Canonical Allele Identifier: CA2574605500

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014505T>C , CM000672.2:g.89014505T>C	GRCh38
NC_000010.10:g.90774262T>C , CM000672.1:g.90774262T>C	GRCh37
NC_000010.9:g.90764242T>C	NCBI36
NG_009089.2:g.28975T>C , LRG_134:g.28975T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1372T>C
ENST00000355740.8:c.*386T>C	ENSP00000347979.3:n.*386T>C
ENST00000357339.7:c.*55T>C	ENSP00000349896.2:n.*55T>C
ENST00000371857.8:n.2608T>C
ENST00000460510.6:c.*55T>C	ENSP00000512812.1:n.*55T>C
ENST00000466081.6:n.2712T>C
ENST00000477270.6:c.*55T>C	ENSP00000512813.1:n.*55T>C
ENST00000479522.6:c.*492T>C	ENSP00000424113.1:n.*492T>C
ENST00000484444.6:c.*504T>C	ENSP00000420975.1:n.*504T>C
ENST00000488877.6:c.954T>C	ENSP00000425159.1:n.954T>C
ENST00000492756.7:c.*492T>C	ENSP00000422453.1:n.*492T>C
ENST00000494799.6:c.*55T>C	ENSP00000512834.1:n.*55T>C
ENST00000562983.3:c.*55T>C	ENSP00000512845.1:n.*55T>C
ENST00000612663.6:c.*465T>C	ENSP00000477997.3:n.*465T>C
ENST00000640140.2:n.1208T>C
ENST00000640250.2:n.562T>C
ENST00000640681.2:n.1167T>C
ENST00000696723.1:n.4696T>C
ENST00000696741.1:n.2701T>C
ENST00000696742.1:n.2428T>C
ENST00000696743.1:n.3831T>C
ENST00000696744.1:n.1102T>C
ENST00000696767.1:n.1397T>C
ENST00000696768.1:c.*386T>C	ENSP00000512859.1:n.*386T>C
ENST00000696769.1:n.2752T>C
ENST00000696771.1:c.*55T>C	ENSP00000512860.1:n.*55T>C
ENST00000696772.1:n.2666T>C
ENST00000696773.1:n.2405T>C
ENST00000696774.1:n.6173T>C
ENST00000696776.1:c.*55T>C	ENSP00000512861.1:n.*55T>C
ENST00000696777.1:n.2471T>C
ENST00000696778.1:n.1499T>C
ENST00000696779.1:c.*55T>C	ENSP00000512862.1:n.*55T>C
ENST00000696780.1:c.*55T>C	ENSP00000512863.1:n.*55T>C
ENST00000696781.1:c.*55T>C	ENSP00000512864.1:n.*55T>C
ENST00000696782.1:c.*465T>C	ENSP00000512865.1:n.*465T>C
ENST00000696783.1:n.2931T>C
ENST00000696992.1:n.2180T>C
ENST00000696995.1:n.4592T>C
ENST00000696996.1:n.2505T>C
ENST00000696997.1:c.*693T>C	ENSP00000513028.1:n.*693T>C
ENST00000696998.1:n.2317T>C
ENST00000696999.1:c.*55T>C	ENSP00000513029.1:n.*55T>C
ENST00000697036.1:c.*479T>C	ENSP00000513060.1:n.*479T>C
ENST00000697037.1:n.1098T>C
ENST00000697093.1:n.3299T>C
ENST00000697094.1:n.3646T>C
ENST00000697095.1:c.*2264T>C	ENSP00000513104.1:n.*2264T>C
ENST00000697096.1:n.2196T>C
ENST00000697097.1:c.*55T>C	ENSP00000513105.1:n.*55T>C
ENST00000562983.2:n.1249T>C
ENST00000690268.1:c.*55T>C	ENSP00000509810.1:n.*55T>C
ENST00000355740.7:c.*389T>C	ENSP00000347979.3:n.*389T>C
ENST00000640140.1:n.1235T>C
ENST00000640250.1:n.562T>C
ENST00000640681.1:n.1184T>C
ENST00000652046.1:c.*55T>C MANE Select	ENSP00000498466.1:n.*55T>C
ENST00000352159.8:c.*380T>C	ENSP00000345601.4:n.*380T>C
ENST00000355740.6:c.*55T>C	ENSP00000347979.2:n.*55T>C
ENST00000479522.5:c.*492T>C	ENSP00000424113.1:n.*492T>C
ENST00000484444.5:c.*504T>C	ENSP00000420975.1:n.*504T>C
ENST00000494410.5:c.*421T>C	ENSP00000423755.1:n.*421T>C
NM_000043.4:c.*55T>C , LRG_134t1:c.*55T>C	NP_000034.1:n.*55T>C
NM_152871.2:c.*55T>C	NP_690610.1:n.*55T>C
NM_152872.2:c.*375T>C	NP_690611.1:n.*375T>C
NR_028033.2:n.1237T>C
NR_028034.2:n.1099T>C
NR_028035.2:n.1162T>C
NR_028036.2:n.1300T>C
XM_006717819.2:c.*55T>C	XP_006717882.1:n.*55T>C
XM_011539764.1:c.*55T>C	XP_011538066.1:n.*55T>C
XM_011539765.1:c.*55T>C	XP_011538067.1:n.*55T>C
XM_011539766.1:c.*55T>C	XP_011538068.1:n.*55T>C
XM_011539767.1:c.*55T>C	XP_011538069.1:n.*55T>C
XR_945733.1:n.1068T>C
NM_000043.5:c.*55T>C	NP_000034.1:n.*55T>C
NM_001320619.1:c.*386T>C	NP_001307548.1:n.*386T>C
NM_152871.3:c.*55T>C	NP_690610.1:n.*55T>C
NM_152872.3:c.*375T>C	NP_690611.1:n.*375T>C
NR_028033.3:n.1209T>C
NR_028034.3:n.1071T>C
NR_028035.3:n.1134T>C
NR_028036.3:n.1272T>C
NR_135313.1:n.1189T>C
NR_135314.1:n.1372T>C
NR_135315.1:n.1125T>C
XM_006717819.3:c.*55T>C	XP_006717882.1:n.*55T>C
XM_011539764.2:c.*55T>C	XP_011538066.1:n.*55T>C
XM_011539765.2:c.*55T>C	XP_011538067.1:n.*55T>C
XM_011539766.2:c.*55T>C	XP_011538068.1:n.*55T>C
XM_011539767.3:c.*55T>C	XP_011538069.1:n.*55T>C
XR_945732.3:n.1131T>C
XR_945733.2:n.1068T>C
NM_000043.6:c.*55T>C MANE Select	NP_000034.1:n.*55T>C
NM_001320619.2:c.*386T>C	NP_001307548.1:n.*386T>C
NM_152871.4:c.*55T>C	NP_690610.1:n.*55T>C
NM_152872.4:c.*375T>C	NP_690611.1:n.*375T>C
NR_028033.4:n.970T>C
NR_028034.4:n.832T>C
NR_028035.4:n.895T>C
NR_028036.4:n.1033T>C
NR_135313.2:n.950T>C
NR_135314.2:n.1229T>C
NR_135315.2:n.982T>C