Canonical Allele Identifier: CA377509574

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773896A>C (hg19) ; chr10:g.89014139A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014139A>C , CM000672.2:g.89014139A>C	GRCh38
NC_000010.10:g.90773896A>C , CM000672.1:g.90773896A>C	GRCh37
NC_000010.9:g.90763876A>C	NCBI36
NG_009089.2:g.28609A>C , LRG_134:g.28609A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1006A>C
ENST00000355740.8:c.*20A>C	ENSP00000347979.3:n.*20A>C
ENST00000357339.7:c.634A>C	ENSP00000349896.2:p.Ile212Leu
ENST00000371857.8:n.2242A>C
ENST00000460510.6:c.-21A>C	ENSP00000512812.1:n.-21A>C
ENST00000466081.6:n.2346A>C
ENST00000477270.6:c.742A>C	ENSP00000512813.1:p.Ile248Leu
ENST00000479522.6:c.*126A>C	ENSP00000424113.1:n.*126A>C
ENST00000484444.6:c.*138A>C	ENSP00000420975.1:n.*138A>C
ENST00000488877.6:c.588A>C	ENSP00000425159.1:n.588A>C
ENST00000492756.7:c.*126A>C	ENSP00000422453.1:n.*126A>C
ENST00000494799.6:c.-21A>C	ENSP00000512834.1:n.-21A>C
ENST00000562983.3:c.-21A>C	ENSP00000512845.1:n.-21A>C
ENST00000612663.6:c.*99A>C	ENSP00000477997.3:n.*99A>C
ENST00000640140.2:n.842A>C
ENST00000640250.2:n.196A>C
ENST00000640681.2:n.801A>C
ENST00000696723.1:n.4330A>C
ENST00000696741.1:n.2335A>C
ENST00000696742.1:n.2062A>C
ENST00000696743.1:n.3465A>C
ENST00000696744.1:n.736A>C
ENST00000696767.1:n.1031A>C
ENST00000696768.1:c.*20A>C	ENSP00000512859.1:n.*20A>C
ENST00000696769.1:n.2386A>C
ENST00000696771.1:c.-21A>C	ENSP00000512860.1:n.-21A>C
ENST00000696772.1:n.2300A>C
ENST00000696773.1:n.2039A>C
ENST00000696774.1:n.5807A>C
ENST00000696776.1:c.790A>C	ENSP00000512861.1:p.Ile264Leu
ENST00000696777.1:n.2105A>C
ENST00000696778.1:n.1133A>C
ENST00000696779.1:c.304A>C	ENSP00000512862.1:p.Ile102Leu
ENST00000696780.1:c.727A>C	ENSP00000512863.1:p.Ile243Leu
ENST00000696781.1:c.442A>C	ENSP00000512864.1:p.Ile148Leu
ENST00000696782.1:c.*99A>C	ENSP00000512865.1:n.*99A>C
ENST00000696783.1:n.2565A>C
ENST00000696992.1:n.1814A>C
ENST00000696995.1:n.4226A>C
ENST00000696996.1:n.2139A>C
ENST00000696997.1:c.*327A>C	ENSP00000513028.1:n.*327A>C
ENST00000696998.1:n.1951A>C
ENST00000696999.1:c.-21A>C	ENSP00000513029.1:n.-21A>C
ENST00000697035.1:c.*30A>C	ENSP00000513059.1:n.*30A>C
ENST00000697036.1:c.*113A>C	ENSP00000513060.1:n.*113A>C
ENST00000697037.1:n.732A>C
ENST00000697093.1:n.2933A>C
ENST00000697094.1:n.3280A>C
ENST00000697095.1:c.*1898A>C	ENSP00000513104.1:n.*1898A>C
ENST00000697096.1:n.1830A>C
ENST00000697097.1:c.-21A>C	ENSP00000513105.1:n.-21A>C
ENST00000562983.2:n.883A>C
ENST00000690268.1:c.778A>C	ENSP00000509810.1:p.Ile260Leu
ENST00000355740.7:c.*23A>C	ENSP00000347979.3:n.*23A>C
ENST00000612663.5:c.*99A>C	ENSP00000477997.3:n.*99A>C
ENST00000640140.1:n.869A>C
ENST00000640250.1:n.196A>C
ENST00000640681.1:n.818A>C
ENST00000652046.1:c.697A>C MANE Select	ENSP00000498466.1:p.Ile233Leu
ENST00000313771.9:n.1006A>C
ENST00000352159.8:c.*14A>C	ENSP00000345601.4:n.*14A>C
ENST00000355279.2:c.672A>C	ENSP00000347426.2:n.672A>C
ENST00000355740.6:c.697A>C	ENSP00000347979.2:p.Ile233Leu
ENST00000357339.6:c.634A>C	ENSP00000349896.2:p.Ile212Leu
ENST00000479522.5:c.*126A>C	ENSP00000424113.1:n.*126A>C
ENST00000484444.5:c.*138A>C	ENSP00000420975.1:n.*138A>C
ENST00000488877.5:c.*138A>C	ENSP00000425159.1:n.*138A>C
ENST00000492756.5:c.525A>C	ENSP00000422453.1:n.525A>C
ENST00000494410.5:c.*55A>C	ENSP00000423755.1:n.*55A>C
ENST00000494799.5:n.604A>C
ENST00000612663.4:c.*44A>C	ENSP00000477997.2:n.*44A>C
ENST00000615406.4:c.697A>C	ENSP00000484575.1:p.Ile233Leu
ENST00000626542.2:c.697-2A>C	ENSP00000485876.1:n.697-2A>C
NM_000043.4:c.697A>C , LRG_134t1:c.697A>C	NP_000034.1:p.Ile233Leu
NM_152871.2:c.634A>C	NP_690610.1:p.Ile212Leu
NM_152872.2:c.*9A>C	NP_690611.1:n.*9A>C
NR_028033.2:n.871A>C
NR_028034.2:n.733A>C
NR_028035.2:n.796A>C
NR_028036.2:n.934A>C
XM_006717819.2:c.778A>C	XP_006717882.1:p.Ile260Leu
XM_011539764.1:c.859A>C	XP_011538066.1:p.Ile287Leu
XM_011539765.1:c.796A>C	XP_011538067.1:p.Ile266Leu
XM_011539766.1:c.778A>C	XP_011538068.1:p.Ile260Leu
XM_011539767.1:c.742A>C	XP_011538069.1:p.Ile248Leu
XR_945732.1:n.765A>C
XR_945733.1:n.702A>C
NM_000043.5:c.697A>C	NP_000034.1:p.Ile233Leu
NM_001320619.1:c.*20A>C	NP_001307548.1:n.*20A>C
NM_152871.3:c.634A>C	NP_690610.1:p.Ile212Leu
NM_152872.3:c.*9A>C	NP_690611.1:n.*9A>C
NR_028033.3:n.843A>C
NR_028034.3:n.705A>C
NR_028035.3:n.768A>C
NR_028036.3:n.906A>C
NR_135313.1:n.823A>C
NR_135314.1:n.1006A>C
NR_135315.1:n.759A>C
XM_006717819.3:c.778A>C	XP_006717882.1:p.Ile260Leu
XM_011539764.2:c.859A>C	XP_011538066.1:p.Ile287Leu
XM_011539765.2:c.796A>C	XP_011538067.1:p.Ile266Leu
XM_011539766.2:c.778A>C	XP_011538068.1:p.Ile260Leu
XM_011539767.3:c.742A>C	XP_011538069.1:p.Ile248Leu
XR_945732.3:n.765A>C
XR_945733.2:n.702A>C
NM_000043.6:c.697A>C MANE Select	NP_000034.1:p.Ile233Leu
NM_001320619.2:c.*20A>C	NP_001307548.1:n.*20A>C
NM_152871.4:c.634A>C	NP_690610.1:p.Ile212Leu
NM_152872.4:c.*9A>C	NP_690611.1:n.*9A>C
NR_028033.4:n.604A>C
NR_028034.4:n.466A>C
NR_028035.4:n.529A>C
NR_028036.4:n.667A>C
NR_135313.2:n.584A>C
NR_135314.2:n.863A>C
NR_135315.2:n.616A>C