Canonical Allele Identifier: CA377509838

Gene: FAS

Linked Data

• gnomAD v4: 10-89014241-G-A
• MyVariant Identifiers: chr10:g.90773998G>A (hg19) ; chr10:g.89014241G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014241G>A , CM000672.2:g.89014241G>A	GRCh38
NC_000010.10:g.90773998G>A , CM000672.1:g.90773998G>A	GRCh37
NC_000010.9:g.90763978G>A	NCBI36
NG_009089.2:g.28711G>A , LRG_134:g.28711G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1108G>A
ENST00000355740.8:c.*122G>A	ENSP00000347979.3:n.*122G>A
ENST00000357339.7:c.736G>A	ENSP00000349896.2:p.Val246Ile
ENST00000371857.8:n.2344G>A
ENST00000460510.6:c.82G>A	ENSP00000512812.1:p.Val28Ile
ENST00000466081.6:n.2448G>A
ENST00000477270.6:c.844G>A	ENSP00000512813.1:p.Val282Ile
ENST00000479522.6:c.*228G>A	ENSP00000424113.1:n.*228G>A
ENST00000484444.6:c.*240G>A	ENSP00000420975.1:n.*240G>A
ENST00000488877.6:c.690G>A	ENSP00000425159.1:n.690G>A
ENST00000492756.7:c.*228G>A	ENSP00000422453.1:n.*228G>A
ENST00000494799.6:c.82G>A	ENSP00000512834.1:p.Val28Ile
ENST00000562983.3:c.82G>A	ENSP00000512845.1:p.Val28Ile
ENST00000612663.6:c.*201G>A	ENSP00000477997.3:n.*201G>A
ENST00000640140.2:n.944G>A
ENST00000640250.2:n.298G>A
ENST00000640681.2:n.903G>A
ENST00000696723.1:n.4432G>A
ENST00000696741.1:n.2437G>A
ENST00000696742.1:n.2164G>A
ENST00000696743.1:n.3567G>A
ENST00000696744.1:n.838G>A
ENST00000696767.1:n.1133G>A
ENST00000696768.1:c.*122G>A	ENSP00000512859.1:n.*122G>A
ENST00000696769.1:n.2488G>A
ENST00000696771.1:c.82G>A	ENSP00000512860.1:p.Val28Ile
ENST00000696772.1:n.2402G>A
ENST00000696773.1:n.2141G>A
ENST00000696774.1:n.5909G>A
ENST00000696776.1:c.892G>A	ENSP00000512861.1:p.Val298Ile
ENST00000696777.1:n.2207G>A
ENST00000696778.1:n.1235G>A
ENST00000696779.1:c.406G>A	ENSP00000512862.1:p.Val136Ile
ENST00000696780.1:c.829G>A	ENSP00000512863.1:p.Val277Ile
ENST00000696781.1:c.544G>A	ENSP00000512864.1:p.Val182Ile
ENST00000696782.1:c.*201G>A	ENSP00000512865.1:n.*201G>A
ENST00000696783.1:n.2667G>A
ENST00000696992.1:n.1916G>A
ENST00000696995.1:n.4328G>A
ENST00000696996.1:n.2241G>A
ENST00000696997.1:c.*429G>A	ENSP00000513028.1:n.*429G>A
ENST00000696998.1:n.2053G>A
ENST00000696999.1:c.82G>A	ENSP00000513029.1:p.Val28Ile
ENST00000697035.1:c.*132G>A	ENSP00000513059.1:n.*132G>A
ENST00000697036.1:c.*215G>A	ENSP00000513060.1:n.*215G>A
ENST00000697037.1:n.834G>A
ENST00000697093.1:n.3035G>A
ENST00000697094.1:n.3382G>A
ENST00000697095.1:c.*2000G>A	ENSP00000513104.1:n.*2000G>A
ENST00000697096.1:n.1932G>A
ENST00000697097.1:c.82G>A	ENSP00000513105.1:p.Val28Ile
ENST00000562983.2:n.985G>A
ENST00000690268.1:c.880G>A	ENSP00000509810.1:p.Val294Ile
ENST00000355740.7:c.*125G>A	ENSP00000347979.3:n.*125G>A
ENST00000612663.5:c.*201G>A	ENSP00000477997.3:n.*201G>A
ENST00000640140.1:n.971G>A
ENST00000640250.1:n.298G>A
ENST00000640681.1:n.920G>A
ENST00000652046.1:c.799G>A MANE Select	ENSP00000498466.1:p.Val267Ile
ENST00000352159.8:c.*116G>A	ENSP00000345601.4:n.*116G>A
ENST00000355279.2:c.774G>A	ENSP00000347426.2:n.774G>A
ENST00000355740.6:c.799G>A	ENSP00000347979.2:p.Val267Ile
ENST00000357339.6:c.736G>A	ENSP00000349896.2:p.Val246Ile
ENST00000479522.5:c.*228G>A	ENSP00000424113.1:n.*228G>A
ENST00000484444.5:c.*240G>A	ENSP00000420975.1:n.*240G>A
ENST00000488877.5:c.*240G>A	ENSP00000425159.1:n.*240G>A
ENST00000492756.5:c.627G>A	ENSP00000422453.1:n.627G>A
ENST00000494410.5:c.*157G>A	ENSP00000423755.1:n.*157G>A
ENST00000612663.4:c.*146G>A	ENSP00000477997.2:n.*146G>A
NM_000043.4:c.799G>A , LRG_134t1:c.799G>A	NP_000034.1:p.Val267Ile
NM_152871.2:c.736G>A	NP_690610.1:p.Val246Ile
NM_152872.2:c.*111G>A	NP_690611.1:n.*111G>A
NR_028033.2:n.973G>A
NR_028034.2:n.835G>A
NR_028035.2:n.898G>A
NR_028036.2:n.1036G>A
XM_006717819.2:c.880G>A	XP_006717882.1:p.Val294Ile
XM_011539764.1:c.961G>A	XP_011538066.1:p.Val321Ile
XM_011539765.1:c.898G>A	XP_011538067.1:p.Val300Ile
XM_011539766.1:c.880G>A	XP_011538068.1:p.Val294Ile
XM_011539767.1:c.844G>A	XP_011538069.1:p.Val282Ile
XR_945732.1:n.867G>A
XR_945733.1:n.804G>A
NM_000043.5:c.799G>A	NP_000034.1:p.Val267Ile
NM_001320619.1:c.*122G>A	NP_001307548.1:n.*122G>A
NM_152871.3:c.736G>A	NP_690610.1:p.Val246Ile
NM_152872.3:c.*111G>A	NP_690611.1:n.*111G>A
NR_028033.3:n.945G>A
NR_028034.3:n.807G>A
NR_028035.3:n.870G>A
NR_028036.3:n.1008G>A
NR_135313.1:n.925G>A
NR_135314.1:n.1108G>A
NR_135315.1:n.861G>A
XM_006717819.3:c.880G>A	XP_006717882.1:p.Val294Ile
XM_011539764.2:c.961G>A	XP_011538066.1:p.Val321Ile
XM_011539765.2:c.898G>A	XP_011538067.1:p.Val300Ile
XM_011539766.2:c.880G>A	XP_011538068.1:p.Val294Ile
XM_011539767.3:c.844G>A	XP_011538069.1:p.Val282Ile
XR_945732.3:n.867G>A
XR_945733.2:n.804G>A
NM_000043.6:c.799G>A MANE Select	NP_000034.1:p.Val267Ile
NM_001320619.2:c.*122G>A	NP_001307548.1:n.*122G>A
NM_152871.4:c.736G>A	NP_690610.1:p.Val246Ile
NM_152872.4:c.*111G>A	NP_690611.1:n.*111G>A
NR_028033.4:n.706G>A
NR_028034.4:n.568G>A
NR_028035.4:n.631G>A
NR_028036.4:n.769G>A
NR_135313.2:n.686G>A
NR_135314.2:n.965G>A
NR_135315.2:n.718G>A