Canonical Allele Identifier: CA377509560

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773890A>C (hg19) ; chr10:g.89014133A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014133A>C , CM000672.2:g.89014133A>C	GRCh38
NC_000010.10:g.90773890A>C , CM000672.1:g.90773890A>C	GRCh37
NC_000010.9:g.90763870A>C	NCBI36
NG_009089.2:g.28603A>C , LRG_134:g.28603A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.1000A>C
ENST00000355740.8:c.*14A>C	ENSP00000347979.3:n.*14A>C
ENST00000357339.7:c.628A>C	ENSP00000349896.2:p.Lys210Gln
ENST00000371857.8:n.2236A>C
ENST00000460510.6:c.-27A>C	ENSP00000512812.1:n.-27A>C
ENST00000466081.6:n.2340A>C
ENST00000477270.6:c.736A>C	ENSP00000512813.1:p.Lys246Gln
ENST00000479522.6:c.*120A>C	ENSP00000424113.1:n.*120A>C
ENST00000484444.6:c.*132A>C	ENSP00000420975.1:n.*132A>C
ENST00000488877.6:c.582A>C	ENSP00000425159.1:n.582A>C
ENST00000492756.7:c.*120A>C	ENSP00000422453.1:n.*120A>C
ENST00000494799.6:c.-27A>C	ENSP00000512834.1:n.-27A>C
ENST00000562983.3:c.-27A>C	ENSP00000512845.1:n.-27A>C
ENST00000612663.6:c.*93A>C	ENSP00000477997.3:n.*93A>C
ENST00000640140.2:n.836A>C
ENST00000640250.2:n.190A>C
ENST00000640681.2:n.795A>C
ENST00000696723.1:n.4324A>C
ENST00000696741.1:n.2329A>C
ENST00000696742.1:n.2056A>C
ENST00000696743.1:n.3459A>C
ENST00000696744.1:n.730A>C
ENST00000696767.1:n.1025A>C
ENST00000696768.1:c.*14A>C	ENSP00000512859.1:n.*14A>C
ENST00000696769.1:n.2380A>C
ENST00000696771.1:c.-27A>C	ENSP00000512860.1:n.-27A>C
ENST00000696772.1:n.2294A>C
ENST00000696773.1:n.2033A>C
ENST00000696774.1:n.5801A>C
ENST00000696776.1:c.784A>C	ENSP00000512861.1:p.Lys262Gln
ENST00000696777.1:n.2099A>C
ENST00000696778.1:n.1127A>C
ENST00000696779.1:c.298A>C	ENSP00000512862.1:p.Lys100Gln
ENST00000696780.1:c.721A>C	ENSP00000512863.1:p.Lys241Gln
ENST00000696781.1:c.436A>C	ENSP00000512864.1:p.Lys146Gln
ENST00000696782.1:c.*93A>C	ENSP00000512865.1:n.*93A>C
ENST00000696783.1:n.2559A>C
ENST00000696992.1:n.1808A>C
ENST00000696995.1:n.4220A>C
ENST00000696996.1:n.2133A>C
ENST00000696997.1:c.*321A>C	ENSP00000513028.1:n.*321A>C
ENST00000696998.1:n.1945A>C
ENST00000696999.1:c.-27A>C	ENSP00000513029.1:n.-27A>C
ENST00000697035.1:c.*24A>C	ENSP00000513059.1:n.*24A>C
ENST00000697036.1:c.*107A>C	ENSP00000513060.1:n.*107A>C
ENST00000697037.1:n.726A>C
ENST00000697093.1:n.2927A>C
ENST00000697094.1:n.3274A>C
ENST00000697095.1:c.*1892A>C	ENSP00000513104.1:n.*1892A>C
ENST00000697096.1:n.1824A>C
ENST00000697097.1:c.-27A>C	ENSP00000513105.1:n.-27A>C
ENST00000562983.2:n.877A>C
ENST00000690268.1:c.772A>C	ENSP00000509810.1:p.Lys258Gln
ENST00000355740.7:c.*17A>C	ENSP00000347979.3:n.*17A>C
ENST00000612663.5:c.*93A>C	ENSP00000477997.3:n.*93A>C
ENST00000640140.1:n.863A>C
ENST00000640250.1:n.190A>C
ENST00000640681.1:n.812A>C
ENST00000652046.1:c.691A>C MANE Select	ENSP00000498466.1:p.Lys231Gln
ENST00000313771.9:n.1000A>C
ENST00000352159.8:c.*8A>C	ENSP00000345601.4:n.*8A>C
ENST00000355279.2:c.666A>C	ENSP00000347426.2:n.666A>C
ENST00000355740.6:c.691A>C	ENSP00000347979.2:p.Lys231Gln
ENST00000357339.6:c.628A>C	ENSP00000349896.2:p.Lys210Gln
ENST00000479522.5:c.*120A>C	ENSP00000424113.1:n.*120A>C
ENST00000484444.5:c.*132A>C	ENSP00000420975.1:n.*132A>C
ENST00000488877.5:c.*132A>C	ENSP00000425159.1:n.*132A>C
ENST00000492756.5:c.519A>C	ENSP00000422453.1:n.519A>C
ENST00000494410.5:c.*49A>C	ENSP00000423755.1:n.*49A>C
ENST00000494799.5:n.598A>C
ENST00000612663.4:c.*38A>C	ENSP00000477997.2:n.*38A>C
ENST00000615406.4:c.691A>C	ENSP00000484575.1:p.Lys231Gln
ENST00000626542.2:c.691A>C	ENSP00000485876.1:p.Lys231Gln
NM_000043.4:c.691A>C , LRG_134t1:c.691A>C	NP_000034.1:p.Lys231Gln
NM_152871.2:c.628A>C	NP_690610.1:p.Lys210Gln
NM_152872.2:c.*3A>C	NP_690611.1:n.*3A>C
NR_028033.2:n.865A>C
NR_028034.2:n.727A>C
NR_028035.2:n.790A>C
NR_028036.2:n.928A>C
XM_006717819.2:c.772A>C	XP_006717882.1:p.Lys258Gln
XM_011539764.1:c.853A>C	XP_011538066.1:p.Lys285Gln
XM_011539765.1:c.790A>C	XP_011538067.1:p.Lys264Gln
XM_011539766.1:c.772A>C	XP_011538068.1:p.Lys258Gln
XM_011539767.1:c.736A>C	XP_011538069.1:p.Lys246Gln
XR_945732.1:n.759A>C
XR_945733.1:n.696A>C
NM_000043.5:c.691A>C	NP_000034.1:p.Lys231Gln
NM_001320619.1:c.*14A>C	NP_001307548.1:n.*14A>C
NM_152871.3:c.628A>C	NP_690610.1:p.Lys210Gln
NM_152872.3:c.*3A>C	NP_690611.1:n.*3A>C
NR_028033.3:n.837A>C
NR_028034.3:n.699A>C
NR_028035.3:n.762A>C
NR_028036.3:n.900A>C
NR_135313.1:n.817A>C
NR_135314.1:n.1000A>C
NR_135315.1:n.753A>C
XM_006717819.3:c.772A>C	XP_006717882.1:p.Lys258Gln
XM_011539764.2:c.853A>C	XP_011538066.1:p.Lys285Gln
XM_011539765.2:c.790A>C	XP_011538067.1:p.Lys264Gln
XM_011539766.2:c.772A>C	XP_011538068.1:p.Lys258Gln
XM_011539767.3:c.736A>C	XP_011538069.1:p.Lys246Gln
XR_945732.3:n.759A>C
XR_945733.2:n.696A>C
NM_000043.6:c.691A>C MANE Select	NP_000034.1:p.Lys231Gln
NM_001320619.2:c.*14A>C	NP_001307548.1:n.*14A>C
NM_152871.4:c.628A>C	NP_690610.1:p.Lys210Gln
NM_152872.4:c.*3A>C	NP_690611.1:n.*3A>C
NR_028033.4:n.598A>C
NR_028034.4:n.460A>C
NR_028035.4:n.523A>C
NR_028036.4:n.661A>C
NR_135313.2:n.578A>C
NR_135314.2:n.857A>C
NR_135315.2:n.610A>C