Canonical Allele Identifier: CA377510164

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774143T>A (hg19) ; chr10:g.89014386T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014386T>A , CM000672.2:g.89014386T>A	GRCh38
NC_000010.10:g.90774143T>A , CM000672.1:g.90774143T>A	GRCh37
NC_000010.9:g.90764123T>A	NCBI36
NG_009089.2:g.28856T>A , LRG_134:g.28856T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1253T>A
ENST00000355740.8:c.*267T>A	ENSP00000347979.3:n.*267T>A
ENST00000357339.7:c.881T>A	ENSP00000349896.2:p.Leu294His
ENST00000371857.8:n.2489T>A
ENST00000460510.6:c.227T>A	ENSP00000512812.1:p.Leu76His
ENST00000466081.6:n.2593T>A
ENST00000477270.6:c.989T>A	ENSP00000512813.1:p.Leu330His
ENST00000479522.6:c.*373T>A	ENSP00000424113.1:n.*373T>A
ENST00000484444.6:c.*385T>A	ENSP00000420975.1:n.*385T>A
ENST00000488877.6:c.835T>A	ENSP00000425159.1:n.835T>A
ENST00000492756.7:c.*373T>A	ENSP00000422453.1:n.*373T>A
ENST00000494799.6:c.227T>A	ENSP00000512834.1:p.Leu76His
ENST00000562983.3:c.227T>A	ENSP00000512845.1:p.Leu76His
ENST00000612663.6:c.*346T>A	ENSP00000477997.3:n.*346T>A
ENST00000640140.2:n.1089T>A
ENST00000640250.2:n.443T>A
ENST00000640681.2:n.1048T>A
ENST00000696723.1:n.4577T>A
ENST00000696741.1:n.2582T>A
ENST00000696742.1:n.2309T>A
ENST00000696743.1:n.3712T>A
ENST00000696744.1:n.983T>A
ENST00000696767.1:n.1278T>A
ENST00000696768.1:c.*267T>A	ENSP00000512859.1:n.*267T>A
ENST00000696769.1:n.2633T>A
ENST00000696771.1:c.227T>A	ENSP00000512860.1:p.Leu76His
ENST00000696772.1:n.2547T>A
ENST00000696773.1:n.2286T>A
ENST00000696774.1:n.6054T>A
ENST00000696776.1:c.1037T>A	ENSP00000512861.1:p.Leu346His
ENST00000696777.1:n.2352T>A
ENST00000696778.1:n.1380T>A
ENST00000696779.1:c.551T>A	ENSP00000512862.1:p.Leu184His
ENST00000696780.1:c.974T>A	ENSP00000512863.1:p.Leu325His
ENST00000696781.1:c.689T>A	ENSP00000512864.1:p.Leu230His
ENST00000696782.1:c.*346T>A	ENSP00000512865.1:n.*346T>A
ENST00000696783.1:n.2812T>A
ENST00000696992.1:n.2061T>A
ENST00000696995.1:n.4473T>A
ENST00000696996.1:n.2386T>A
ENST00000696997.1:c.*574T>A	ENSP00000513028.1:n.*574T>A
ENST00000696998.1:n.2198T>A
ENST00000696999.1:c.227T>A	ENSP00000513029.1:p.Leu76His
ENST00000697036.1:c.*360T>A	ENSP00000513060.1:n.*360T>A
ENST00000697037.1:n.979T>A
ENST00000697093.1:n.3180T>A
ENST00000697094.1:n.3527T>A
ENST00000697095.1:c.*2145T>A	ENSP00000513104.1:n.*2145T>A
ENST00000697096.1:n.2077T>A
ENST00000697097.1:c.227T>A	ENSP00000513105.1:p.Leu76His
ENST00000562983.2:n.1130T>A
ENST00000690268.1:c.1025T>A	ENSP00000509810.1:p.Leu342His
ENST00000355740.7:c.*270T>A	ENSP00000347979.3:n.*270T>A
ENST00000612663.5:c.*346T>A	ENSP00000477997.3:n.*346T>A
ENST00000640140.1:n.1116T>A
ENST00000640250.1:n.443T>A
ENST00000640681.1:n.1065T>A
ENST00000652046.1:c.944T>A MANE Select	ENSP00000498466.1:p.Leu315His
ENST00000352159.8:c.*261T>A	ENSP00000345601.4:n.*261T>A
ENST00000355279.2:c.919T>A	ENSP00000347426.2:n.919T>A
ENST00000355740.6:c.944T>A	ENSP00000347979.2:p.Leu315His
ENST00000357339.6:c.881T>A	ENSP00000349896.2:p.Leu294His
ENST00000479522.5:c.*373T>A	ENSP00000424113.1:n.*373T>A
ENST00000484444.5:c.*385T>A	ENSP00000420975.1:n.*385T>A
ENST00000488877.5:c.*385T>A	ENSP00000425159.1:n.*385T>A
ENST00000492756.5:c.772T>A	ENSP00000422453.1:n.772T>A
ENST00000494410.5:c.*302T>A	ENSP00000423755.1:n.*302T>A
ENST00000612663.4:c.*291T>A	ENSP00000477997.2:n.*291T>A
NM_000043.4:c.944T>A , LRG_134t1:c.944T>A	NP_000034.1:p.Leu315His
NM_152871.2:c.881T>A	NP_690610.1:p.Leu294His
NM_152872.2:c.*256T>A	NP_690611.1:n.*256T>A
NR_028033.2:n.1118T>A
NR_028034.2:n.980T>A
NR_028035.2:n.1043T>A
NR_028036.2:n.1181T>A
XM_006717819.2:c.1025T>A	XP_006717882.1:p.Leu342His
XM_011539764.1:c.1106T>A	XP_011538066.1:p.Leu369His
XM_011539765.1:c.1043T>A	XP_011538067.1:p.Leu348His
XM_011539766.1:c.1025T>A	XP_011538068.1:p.Leu342His
XM_011539767.1:c.989T>A	XP_011538069.1:p.Leu330His
XR_945733.1:n.949T>A
NM_000043.5:c.944T>A	NP_000034.1:p.Leu315His
NM_001320619.1:c.*267T>A	NP_001307548.1:n.*267T>A
NM_152871.3:c.881T>A	NP_690610.1:p.Leu294His
NM_152872.3:c.*256T>A	NP_690611.1:n.*256T>A
NR_028033.3:n.1090T>A
NR_028034.3:n.952T>A
NR_028035.3:n.1015T>A
NR_028036.3:n.1153T>A
NR_135313.1:n.1070T>A
NR_135314.1:n.1253T>A
NR_135315.1:n.1006T>A
XM_006717819.3:c.1025T>A	XP_006717882.1:p.Leu342His
XM_011539764.2:c.1106T>A	XP_011538066.1:p.Leu369His
XM_011539765.2:c.1043T>A	XP_011538067.1:p.Leu348His
XM_011539766.2:c.1025T>A	XP_011538068.1:p.Leu342His
XM_011539767.3:c.989T>A	XP_011538069.1:p.Leu330His
XR_945732.3:n.1012T>A
XR_945733.2:n.949T>A
NM_000043.6:c.944T>A MANE Select	NP_000034.1:p.Leu315His
NM_001320619.2:c.*267T>A	NP_001307548.1:n.*267T>A
NM_152871.4:c.881T>A	NP_690610.1:p.Leu294His
NM_152872.4:c.*256T>A	NP_690611.1:n.*256T>A
NR_028033.4:n.851T>A
NR_028034.4:n.713T>A
NR_028035.4:n.776T>A
NR_028036.4:n.914T>A
NR_135313.2:n.831T>A
NR_135314.2:n.1110T>A
NR_135315.2:n.863T>A