Canonical Allele Identifier: CA377510232

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774172T>A (hg19) ; chr10:g.89014415T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014415T>A , CM000672.2:g.89014415T>A	GRCh38
NC_000010.10:g.90774172T>A , CM000672.1:g.90774172T>A	GRCh37
NC_000010.9:g.90764152T>A	NCBI36
NG_009089.2:g.28885T>A , LRG_134:g.28885T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1282T>A
ENST00000355740.8:c.*296T>A	ENSP00000347979.3:n.*296T>A
ENST00000357339.7:c.910T>A	ENSP00000349896.2:p.Ser304Thr
ENST00000371857.8:n.2518T>A
ENST00000460510.6:c.256T>A	ENSP00000512812.1:p.Ser86Thr
ENST00000466081.6:n.2622T>A
ENST00000477270.6:c.1018T>A	ENSP00000512813.1:p.Ser340Thr
ENST00000479522.6:c.*402T>A	ENSP00000424113.1:n.*402T>A
ENST00000484444.6:c.*414T>A	ENSP00000420975.1:n.*414T>A
ENST00000488877.6:c.864T>A	ENSP00000425159.1:n.864T>A
ENST00000492756.7:c.*402T>A	ENSP00000422453.1:n.*402T>A
ENST00000494799.6:c.256T>A	ENSP00000512834.1:p.Ser86Thr
ENST00000562983.3:c.256T>A	ENSP00000512845.1:p.Ser86Thr
ENST00000612663.6:c.*375T>A	ENSP00000477997.3:n.*375T>A
ENST00000640140.2:n.1118T>A
ENST00000640250.2:n.472T>A
ENST00000640681.2:n.1077T>A
ENST00000696723.1:n.4606T>A
ENST00000696741.1:n.2611T>A
ENST00000696742.1:n.2338T>A
ENST00000696743.1:n.3741T>A
ENST00000696744.1:n.1012T>A
ENST00000696767.1:n.1307T>A
ENST00000696768.1:c.*296T>A	ENSP00000512859.1:n.*296T>A
ENST00000696769.1:n.2662T>A
ENST00000696771.1:c.256T>A	ENSP00000512860.1:p.Ser86Thr
ENST00000696772.1:n.2576T>A
ENST00000696773.1:n.2315T>A
ENST00000696774.1:n.6083T>A
ENST00000696776.1:c.1066T>A	ENSP00000512861.1:p.Ser356Thr
ENST00000696777.1:n.2381T>A
ENST00000696778.1:n.1409T>A
ENST00000696779.1:c.580T>A	ENSP00000512862.1:p.Ser194Thr
ENST00000696780.1:c.1003T>A	ENSP00000512863.1:p.Ser335Thr
ENST00000696781.1:c.718T>A	ENSP00000512864.1:p.Ser240Thr
ENST00000696782.1:c.*375T>A	ENSP00000512865.1:n.*375T>A
ENST00000696783.1:n.2841T>A
ENST00000696992.1:n.2090T>A
ENST00000696995.1:n.4502T>A
ENST00000696996.1:n.2415T>A
ENST00000696997.1:c.*603T>A	ENSP00000513028.1:n.*603T>A
ENST00000696998.1:n.2227T>A
ENST00000696999.1:c.256T>A	ENSP00000513029.1:p.Ser86Thr
ENST00000697036.1:c.*389T>A	ENSP00000513060.1:n.*389T>A
ENST00000697037.1:n.1008T>A
ENST00000697093.1:n.3209T>A
ENST00000697094.1:n.3556T>A
ENST00000697095.1:c.*2174T>A	ENSP00000513104.1:n.*2174T>A
ENST00000697096.1:n.2106T>A
ENST00000697097.1:c.256T>A	ENSP00000513105.1:p.Ser86Thr
ENST00000562983.2:n.1159T>A
ENST00000690268.1:c.1054T>A	ENSP00000509810.1:p.Ser352Thr
ENST00000355740.7:c.*299T>A	ENSP00000347979.3:n.*299T>A
ENST00000612663.5:c.*375T>A	ENSP00000477997.3:n.*375T>A
ENST00000640140.1:n.1145T>A
ENST00000640250.1:n.472T>A
ENST00000640681.1:n.1094T>A
ENST00000652046.1:c.973T>A MANE Select	ENSP00000498466.1:p.Ser325Thr
ENST00000352159.8:c.*290T>A	ENSP00000345601.4:n.*290T>A
ENST00000355279.2:c.948T>A	ENSP00000347426.2:n.948T>A
ENST00000355740.6:c.973T>A	ENSP00000347979.2:p.Ser325Thr
ENST00000357339.6:c.910T>A	ENSP00000349896.2:p.Ser304Thr
ENST00000479522.5:c.*402T>A	ENSP00000424113.1:n.*402T>A
ENST00000484444.5:c.*414T>A	ENSP00000420975.1:n.*414T>A
ENST00000488877.5:c.*414T>A	ENSP00000425159.1:n.*414T>A
ENST00000492756.5:c.801T>A	ENSP00000422453.1:n.801T>A
ENST00000494410.5:c.*331T>A	ENSP00000423755.1:n.*331T>A
ENST00000612663.4:c.*320T>A	ENSP00000477997.2:n.*320T>A
NM_000043.4:c.973T>A , LRG_134t1:c.973T>A	NP_000034.1:p.Ser325Thr
NM_152871.2:c.910T>A	NP_690610.1:p.Ser304Thr
NM_152872.2:c.*285T>A	NP_690611.1:n.*285T>A
NR_028033.2:n.1147T>A
NR_028034.2:n.1009T>A
NR_028035.2:n.1072T>A
NR_028036.2:n.1210T>A
XM_006717819.2:c.1054T>A	XP_006717882.1:p.Ser352Thr
XM_011539764.1:c.1135T>A	XP_011538066.1:p.Ser379Thr
XM_011539765.1:c.1072T>A	XP_011538067.1:p.Ser358Thr
XM_011539766.1:c.1054T>A	XP_011538068.1:p.Ser352Thr
XM_011539767.1:c.1018T>A	XP_011538069.1:p.Ser340Thr
XR_945733.1:n.978T>A
NM_000043.5:c.973T>A	NP_000034.1:p.Ser325Thr
NM_001320619.1:c.*296T>A	NP_001307548.1:n.*296T>A
NM_152871.3:c.910T>A	NP_690610.1:p.Ser304Thr
NM_152872.3:c.*285T>A	NP_690611.1:n.*285T>A
NR_028033.3:n.1119T>A
NR_028034.3:n.981T>A
NR_028035.3:n.1044T>A
NR_028036.3:n.1182T>A
NR_135313.1:n.1099T>A
NR_135314.1:n.1282T>A
NR_135315.1:n.1035T>A
XM_006717819.3:c.1054T>A	XP_006717882.1:p.Ser352Thr
XM_011539764.2:c.1135T>A	XP_011538066.1:p.Ser379Thr
XM_011539765.2:c.1072T>A	XP_011538067.1:p.Ser358Thr
XM_011539766.2:c.1054T>A	XP_011538068.1:p.Ser352Thr
XM_011539767.3:c.1018T>A	XP_011538069.1:p.Ser340Thr
XR_945732.3:n.1041T>A
XR_945733.2:n.978T>A
NM_000043.6:c.973T>A MANE Select	NP_000034.1:p.Ser325Thr
NM_001320619.2:c.*296T>A	NP_001307548.1:n.*296T>A
NM_152871.4:c.910T>A	NP_690610.1:p.Ser304Thr
NM_152872.4:c.*285T>A	NP_690611.1:n.*285T>A
NR_028033.4:n.880T>A
NR_028034.4:n.742T>A
NR_028035.4:n.805T>A
NR_028036.4:n.943T>A
NR_135313.2:n.860T>A
NR_135314.2:n.1139T>A
NR_135315.2:n.892T>A