Canonical Allele Identifier: CA377509719

Gene: FAS

Linked Data

• dbSNP Id: rs114658485
• gnomAD v4: 10-89014195-G-T
• MyVariant Identifiers: chr10:g.90773952G>T (hg19) ; chr10:g.89014195G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014195G>T , CM000672.2:g.89014195G>T	GRCh38
NC_000010.10:g.90773952G>T , CM000672.1:g.90773952G>T	GRCh37
NC_000010.9:g.90763932G>T	NCBI36
NG_009089.2:g.28665G>T , LRG_134:g.28665G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1062G>T
ENST00000355740.8:c.*76G>T	ENSP00000347979.3:n.*76G>T
ENST00000357339.7:c.690G>T	ENSP00000349896.2:p.Lys230Asn
ENST00000371857.8:n.2298G>T
ENST00000460510.6:c.36G>T	ENSP00000512812.1:p.Lys12Asn
ENST00000466081.6:n.2402G>T
ENST00000477270.6:c.798G>T	ENSP00000512813.1:p.Lys266Asn
ENST00000479522.6:c.*182G>T	ENSP00000424113.1:n.*182G>T
ENST00000484444.6:c.*194G>T	ENSP00000420975.1:n.*194G>T
ENST00000488877.6:c.644G>T	ENSP00000425159.1:n.644G>T
ENST00000492756.7:c.*182G>T	ENSP00000422453.1:n.*182G>T
ENST00000494799.6:c.36G>T	ENSP00000512834.1:p.Lys12Asn
ENST00000562983.3:c.36G>T	ENSP00000512845.1:p.Lys12Asn
ENST00000612663.6:c.*155G>T	ENSP00000477997.3:n.*155G>T
ENST00000640140.2:n.898G>T
ENST00000640250.2:n.252G>T
ENST00000640681.2:n.857G>T
ENST00000696723.1:n.4386G>T
ENST00000696741.1:n.2391G>T
ENST00000696742.1:n.2118G>T
ENST00000696743.1:n.3521G>T
ENST00000696744.1:n.792G>T
ENST00000696767.1:n.1087G>T
ENST00000696768.1:c.*76G>T	ENSP00000512859.1:n.*76G>T
ENST00000696769.1:n.2442G>T
ENST00000696771.1:c.36G>T	ENSP00000512860.1:p.Lys12Asn
ENST00000696772.1:n.2356G>T
ENST00000696773.1:n.2095G>T
ENST00000696774.1:n.5863G>T
ENST00000696776.1:c.846G>T	ENSP00000512861.1:p.Lys282Asn
ENST00000696777.1:n.2161G>T
ENST00000696778.1:n.1189G>T
ENST00000696779.1:c.360G>T	ENSP00000512862.1:p.Lys120Asn
ENST00000696780.1:c.783G>T	ENSP00000512863.1:p.Lys261Asn
ENST00000696781.1:c.498G>T	ENSP00000512864.1:p.Lys166Asn
ENST00000696782.1:c.*155G>T	ENSP00000512865.1:n.*155G>T
ENST00000696783.1:n.2621G>T
ENST00000696992.1:n.1870G>T
ENST00000696995.1:n.4282G>T
ENST00000696996.1:n.2195G>T
ENST00000696997.1:c.*383G>T	ENSP00000513028.1:n.*383G>T
ENST00000696998.1:n.2007G>T
ENST00000696999.1:c.36G>T	ENSP00000513029.1:p.Lys12Asn
ENST00000697035.1:c.*86G>T	ENSP00000513059.1:n.*86G>T
ENST00000697036.1:c.*169G>T	ENSP00000513060.1:n.*169G>T
ENST00000697037.1:n.788G>T
ENST00000697093.1:n.2989G>T
ENST00000697094.1:n.3336G>T
ENST00000697095.1:c.*1954G>T	ENSP00000513104.1:n.*1954G>T
ENST00000697096.1:n.1886G>T
ENST00000697097.1:c.36G>T	ENSP00000513105.1:p.Lys12Asn
ENST00000562983.2:n.939G>T
ENST00000690268.1:c.834G>T	ENSP00000509810.1:p.Lys278Asn
ENST00000355740.7:c.*79G>T	ENSP00000347979.3:n.*79G>T
ENST00000612663.5:c.*155G>T	ENSP00000477997.3:n.*155G>T
ENST00000640140.1:n.925G>T
ENST00000640250.1:n.252G>T
ENST00000640681.1:n.874G>T
ENST00000652046.1:c.753G>T MANE Select	ENSP00000498466.1:p.Lys251Asn
ENST00000352159.8:c.*70G>T	ENSP00000345601.4:n.*70G>T
ENST00000355279.2:c.728G>T	ENSP00000347426.2:n.728G>T
ENST00000355740.6:c.753G>T	ENSP00000347979.2:p.Lys251Asn
ENST00000357339.6:c.690G>T	ENSP00000349896.2:p.Lys230Asn
ENST00000479522.5:c.*182G>T	ENSP00000424113.1:n.*182G>T
ENST00000484444.5:c.*194G>T	ENSP00000420975.1:n.*194G>T
ENST00000488877.5:c.*194G>T	ENSP00000425159.1:n.*194G>T
ENST00000492756.5:c.581G>T	ENSP00000422453.1:n.581G>T
ENST00000494410.5:c.*111G>T	ENSP00000423755.1:n.*111G>T
ENST00000494799.5:n.660G>T
ENST00000612663.4:c.*100G>T	ENSP00000477997.2:n.*100G>T
ENST00000615406.4:c.751G>T	ENSP00000484575.1:p.Glu251Ter
NM_000043.4:c.753G>T , LRG_134t1:c.753G>T	NP_000034.1:p.Lys251Asn
NM_152871.2:c.690G>T	NP_690610.1:p.Lys230Asn
NM_152872.2:c.*65G>T	NP_690611.1:n.*65G>T
NR_028033.2:n.927G>T
NR_028034.2:n.789G>T
NR_028035.2:n.852G>T
NR_028036.2:n.990G>T
XM_006717819.2:c.834G>T	XP_006717882.1:p.Lys278Asn
XM_011539764.1:c.915G>T	XP_011538066.1:p.Lys305Asn
XM_011539765.1:c.852G>T	XP_011538067.1:p.Lys284Asn
XM_011539766.1:c.834G>T	XP_011538068.1:p.Lys278Asn
XM_011539767.1:c.798G>T	XP_011538069.1:p.Lys266Asn
XR_945732.1:n.821G>T
XR_945733.1:n.758G>T
NM_000043.5:c.753G>T	NP_000034.1:p.Lys251Asn
NM_001320619.1:c.*76G>T	NP_001307548.1:n.*76G>T
NM_152871.3:c.690G>T	NP_690610.1:p.Lys230Asn
NM_152872.3:c.*65G>T	NP_690611.1:n.*65G>T
NR_028033.3:n.899G>T
NR_028034.3:n.761G>T
NR_028035.3:n.824G>T
NR_028036.3:n.962G>T
NR_135313.1:n.879G>T
NR_135314.1:n.1062G>T
NR_135315.1:n.815G>T
XM_006717819.3:c.834G>T	XP_006717882.1:p.Lys278Asn
XM_011539764.2:c.915G>T	XP_011538066.1:p.Lys305Asn
XM_011539765.2:c.852G>T	XP_011538067.1:p.Lys284Asn
XM_011539766.2:c.834G>T	XP_011538068.1:p.Lys278Asn
XM_011539767.3:c.798G>T	XP_011538069.1:p.Lys266Asn
XR_945732.3:n.821G>T
XR_945733.2:n.758G>T
NM_000043.6:c.753G>T MANE Select	NP_000034.1:p.Lys251Asn
NM_001320619.2:c.*76G>T	NP_001307548.1:n.*76G>T
NM_152871.4:c.690G>T	NP_690610.1:p.Lys230Asn
NM_152872.4:c.*65G>T	NP_690611.1:n.*65G>T
NR_028033.4:n.660G>T
NR_028034.4:n.522G>T
NR_028035.4:n.585G>T
NR_028036.4:n.723G>T
NR_135313.2:n.640G>T
NR_135314.2:n.919G>T
NR_135315.2:n.672G>T