Canonical Allele Identifier: CA595185134

Gene: FAS

Linked Data

• dbSNP Id: rs1401121739
• gnomAD v2: 10-90774270-G-A
• MyVariant Identifiers: chr10:g.90774270G>A (hg19) ; chr10:g.89014513G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014513G>A , CM000672.2:g.89014513G>A	GRCh38
NC_000010.10:g.90774270G>A , CM000672.1:g.90774270G>A	GRCh37
NC_000010.9:g.90764250G>A	NCBI36
NG_009089.2:g.28983G>A , LRG_134:g.28983G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1380G>A
ENST00000355740.8:c.*394G>A	ENSP00000347979.3:n.*394G>A
ENST00000357339.7:c.*63G>A	ENSP00000349896.2:n.*63G>A
ENST00000371857.8:n.2616G>A
ENST00000460510.6:c.*63G>A	ENSP00000512812.1:n.*63G>A
ENST00000466081.6:n.2720G>A
ENST00000477270.6:c.*63G>A	ENSP00000512813.1:n.*63G>A
ENST00000479522.6:c.*500G>A	ENSP00000424113.1:n.*500G>A
ENST00000484444.6:c.*512G>A	ENSP00000420975.1:n.*512G>A
ENST00000488877.6:c.962G>A	ENSP00000425159.1:n.962G>A
ENST00000492756.7:c.*500G>A	ENSP00000422453.1:n.*500G>A
ENST00000494799.6:c.*63G>A	ENSP00000512834.1:n.*63G>A
ENST00000562983.3:c.*63G>A	ENSP00000512845.1:n.*63G>A
ENST00000612663.6:c.*473G>A	ENSP00000477997.3:n.*473G>A
ENST00000640140.2:n.1216G>A
ENST00000640250.2:n.570G>A
ENST00000640681.2:n.1175G>A
ENST00000696723.1:n.4704G>A
ENST00000696741.1:n.2709G>A
ENST00000696742.1:n.2436G>A
ENST00000696743.1:n.3839G>A
ENST00000696744.1:n.1110G>A
ENST00000696767.1:n.1405G>A
ENST00000696768.1:c.*394G>A	ENSP00000512859.1:n.*394G>A
ENST00000696769.1:n.2760G>A
ENST00000696771.1:c.*63G>A	ENSP00000512860.1:n.*63G>A
ENST00000696772.1:n.2674G>A
ENST00000696773.1:n.2413G>A
ENST00000696774.1:n.6181G>A
ENST00000696776.1:c.*63G>A	ENSP00000512861.1:n.*63G>A
ENST00000696777.1:n.2479G>A
ENST00000696778.1:n.1507G>A
ENST00000696779.1:c.*63G>A	ENSP00000512862.1:n.*63G>A
ENST00000696780.1:c.*63G>A	ENSP00000512863.1:n.*63G>A
ENST00000696781.1:c.*63G>A	ENSP00000512864.1:n.*63G>A
ENST00000696782.1:c.*473G>A	ENSP00000512865.1:n.*473G>A
ENST00000696783.1:n.2939G>A
ENST00000696992.1:n.2188G>A
ENST00000696995.1:n.4600G>A
ENST00000696996.1:n.2513G>A
ENST00000696997.1:c.*701G>A	ENSP00000513028.1:n.*701G>A
ENST00000696998.1:n.2325G>A
ENST00000696999.1:c.*63G>A	ENSP00000513029.1:n.*63G>A
ENST00000697036.1:c.*487G>A	ENSP00000513060.1:n.*487G>A
ENST00000697037.1:n.1106G>A
ENST00000697093.1:n.3307G>A
ENST00000697094.1:n.3654G>A
ENST00000697095.1:c.*2272G>A	ENSP00000513104.1:n.*2272G>A
ENST00000697096.1:n.2204G>A
ENST00000697097.1:c.*63G>A	ENSP00000513105.1:n.*63G>A
ENST00000562983.2:n.1257G>A
ENST00000690268.1:c.*63G>A	ENSP00000509810.1:n.*63G>A
ENST00000355740.7:c.*397G>A	ENSP00000347979.3:n.*397G>A
ENST00000640140.1:n.1243G>A
ENST00000640250.1:n.570G>A
ENST00000640681.1:n.1192G>A
ENST00000652046.1:c.*63G>A MANE Select	ENSP00000498466.1:n.*63G>A
ENST00000352159.8:c.*388G>A	ENSP00000345601.4:n.*388G>A
ENST00000355740.6:c.*63G>A	ENSP00000347979.2:n.*63G>A
ENST00000479522.5:c.*500G>A	ENSP00000424113.1:n.*500G>A
ENST00000484444.5:c.*512G>A	ENSP00000420975.1:n.*512G>A
ENST00000494410.5:c.*429G>A	ENSP00000423755.1:n.*429G>A
NM_000043.4:c.*63G>A , LRG_134t1:c.*63G>A	NP_000034.1:n.*63G>A
NM_152871.2:c.*63G>A	NP_690610.1:n.*63G>A
NM_152872.2:c.*383G>A	NP_690611.1:n.*383G>A
NR_028033.2:n.1245G>A
NR_028034.2:n.1107G>A
NR_028035.2:n.1170G>A
NR_028036.2:n.1308G>A
XM_006717819.2:c.*63G>A	XP_006717882.1:n.*63G>A
XM_011539764.1:c.*63G>A	XP_011538066.1:n.*63G>A
XM_011539765.1:c.*63G>A	XP_011538067.1:n.*63G>A
XM_011539766.1:c.*63G>A	XP_011538068.1:n.*63G>A
XM_011539767.1:c.*63G>A	XP_011538069.1:n.*63G>A
NM_000043.5:c.*63G>A	NP_000034.1:n.*63G>A
NM_001320619.1:c.*394G>A	NP_001307548.1:n.*394G>A
NM_152871.3:c.*63G>A	NP_690610.1:n.*63G>A
NM_152872.3:c.*383G>A	NP_690611.1:n.*383G>A
NR_028033.3:n.1217G>A
NR_028034.3:n.1079G>A
NR_028035.3:n.1142G>A
NR_028036.3:n.1280G>A
NR_135313.1:n.1197G>A
NR_135314.1:n.1380G>A
NR_135315.1:n.1133G>A
XM_006717819.3:c.*63G>A	XP_006717882.1:n.*63G>A
XM_011539764.2:c.*63G>A	XP_011538066.1:n.*63G>A
XM_011539765.2:c.*63G>A	XP_011538067.1:n.*63G>A
XM_011539766.2:c.*63G>A	XP_011538068.1:n.*63G>A
XM_011539767.3:c.*63G>A	XP_011538069.1:n.*63G>A
XR_945732.3:n.1139G>A
XR_945733.2:n.1076G>A
NM_000043.6:c.*63G>A MANE Select	NP_000034.1:n.*63G>A
NM_001320619.2:c.*394G>A	NP_001307548.1:n.*394G>A
NM_152871.4:c.*63G>A	NP_690610.1:n.*63G>A
NM_152872.4:c.*383G>A	NP_690611.1:n.*383G>A
NR_028033.4:n.978G>A
NR_028034.4:n.840G>A
NR_028035.4:n.903G>A
NR_028036.4:n.1041G>A
NR_135313.2:n.958G>A
NR_135314.2:n.1237G>A
NR_135315.2:n.990G>A