Canonical Allele Identifier: CA377510259

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774185A>C (hg19) ; chr10:g.89014428A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014428A>C , CM000672.2:g.89014428A>C	GRCh38
NC_000010.10:g.90774185A>C , CM000672.1:g.90774185A>C	GRCh37
NC_000010.9:g.90764165A>C	NCBI36
NG_009089.2:g.28898A>C , LRG_134:g.28898A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1295A>C
ENST00000355740.8:c.*309A>C	ENSP00000347979.3:n.*309A>C
ENST00000357339.7:c.923A>C	ENSP00000349896.2:p.Asn308Thr
ENST00000371857.8:n.2531A>C
ENST00000460510.6:c.269A>C	ENSP00000512812.1:p.Asn90Thr
ENST00000466081.6:n.2635A>C
ENST00000477270.6:c.1031A>C	ENSP00000512813.1:p.Asn344Thr
ENST00000479522.6:c.*415A>C	ENSP00000424113.1:n.*415A>C
ENST00000484444.6:c.*427A>C	ENSP00000420975.1:n.*427A>C
ENST00000488877.6:c.877A>C	ENSP00000425159.1:n.877A>C
ENST00000492756.7:c.*415A>C	ENSP00000422453.1:n.*415A>C
ENST00000494799.6:c.269A>C	ENSP00000512834.1:p.Asn90Thr
ENST00000562983.3:c.269A>C	ENSP00000512845.1:p.Asn90Thr
ENST00000612663.6:c.*388A>C	ENSP00000477997.3:n.*388A>C
ENST00000640140.2:n.1131A>C
ENST00000640250.2:n.485A>C
ENST00000640681.2:n.1090A>C
ENST00000696723.1:n.4619A>C
ENST00000696741.1:n.2624A>C
ENST00000696742.1:n.2351A>C
ENST00000696743.1:n.3754A>C
ENST00000696744.1:n.1025A>C
ENST00000696767.1:n.1320A>C
ENST00000696768.1:c.*309A>C	ENSP00000512859.1:n.*309A>C
ENST00000696769.1:n.2675A>C
ENST00000696771.1:c.269A>C	ENSP00000512860.1:p.Asn90Thr
ENST00000696772.1:n.2589A>C
ENST00000696773.1:n.2328A>C
ENST00000696774.1:n.6096A>C
ENST00000696776.1:c.1079A>C	ENSP00000512861.1:p.Asn360Thr
ENST00000696777.1:n.2394A>C
ENST00000696778.1:n.1422A>C
ENST00000696779.1:c.593A>C	ENSP00000512862.1:p.Asn198Thr
ENST00000696780.1:c.1016A>C	ENSP00000512863.1:p.Asn339Thr
ENST00000696781.1:c.731A>C	ENSP00000512864.1:p.Asn244Thr
ENST00000696782.1:c.*388A>C	ENSP00000512865.1:n.*388A>C
ENST00000696783.1:n.2854A>C
ENST00000696992.1:n.2103A>C
ENST00000696995.1:n.4515A>C
ENST00000696996.1:n.2428A>C
ENST00000696997.1:c.*616A>C	ENSP00000513028.1:n.*616A>C
ENST00000696998.1:n.2240A>C
ENST00000696999.1:c.269A>C	ENSP00000513029.1:p.Asn90Thr
ENST00000697036.1:c.*402A>C	ENSP00000513060.1:n.*402A>C
ENST00000697037.1:n.1021A>C
ENST00000697093.1:n.3222A>C
ENST00000697094.1:n.3569A>C
ENST00000697095.1:c.*2187A>C	ENSP00000513104.1:n.*2187A>C
ENST00000697096.1:n.2119A>C
ENST00000697097.1:c.269A>C	ENSP00000513105.1:p.Asn90Thr
ENST00000562983.2:n.1172A>C
ENST00000690268.1:c.1067A>C	ENSP00000509810.1:p.Asn356Thr
ENST00000355740.7:c.*312A>C	ENSP00000347979.3:n.*312A>C
ENST00000612663.5:c.*388A>C	ENSP00000477997.3:n.*388A>C
ENST00000640140.1:n.1158A>C
ENST00000640250.1:n.485A>C
ENST00000640681.1:n.1107A>C
ENST00000652046.1:c.986A>C MANE Select	ENSP00000498466.1:p.Asn329Thr
ENST00000352159.8:c.*303A>C	ENSP00000345601.4:n.*303A>C
ENST00000355279.2:c.961A>C	ENSP00000347426.2:n.961A>C
ENST00000355740.6:c.986A>C	ENSP00000347979.2:p.Asn329Thr
ENST00000357339.6:c.923A>C	ENSP00000349896.2:p.Asn308Thr
ENST00000479522.5:c.*415A>C	ENSP00000424113.1:n.*415A>C
ENST00000484444.5:c.*427A>C	ENSP00000420975.1:n.*427A>C
ENST00000488877.5:c.*427A>C	ENSP00000425159.1:n.*427A>C
ENST00000492756.5:c.814A>C	ENSP00000422453.1:n.814A>C
ENST00000494410.5:c.*344A>C	ENSP00000423755.1:n.*344A>C
ENST00000612663.4:c.*333A>C	ENSP00000477997.2:n.*333A>C
NM_000043.4:c.986A>C , LRG_134t1:c.986A>C	NP_000034.1:p.Asn329Thr
NM_152871.2:c.923A>C	NP_690610.1:p.Asn308Thr
NM_152872.2:c.*298A>C	NP_690611.1:n.*298A>C
NR_028033.2:n.1160A>C
NR_028034.2:n.1022A>C
NR_028035.2:n.1085A>C
NR_028036.2:n.1223A>C
XM_006717819.2:c.1067A>C	XP_006717882.1:p.Asn356Thr
XM_011539764.1:c.1148A>C	XP_011538066.1:p.Asn383Thr
XM_011539765.1:c.1085A>C	XP_011538067.1:p.Asn362Thr
XM_011539766.1:c.1067A>C	XP_011538068.1:p.Asn356Thr
XM_011539767.1:c.1031A>C	XP_011538069.1:p.Asn344Thr
XR_945733.1:n.991A>C
NM_000043.5:c.986A>C	NP_000034.1:p.Asn329Thr
NM_001320619.1:c.*309A>C	NP_001307548.1:n.*309A>C
NM_152871.3:c.923A>C	NP_690610.1:p.Asn308Thr
NM_152872.3:c.*298A>C	NP_690611.1:n.*298A>C
NR_028033.3:n.1132A>C
NR_028034.3:n.994A>C
NR_028035.3:n.1057A>C
NR_028036.3:n.1195A>C
NR_135313.1:n.1112A>C
NR_135314.1:n.1295A>C
NR_135315.1:n.1048A>C
XM_006717819.3:c.1067A>C	XP_006717882.1:p.Asn356Thr
XM_011539764.2:c.1148A>C	XP_011538066.1:p.Asn383Thr
XM_011539765.2:c.1085A>C	XP_011538067.1:p.Asn362Thr
XM_011539766.2:c.1067A>C	XP_011538068.1:p.Asn356Thr
XM_011539767.3:c.1031A>C	XP_011538069.1:p.Asn344Thr
XR_945732.3:n.1054A>C
XR_945733.2:n.991A>C
NM_000043.6:c.986A>C MANE Select	NP_000034.1:p.Asn329Thr
NM_001320619.2:c.*309A>C	NP_001307548.1:n.*309A>C
NM_152871.4:c.923A>C	NP_690610.1:p.Asn308Thr
NM_152872.4:c.*298A>C	NP_690611.1:n.*298A>C
NR_028033.4:n.893A>C
NR_028034.4:n.755A>C
NR_028035.4:n.818A>C
NR_028036.4:n.956A>C
NR_135313.2:n.873A>C
NR_135314.2:n.1152A>C
NR_135315.2:n.905A>C