Canonical Allele Identifier: CA377509749

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773963A>C (hg19) ; chr10:g.89014206A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014206A>C , CM000672.2:g.89014206A>C	GRCh38
NC_000010.10:g.90773963A>C , CM000672.1:g.90773963A>C	GRCh37
NC_000010.9:g.90763943A>C	NCBI36
NG_009089.2:g.28676A>C , LRG_134:g.28676A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1073A>C
ENST00000355740.8:c.*87A>C	ENSP00000347979.3:n.*87A>C
ENST00000357339.7:c.701A>C	ENSP00000349896.2:p.Asn234Thr
ENST00000371857.8:n.2309A>C
ENST00000460510.6:c.47A>C	ENSP00000512812.1:p.Asn16Thr
ENST00000466081.6:n.2413A>C
ENST00000477270.6:c.809A>C	ENSP00000512813.1:p.Asn270Thr
ENST00000479522.6:c.*193A>C	ENSP00000424113.1:n.*193A>C
ENST00000484444.6:c.*205A>C	ENSP00000420975.1:n.*205A>C
ENST00000488877.6:c.655A>C	ENSP00000425159.1:n.655A>C
ENST00000492756.7:c.*193A>C	ENSP00000422453.1:n.*193A>C
ENST00000494799.6:c.47A>C	ENSP00000512834.1:p.Asn16Thr
ENST00000562983.3:c.47A>C	ENSP00000512845.1:p.Asn16Thr
ENST00000612663.6:c.*166A>C	ENSP00000477997.3:n.*166A>C
ENST00000640140.2:n.909A>C
ENST00000640250.2:n.263A>C
ENST00000640681.2:n.868A>C
ENST00000696723.1:n.4397A>C
ENST00000696741.1:n.2402A>C
ENST00000696742.1:n.2129A>C
ENST00000696743.1:n.3532A>C
ENST00000696744.1:n.803A>C
ENST00000696767.1:n.1098A>C
ENST00000696768.1:c.*87A>C	ENSP00000512859.1:n.*87A>C
ENST00000696769.1:n.2453A>C
ENST00000696771.1:c.47A>C	ENSP00000512860.1:p.Asn16Thr
ENST00000696772.1:n.2367A>C
ENST00000696773.1:n.2106A>C
ENST00000696774.1:n.5874A>C
ENST00000696776.1:c.857A>C	ENSP00000512861.1:p.Asn286Thr
ENST00000696777.1:n.2172A>C
ENST00000696778.1:n.1200A>C
ENST00000696779.1:c.371A>C	ENSP00000512862.1:p.Asn124Thr
ENST00000696780.1:c.794A>C	ENSP00000512863.1:p.Asn265Thr
ENST00000696781.1:c.509A>C	ENSP00000512864.1:p.Asn170Thr
ENST00000696782.1:c.*166A>C	ENSP00000512865.1:n.*166A>C
ENST00000696783.1:n.2632A>C
ENST00000696992.1:n.1881A>C
ENST00000696995.1:n.4293A>C
ENST00000696996.1:n.2206A>C
ENST00000696997.1:c.*394A>C	ENSP00000513028.1:n.*394A>C
ENST00000696998.1:n.2018A>C
ENST00000696999.1:c.47A>C	ENSP00000513029.1:p.Asn16Thr
ENST00000697035.1:c.*97A>C	ENSP00000513059.1:n.*97A>C
ENST00000697036.1:c.*180A>C	ENSP00000513060.1:n.*180A>C
ENST00000697037.1:n.799A>C
ENST00000697093.1:n.3000A>C
ENST00000697094.1:n.3347A>C
ENST00000697095.1:c.*1965A>C	ENSP00000513104.1:n.*1965A>C
ENST00000697096.1:n.1897A>C
ENST00000697097.1:c.47A>C	ENSP00000513105.1:p.Asn16Thr
ENST00000562983.2:n.950A>C
ENST00000690268.1:c.845A>C	ENSP00000509810.1:p.Asn282Thr
ENST00000355740.7:c.*90A>C	ENSP00000347979.3:n.*90A>C
ENST00000612663.5:c.*166A>C	ENSP00000477997.3:n.*166A>C
ENST00000640140.1:n.936A>C
ENST00000640250.1:n.263A>C
ENST00000640681.1:n.885A>C
ENST00000652046.1:c.764A>C MANE Select	ENSP00000498466.1:p.Asn255Thr
ENST00000352159.8:c.*81A>C	ENSP00000345601.4:n.*81A>C
ENST00000355279.2:c.739A>C	ENSP00000347426.2:n.739A>C
ENST00000355740.6:c.764A>C	ENSP00000347979.2:p.Asn255Thr
ENST00000357339.6:c.701A>C	ENSP00000349896.2:p.Asn234Thr
ENST00000479522.5:c.*193A>C	ENSP00000424113.1:n.*193A>C
ENST00000484444.5:c.*205A>C	ENSP00000420975.1:n.*205A>C
ENST00000488877.5:c.*205A>C	ENSP00000425159.1:n.*205A>C
ENST00000492756.5:c.592A>C	ENSP00000422453.1:n.592A>C
ENST00000494410.5:c.*122A>C	ENSP00000423755.1:n.*122A>C
ENST00000494799.5:n.671A>C
ENST00000612663.4:c.*111A>C	ENSP00000477997.2:n.*111A>C
ENST00000615406.4:c.762A>C	ENSP00000484575.1:p.Gln254His
NM_000043.4:c.764A>C , LRG_134t1:c.764A>C	NP_000034.1:p.Asn255Thr
NM_152871.2:c.701A>C	NP_690610.1:p.Asn234Thr
NM_152872.2:c.*76A>C	NP_690611.1:n.*76A>C
NR_028033.2:n.938A>C
NR_028034.2:n.800A>C
NR_028035.2:n.863A>C
NR_028036.2:n.1001A>C
XM_006717819.2:c.845A>C	XP_006717882.1:p.Asn282Thr
XM_011539764.1:c.926A>C	XP_011538066.1:p.Asn309Thr
XM_011539765.1:c.863A>C	XP_011538067.1:p.Asn288Thr
XM_011539766.1:c.845A>C	XP_011538068.1:p.Asn282Thr
XM_011539767.1:c.809A>C	XP_011538069.1:p.Asn270Thr
XR_945732.1:n.832A>C
XR_945733.1:n.769A>C
NM_000043.5:c.764A>C	NP_000034.1:p.Asn255Thr
NM_001320619.1:c.*87A>C	NP_001307548.1:n.*87A>C
NM_152871.3:c.701A>C	NP_690610.1:p.Asn234Thr
NM_152872.3:c.*76A>C	NP_690611.1:n.*76A>C
NR_028033.3:n.910A>C
NR_028034.3:n.772A>C
NR_028035.3:n.835A>C
NR_028036.3:n.973A>C
NR_135313.1:n.890A>C
NR_135314.1:n.1073A>C
NR_135315.1:n.826A>C
XM_006717819.3:c.845A>C	XP_006717882.1:p.Asn282Thr
XM_011539764.2:c.926A>C	XP_011538066.1:p.Asn309Thr
XM_011539765.2:c.863A>C	XP_011538067.1:p.Asn288Thr
XM_011539766.2:c.845A>C	XP_011538068.1:p.Asn282Thr
XM_011539767.3:c.809A>C	XP_011538069.1:p.Asn270Thr
XR_945732.3:n.832A>C
XR_945733.2:n.769A>C
NM_000043.6:c.764A>C MANE Select	NP_000034.1:p.Asn255Thr
NM_001320619.2:c.*87A>C	NP_001307548.1:n.*87A>C
NM_152871.4:c.701A>C	NP_690610.1:p.Asn234Thr
NM_152872.4:c.*76A>C	NP_690611.1:n.*76A>C
NR_028033.4:n.671A>C
NR_028034.4:n.533A>C
NR_028035.4:n.596A>C
NR_028036.4:n.734A>C
NR_135313.2:n.651A>C
NR_135314.2:n.930A>C
NR_135315.2:n.683A>C