Canonical Allele Identifier: CA470974958

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774132G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014375G>A , CM000672.2:g.89014375G>A	GRCh38
NC_000010.10:g.90774132G>A , CM000672.1:g.90774132G>A	GRCh37
NC_000010.9:g.90764112G>A	NCBI36
NG_009089.2:g.28845G>A , LRG_134:g.28845G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1242G>A
ENST00000355740.8:c.*256G>A	ENSP00000347979.3:n.*256G>A
ENST00000357339.7:c.870G>A	ENSP00000349896.2:p.Gln290=
ENST00000371857.8:n.2478G>A
ENST00000460510.6:c.216G>A	ENSP00000512812.1:p.Gln72=
ENST00000466081.6:n.2582G>A
ENST00000477270.6:c.978G>A	ENSP00000512813.1:p.Gln326=
ENST00000479522.6:c.*362G>A	ENSP00000424113.1:n.*362G>A
ENST00000484444.6:c.*374G>A	ENSP00000420975.1:n.*374G>A
ENST00000488877.6:c.824G>A	ENSP00000425159.1:n.824G>A
ENST00000492756.7:c.*362G>A	ENSP00000422453.1:n.*362G>A
ENST00000494799.6:c.216G>A	ENSP00000512834.1:p.Gln72=
ENST00000562983.3:c.216G>A	ENSP00000512845.1:p.Gln72=
ENST00000612663.6:c.*335G>A	ENSP00000477997.3:n.*335G>A
ENST00000640140.2:n.1078G>A
ENST00000640250.2:n.432G>A
ENST00000640681.2:n.1037G>A
ENST00000696723.1:n.4566G>A
ENST00000696741.1:n.2571G>A
ENST00000696742.1:n.2298G>A
ENST00000696743.1:n.3701G>A
ENST00000696744.1:n.972G>A
ENST00000696767.1:n.1267G>A
ENST00000696768.1:c.*256G>A	ENSP00000512859.1:n.*256G>A
ENST00000696769.1:n.2622G>A
ENST00000696771.1:c.216G>A	ENSP00000512860.1:p.Gln72=
ENST00000696772.1:n.2536G>A
ENST00000696773.1:n.2275G>A
ENST00000696774.1:n.6043G>A
ENST00000696776.1:c.1026G>A	ENSP00000512861.1:p.Gln342=
ENST00000696777.1:n.2341G>A
ENST00000696778.1:n.1369G>A
ENST00000696779.1:c.540G>A	ENSP00000512862.1:p.Gln180=
ENST00000696780.1:c.963G>A	ENSP00000512863.1:p.Gln321=
ENST00000696781.1:c.678G>A	ENSP00000512864.1:p.Gln226=
ENST00000696782.1:c.*335G>A	ENSP00000512865.1:n.*335G>A
ENST00000696783.1:n.2801G>A
ENST00000696992.1:n.2050G>A
ENST00000696995.1:n.4462G>A
ENST00000696996.1:n.2375G>A
ENST00000696997.1:c.*563G>A	ENSP00000513028.1:n.*563G>A
ENST00000696998.1:n.2187G>A
ENST00000696999.1:c.216G>A	ENSP00000513029.1:p.Gln72=
ENST00000697036.1:c.*349G>A	ENSP00000513060.1:n.*349G>A
ENST00000697037.1:n.968G>A
ENST00000697093.1:n.3169G>A
ENST00000697094.1:n.3516G>A
ENST00000697095.1:c.*2134G>A	ENSP00000513104.1:n.*2134G>A
ENST00000697096.1:n.2066G>A
ENST00000697097.1:c.216G>A	ENSP00000513105.1:p.Gln72=
ENST00000562983.2:n.1119G>A
ENST00000690268.1:c.1014G>A	ENSP00000509810.1:p.Gln338=
ENST00000355740.7:c.*259G>A	ENSP00000347979.3:n.*259G>A
ENST00000612663.5:c.*335G>A	ENSP00000477997.3:n.*335G>A
ENST00000640140.1:n.1105G>A
ENST00000640250.1:n.432G>A
ENST00000640681.1:n.1054G>A
ENST00000652046.1:c.933G>A MANE Select	ENSP00000498466.1:p.Gln311=
ENST00000352159.8:c.*250G>A	ENSP00000345601.4:n.*250G>A
ENST00000355279.2:c.908G>A	ENSP00000347426.2:n.908G>A
ENST00000355740.6:c.933G>A	ENSP00000347979.2:p.Gln311=
ENST00000357339.6:c.870G>A	ENSP00000349896.2:p.Gln290=
ENST00000479522.5:c.*362G>A	ENSP00000424113.1:n.*362G>A
ENST00000484444.5:c.*374G>A	ENSP00000420975.1:n.*374G>A
ENST00000488877.5:c.*374G>A	ENSP00000425159.1:n.*374G>A
ENST00000492756.5:c.761G>A	ENSP00000422453.1:n.761G>A
ENST00000494410.5:c.*291G>A	ENSP00000423755.1:n.*291G>A
ENST00000612663.4:c.*280G>A	ENSP00000477997.2:n.*280G>A
NM_000043.4:c.933G>A , LRG_134t1:c.933G>A	NP_000034.1:p.Gln311=
NM_152871.2:c.870G>A	NP_690610.1:p.Gln290=
NM_152872.2:c.*245G>A	NP_690611.1:n.*245G>A
NR_028033.2:n.1107G>A
NR_028034.2:n.969G>A
NR_028035.2:n.1032G>A
NR_028036.2:n.1170G>A
XM_006717819.2:c.1014G>A	XP_006717882.1:p.Gln338=
XM_011539764.1:c.1095G>A	XP_011538066.1:p.Gln365=
XM_011539765.1:c.1032G>A	XP_011538067.1:p.Gln344=
XM_011539766.1:c.1014G>A	XP_011538068.1:p.Gln338=
XM_011539767.1:c.978G>A	XP_011538069.1:p.Gln326=
XR_945733.1:n.938G>A
NM_000043.5:c.933G>A	NP_000034.1:p.Gln311=
NM_001320619.1:c.*256G>A	NP_001307548.1:n.*256G>A
NM_152871.3:c.870G>A	NP_690610.1:p.Gln290=
NM_152872.3:c.*245G>A	NP_690611.1:n.*245G>A
NR_028033.3:n.1079G>A
NR_028034.3:n.941G>A
NR_028035.3:n.1004G>A
NR_028036.3:n.1142G>A
NR_135313.1:n.1059G>A
NR_135314.1:n.1242G>A
NR_135315.1:n.995G>A
XM_006717819.3:c.1014G>A	XP_006717882.1:p.Gln338=
XM_011539764.2:c.1095G>A	XP_011538066.1:p.Gln365=
XM_011539765.2:c.1032G>A	XP_011538067.1:p.Gln344=
XM_011539766.2:c.1014G>A	XP_011538068.1:p.Gln338=
XM_011539767.3:c.978G>A	XP_011538069.1:p.Gln326=
XR_945732.3:n.1001G>A
XR_945733.2:n.938G>A
NM_000043.6:c.933G>A MANE Select	NP_000034.1:p.Gln311=
NM_001320619.2:c.*256G>A	NP_001307548.1:n.*256G>A
NM_152871.4:c.870G>A	NP_690610.1:p.Gln290=
NM_152872.4:c.*245G>A	NP_690611.1:n.*245G>A
NR_028033.4:n.840G>A
NR_028034.4:n.702G>A
NR_028035.4:n.765G>A
NR_028036.4:n.903G>A
NR_135313.2:n.820G>A
NR_135314.2:n.1099G>A
NR_135315.2:n.852G>A