Canonical Allele Identifier: CA377509622

Gene: FAS

Linked Data

• gnomAD v4: 10-89014155-G-C
• MyVariant Identifiers: chr10:g.90773912G>C (hg19) ; chr10:g.89014155G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014155G>C , CM000672.2:g.89014155G>C	GRCh38
NC_000010.10:g.90773912G>C , CM000672.1:g.90773912G>C	GRCh37
NC_000010.9:g.90763892G>C	NCBI36
NG_009089.2:g.28625G>C , LRG_134:g.28625G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1022G>C
ENST00000355740.8:c.*36G>C	ENSP00000347979.3:n.*36G>C
ENST00000357339.7:c.650G>C	ENSP00000349896.2:p.Gly217Ala
ENST00000371857.8:n.2258G>C
ENST00000460510.6:c.-5G>C	ENSP00000512812.1:n.-5G>C
ENST00000466081.6:n.2362G>C
ENST00000477270.6:c.758G>C	ENSP00000512813.1:p.Gly253Ala
ENST00000479522.6:c.*142G>C	ENSP00000424113.1:n.*142G>C
ENST00000484444.6:c.*154G>C	ENSP00000420975.1:n.*154G>C
ENST00000488877.6:c.604G>C	ENSP00000425159.1:n.604G>C
ENST00000492756.7:c.*142G>C	ENSP00000422453.1:n.*142G>C
ENST00000494799.6:c.-5G>C	ENSP00000512834.1:n.-5G>C
ENST00000562983.3:c.-5G>C	ENSP00000512845.1:n.-5G>C
ENST00000612663.6:c.*115G>C	ENSP00000477997.3:n.*115G>C
ENST00000640140.2:n.858G>C
ENST00000640250.2:n.212G>C
ENST00000640681.2:n.817G>C
ENST00000696723.1:n.4346G>C
ENST00000696741.1:n.2351G>C
ENST00000696742.1:n.2078G>C
ENST00000696743.1:n.3481G>C
ENST00000696744.1:n.752G>C
ENST00000696767.1:n.1047G>C
ENST00000696768.1:c.*36G>C	ENSP00000512859.1:n.*36G>C
ENST00000696769.1:n.2402G>C
ENST00000696771.1:c.-5G>C	ENSP00000512860.1:n.-5G>C
ENST00000696772.1:n.2316G>C
ENST00000696773.1:n.2055G>C
ENST00000696774.1:n.5823G>C
ENST00000696776.1:c.806G>C	ENSP00000512861.1:p.Gly269Ala
ENST00000696777.1:n.2121G>C
ENST00000696778.1:n.1149G>C
ENST00000696779.1:c.320G>C	ENSP00000512862.1:p.Gly107Ala
ENST00000696780.1:c.743G>C	ENSP00000512863.1:p.Gly248Ala
ENST00000696781.1:c.458G>C	ENSP00000512864.1:p.Gly153Ala
ENST00000696782.1:c.*115G>C	ENSP00000512865.1:n.*115G>C
ENST00000696783.1:n.2581G>C
ENST00000696992.1:n.1830G>C
ENST00000696995.1:n.4242G>C
ENST00000696996.1:n.2155G>C
ENST00000696997.1:c.*343G>C	ENSP00000513028.1:n.*343G>C
ENST00000696998.1:n.1967G>C
ENST00000696999.1:c.-5G>C	ENSP00000513029.1:n.-5G>C
ENST00000697035.1:c.*46G>C	ENSP00000513059.1:n.*46G>C
ENST00000697036.1:c.*129G>C	ENSP00000513060.1:n.*129G>C
ENST00000697037.1:n.748G>C
ENST00000697093.1:n.2949G>C
ENST00000697094.1:n.3296G>C
ENST00000697095.1:c.*1914G>C	ENSP00000513104.1:n.*1914G>C
ENST00000697096.1:n.1846G>C
ENST00000697097.1:c.-5G>C	ENSP00000513105.1:n.-5G>C
ENST00000562983.2:n.899G>C
ENST00000690268.1:c.794G>C	ENSP00000509810.1:p.Gly265Ala
ENST00000355740.7:c.*39G>C	ENSP00000347979.3:n.*39G>C
ENST00000612663.5:c.*115G>C	ENSP00000477997.3:n.*115G>C
ENST00000640140.1:n.885G>C
ENST00000640250.1:n.212G>C
ENST00000640681.1:n.834G>C
ENST00000652046.1:c.713G>C MANE Select	ENSP00000498466.1:p.Gly238Ala
ENST00000313771.9:n.1022G>C
ENST00000352159.8:c.*30G>C	ENSP00000345601.4:n.*30G>C
ENST00000355279.2:c.688G>C	ENSP00000347426.2:n.688G>C
ENST00000355740.6:c.713G>C	ENSP00000347979.2:p.Gly238Ala
ENST00000357339.6:c.650G>C	ENSP00000349896.2:p.Gly217Ala
ENST00000479522.5:c.*142G>C	ENSP00000424113.1:n.*142G>C
ENST00000484444.5:c.*154G>C	ENSP00000420975.1:n.*154G>C
ENST00000488877.5:c.*154G>C	ENSP00000425159.1:n.*154G>C
ENST00000492756.5:c.541G>C	ENSP00000422453.1:n.541G>C
ENST00000494410.5:c.*71G>C	ENSP00000423755.1:n.*71G>C
ENST00000494799.5:n.620G>C
ENST00000612663.4:c.*60G>C	ENSP00000477997.2:n.*60G>C
ENST00000615406.4:c.713G>C	ENSP00000484575.1:p.Gly238Ala
ENST00000626542.2:c.711G>C	ENSP00000485876.1:p.Trp237Cys
NM_000043.4:c.713G>C , LRG_134t1:c.713G>C	NP_000034.1:p.Gly238Ala
NM_152871.2:c.650G>C	NP_690610.1:p.Gly217Ala
NM_152872.2:c.*25G>C	NP_690611.1:n.*25G>C
NR_028033.2:n.887G>C
NR_028034.2:n.749G>C
NR_028035.2:n.812G>C
NR_028036.2:n.950G>C
XM_006717819.2:c.794G>C	XP_006717882.1:p.Gly265Ala
XM_011539764.1:c.875G>C	XP_011538066.1:p.Gly292Ala
XM_011539765.1:c.812G>C	XP_011538067.1:p.Gly271Ala
XM_011539766.1:c.794G>C	XP_011538068.1:p.Gly265Ala
XM_011539767.1:c.758G>C	XP_011538069.1:p.Gly253Ala
XR_945732.1:n.781G>C
XR_945733.1:n.718G>C
NM_000043.5:c.713G>C	NP_000034.1:p.Gly238Ala
NM_001320619.1:c.*36G>C	NP_001307548.1:n.*36G>C
NM_152871.3:c.650G>C	NP_690610.1:p.Gly217Ala
NM_152872.3:c.*25G>C	NP_690611.1:n.*25G>C
NR_028033.3:n.859G>C
NR_028034.3:n.721G>C
NR_028035.3:n.784G>C
NR_028036.3:n.922G>C
NR_135313.1:n.839G>C
NR_135314.1:n.1022G>C
NR_135315.1:n.775G>C
XM_006717819.3:c.794G>C	XP_006717882.1:p.Gly265Ala
XM_011539764.2:c.875G>C	XP_011538066.1:p.Gly292Ala
XM_011539765.2:c.812G>C	XP_011538067.1:p.Gly271Ala
XM_011539766.2:c.794G>C	XP_011538068.1:p.Gly265Ala
XM_011539767.3:c.758G>C	XP_011538069.1:p.Gly253Ala
XR_945732.3:n.781G>C
XR_945733.2:n.718G>C
NM_000043.6:c.713G>C MANE Select	NP_000034.1:p.Gly238Ala
NM_001320619.2:c.*36G>C	NP_001307548.1:n.*36G>C
NM_152871.4:c.650G>C	NP_690610.1:p.Gly217Ala
NM_152872.4:c.*25G>C	NP_690611.1:n.*25G>C
NR_028033.4:n.620G>C
NR_028034.4:n.482G>C
NR_028035.4:n.545G>C
NR_028036.4:n.683G>C
NR_135313.2:n.600G>C
NR_135314.2:n.879G>C
NR_135315.2:n.632G>C