Canonical Allele Identifier: CA5593266

Gene: FAS

Linked Data

• dbSNP Id: rs748567150
• ExAC: 10:90774395 G / T
• gnomAD v2: 10-90774395-G-T
• gnomAD v4: 10-89014638-G-T
• MyVariant Identifiers: chr10:g.90774395G>T (hg19) ; chr10:g.89014638G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014638G>T , CM000672.2:g.89014638G>T	GRCh38
NC_000010.10:g.90774395G>T , CM000672.1:g.90774395G>T	GRCh37
NC_000010.9:g.90764375G>T	NCBI36
NG_009089.2:g.29108G>T , LRG_134:g.29108G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1505G>T
ENST00000355740.8:c.*519G>T	ENSP00000347979.3:n.*519G>T
ENST00000357339.7:c.*188G>T	ENSP00000349896.2:n.*188G>T
ENST00000371857.8:n.2741G>T
ENST00000460510.6:c.*188G>T	ENSP00000512812.1:n.*188G>T
ENST00000466081.6:n.2845G>T
ENST00000477270.6:c.*188G>T	ENSP00000512813.1:n.*188G>T
ENST00000488877.6:c.1087G>T	ENSP00000425159.1:n.1087G>T
ENST00000492756.7:c.*625G>T	ENSP00000422453.1:n.*625G>T
ENST00000494799.6:c.*188G>T	ENSP00000512834.1:n.*188G>T
ENST00000562983.3:c.*188G>T	ENSP00000512845.1:n.*188G>T
ENST00000612663.6:c.*598G>T	ENSP00000477997.3:n.*598G>T
ENST00000640140.2:n.1341G>T
ENST00000640250.2:n.695G>T
ENST00000640681.2:n.1300G>T
ENST00000696723.1:n.4829G>T
ENST00000696741.1:n.2834G>T
ENST00000696742.1:n.2561G>T
ENST00000696743.1:n.3964G>T
ENST00000696744.1:n.1235G>T
ENST00000696767.1:n.1530G>T
ENST00000696768.1:c.*519G>T	ENSP00000512859.1:n.*519G>T
ENST00000696771.1:c.*188G>T	ENSP00000512860.1:n.*188G>T
ENST00000696772.1:n.2799G>T
ENST00000696773.1:n.2538G>T
ENST00000696774.1:n.6306G>T
ENST00000696776.1:c.*188G>T	ENSP00000512861.1:n.*188G>T
ENST00000696777.1:n.2604G>T
ENST00000696778.1:n.1632G>T
ENST00000696779.1:c.*188G>T	ENSP00000512862.1:n.*188G>T
ENST00000696780.1:c.*188G>T	ENSP00000512863.1:n.*188G>T
ENST00000696781.1:c.*188G>T	ENSP00000512864.1:n.*188G>T
ENST00000696782.1:c.*598G>T	ENSP00000512865.1:n.*598G>T
ENST00000696783.1:n.3064G>T
ENST00000696992.1:n.2313G>T
ENST00000696995.1:n.4725G>T
ENST00000696996.1:n.2638G>T
ENST00000696997.1:c.*826G>T	ENSP00000513028.1:n.*826G>T
ENST00000696998.1:n.2450G>T
ENST00000696999.1:c.*188G>T	ENSP00000513029.1:n.*188G>T
ENST00000697036.1:c.*612G>T	ENSP00000513060.1:n.*612G>T
ENST00000697037.1:n.1231G>T
ENST00000697093.1:n.3432G>T
ENST00000697094.1:n.3779G>T
ENST00000697095.1:c.*2397G>T	ENSP00000513104.1:n.*2397G>T
ENST00000697096.1:n.2329G>T
ENST00000697097.1:c.*188G>T	ENSP00000513105.1:n.*188G>T
ENST00000562983.2:n.1382G>T
ENST00000690268.1:c.*188G>T	ENSP00000509810.1:n.*188G>T
ENST00000355740.7:c.*522G>T	ENSP00000347979.3:n.*522G>T
ENST00000640140.1:n.1368G>T
ENST00000640250.1:n.695G>T
ENST00000640681.1:n.1317G>T
ENST00000652046.1:c.*188G>T MANE Select	ENSP00000498466.1:n.*188G>T
ENST00000352159.8:c.*513G>T	ENSP00000345601.4:n.*513G>T
ENST00000355740.6:c.*188G>T	ENSP00000347979.2:n.*188G>T
NM_000043.4:c.*188G>T , LRG_134t1:c.*188G>T	NP_000034.1:n.*188G>T
NM_152871.2:c.*188G>T	NP_690610.1:n.*188G>T
NM_152872.2:c.*508G>T	NP_690611.1:n.*508G>T
NR_028033.2:n.1370G>T
NR_028034.2:n.1232G>T
NR_028035.2:n.1295G>T
NR_028036.2:n.1433G>T
XM_006717819.2:c.*188G>T	XP_006717882.1:n.*188G>T
XM_011539764.1:c.*188G>T	XP_011538066.1:n.*188G>T
XM_011539765.1:c.*188G>T	XP_011538067.1:n.*188G>T
XM_011539766.1:c.*188G>T	XP_011538068.1:n.*188G>T
XM_011539767.1:c.*188G>T	XP_011538069.1:n.*188G>T
NM_000043.5:c.*188G>T	NP_000034.1:n.*188G>T
NM_001320619.1:c.*519G>T	NP_001307548.1:n.*519G>T
NM_152871.3:c.*188G>T	NP_690610.1:n.*188G>T
NM_152872.3:c.*508G>T	NP_690611.1:n.*508G>T
NR_028033.3:n.1342G>T
NR_028034.3:n.1204G>T
NR_028035.3:n.1267G>T
NR_028036.3:n.1405G>T
NR_135313.1:n.1322G>T
NR_135314.1:n.1505G>T
NR_135315.1:n.1258G>T
XM_006717819.3:c.*188G>T	XP_006717882.1:n.*188G>T
XM_011539764.2:c.*188G>T	XP_011538066.1:n.*188G>T
XM_011539765.2:c.*188G>T	XP_011538067.1:n.*188G>T
XM_011539766.2:c.*188G>T	XP_011538068.1:n.*188G>T
XM_011539767.3:c.*188G>T	XP_011538069.1:n.*188G>T
XR_945732.3:n.1264G>T
XR_945733.2:n.1201G>T
NM_000043.6:c.*188G>T MANE Select	NP_000034.1:n.*188G>T
NM_001320619.2:c.*519G>T	NP_001307548.1:n.*519G>T
NM_152871.4:c.*188G>T	NP_690610.1:n.*188G>T
NM_152872.4:c.*508G>T	NP_690611.1:n.*508G>T
NR_028033.4:n.1103G>T
NR_028034.4:n.965G>T
NR_028035.4:n.1028G>T
NR_028036.4:n.1166G>T
NR_135313.2:n.1083G>T
NR_135314.2:n.1362G>T
NR_135315.2:n.1115G>T