1:n.*286G>C
ENST00000484444.5:c.*298G>C	ENSP00000420975.1:n.*298G>C
ENST00000488877.5:c.*298G>C	ENSP00000425159.1:n.*298G>C
ENST00000492756.5:c.685G>C	ENSP00000422453.1:n.685G>C
ENST00000494410.5:c.*215G>C	ENSP00000423755.1:n.*215G>C
ENST00000612663.4:c.*204G>C	ENSP00000477997.2:n.*204G>C
NM_000043.4:c.857G>C , LRG_134t1:c.857G>C	NP_000034.1:p.Gly286Ala
NM_152871.2:c.794G>C	NP_690610.1:p.Gly265Ala
NM_152872.2:c.*169G>C	NP_690611.1:n.*169G>C
NR_028033.2:n.1031G>C
NR_028034.2:n.893G>C
NR_028035.2:n.956G>C
NR_028036.2:n.1094G>C
XM_006717819.2:c.938G>C	XP_006717882.1:p.Gly313Ala
XM_011539764.1:c.1019G>C	XP_011538066.1:p.Gly340Ala
XM_011539765.1:c.956G>C	XP_011538067.1:p.Gly319Ala
XM_011539766.1:c.938G>C	XP_011538068.1:p.Gly313Ala
XM_011539767.1:c.902G>C	XP_011538069.1:p.Gly301Ala
XR_945732.1:n.925G>C
XR_945733.1:n.862G>C
NM_000043.5:c.857G>C	NP_000034.1:p.Gly286Ala
NM_001320619.1:c.*180G>C	NP_001307548.1:n.*180G>C
NM_152871.3:c.794G>C	NP_690610.1:p.Gly265Ala
NM_152872.3:c.*169G>C	NP_690611.1:n.*169G>C
NR_028033.3:n.1003G>C
NR_028034.3:n.865G>C
NR_028035.3:n.928G>C
NR_028036.3:n.1066G>C
NR_135313.1:n.983G>C
NR_135314.1:n.1166G>C
NR_135315.1:n.919G>C
XM_006717819.3:c.938G>C	XP_006717882.1:p.Gly313Ala
XM_011539764.2:c.1019G>C	XP_011538066.1:p.Gly340Ala
XM_011539765.2:c.956G>C	XP_011538067.1:p.Gly319Ala
XM_011539766.2:c.938G>C	XP_011538068.1:p.Gly313Ala
XM_011539767.3:c.902G>C	XP_011538069.1:p.Gly301Ala
XR_945732.3:n.925G>C
XR_945733.2:n.862G>C
NM_000043.6:c.857G>C MANE Select	NP_000034.1:p.Gly286Ala
NM_001320619.2:c.*180G>C	NP_001307548.1:n.*180G>C
NM_152871.4:c.794G>C	NP_690610.1:p.Gly265Ala
NM_152872.4:c.*169G>C	NP_690611.1:n.*169G>C
NR_028033.4:n.764G>C
NR_028034.4:n.626G>C
NR_028035.4:n.689G>C
NR_028036.4:n.827G>C
NR_135313.2:n.744G>C
NR_135314.2:n.1023G>C
NR_135315.2:n.776G>C