Canonical Allele Identifier: CA211335487

Gene: FAS

Linked Data

• dbSNP Id: rs79516148
• MyVariant Identifiers: chr10:g.90774281A>C (hg19) ; chr10:g.89014524A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014524A>C , CM000672.2:g.89014524A>C	GRCh38
NC_000010.10:g.90774281A>C , CM000672.1:g.90774281A>C	GRCh37
NC_000010.9:g.90764261A>C	NCBI36
NG_009089.2:g.28994A>C , LRG_134:g.28994A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1391A>C
ENST00000355740.8:c.*405A>C	ENSP00000347979.3:n.*405A>C
ENST00000357339.7:c.*74A>C	ENSP00000349896.2:n.*74A>C
ENST00000371857.8:n.2627A>C
ENST00000460510.6:c.*74A>C	ENSP00000512812.1:n.*74A>C
ENST00000466081.6:n.2731A>C
ENST00000477270.6:c.*74A>C	ENSP00000512813.1:n.*74A>C
ENST00000479522.6:c.*511A>C	ENSP00000424113.1:n.*511A>C
ENST00000484444.6:c.*523A>C	ENSP00000420975.1:n.*523A>C
ENST00000488877.6:c.973A>C	ENSP00000425159.1:n.973A>C
ENST00000492756.7:c.*511A>C	ENSP00000422453.1:n.*511A>C
ENST00000494799.6:c.*74A>C	ENSP00000512834.1:n.*74A>C
ENST00000562983.3:c.*74A>C	ENSP00000512845.1:n.*74A>C
ENST00000612663.6:c.*484A>C	ENSP00000477997.3:n.*484A>C
ENST00000640140.2:n.1227A>C
ENST00000640250.2:n.581A>C
ENST00000640681.2:n.1186A>C
ENST00000696723.1:n.4715A>C
ENST00000696741.1:n.2720A>C
ENST00000696742.1:n.2447A>C
ENST00000696743.1:n.3850A>C
ENST00000696744.1:n.1121A>C
ENST00000696767.1:n.1416A>C
ENST00000696768.1:c.*405A>C	ENSP00000512859.1:n.*405A>C
ENST00000696769.1:n.2771A>C
ENST00000696771.1:c.*74A>C	ENSP00000512860.1:n.*74A>C
ENST00000696772.1:n.2685A>C
ENST00000696773.1:n.2424A>C
ENST00000696774.1:n.6192A>C
ENST00000696776.1:c.*74A>C	ENSP00000512861.1:n.*74A>C
ENST00000696777.1:n.2490A>C
ENST00000696778.1:n.1518A>C
ENST00000696779.1:c.*74A>C	ENSP00000512862.1:n.*74A>C
ENST00000696780.1:c.*74A>C	ENSP00000512863.1:n.*74A>C
ENST00000696781.1:c.*74A>C	ENSP00000512864.1:n.*74A>C
ENST00000696782.1:c.*484A>C	ENSP00000512865.1:n.*484A>C
ENST00000696783.1:n.2950A>C
ENST00000696992.1:n.2199A>C
ENST00000696995.1:n.4611A>C
ENST00000696996.1:n.2524A>C
ENST00000696997.1:c.*712A>C	ENSP00000513028.1:n.*712A>C
ENST00000696998.1:n.2336A>C
ENST00000696999.1:c.*74A>C	ENSP00000513029.1:n.*74A>C
ENST00000697036.1:c.*498A>C	ENSP00000513060.1:n.*498A>C
ENST00000697037.1:n.1117A>C
ENST00000697093.1:n.3318A>C
ENST00000697094.1:n.3665A>C
ENST00000697095.1:c.*2283A>C	ENSP00000513104.1:n.*2283A>C
ENST00000697096.1:n.2215A>C
ENST00000697097.1:c.*74A>C	ENSP00000513105.1:n.*74A>C
ENST00000562983.2:n.1268A>C
ENST00000690268.1:c.*74A>C	ENSP00000509810.1:n.*74A>C
ENST00000355740.7:c.*408A>C	ENSP00000347979.3:n.*408A>C
ENST00000640140.1:n.1254A>C
ENST00000640250.1:n.581A>C
ENST00000640681.1:n.1203A>C
ENST00000652046.1:c.*74A>C MANE Select	ENSP00000498466.1:n.*74A>C
ENST00000352159.8:c.*399A>C	ENSP00000345601.4:n.*399A>C
ENST00000355740.6:c.*74A>C	ENSP00000347979.2:n.*74A>C
ENST00000479522.5:c.*511A>C	ENSP00000424113.1:n.*511A>C
ENST00000484444.5:c.*523A>C	ENSP00000420975.1:n.*523A>C
ENST00000494410.5:c.*440A>C	ENSP00000423755.1:n.*440A>C
NM_000043.4:c.*74A>C , LRG_134t1:c.*74A>C	NP_000034.1:n.*74A>C
NM_152871.2:c.*74A>C	NP_690610.1:n.*74A>C
NM_152872.2:c.*394A>C	NP_690611.1:n.*394A>C
NR_028033.2:n.1256A>C
NR_028034.2:n.1118A>C
NR_028035.2:n.1181A>C
NR_028036.2:n.1319A>C
XM_006717819.2:c.*74A>C	XP_006717882.1:n.*74A>C
XM_011539764.1:c.*74A>C	XP_011538066.1:n.*74A>C
XM_011539765.1:c.*74A>C	XP_011538067.1:n.*74A>C
XM_011539766.1:c.*74A>C	XP_011538068.1:n.*74A>C
XM_011539767.1:c.*74A>C	XP_011538069.1:n.*74A>C
NM_000043.5:c.*74A>C	NP_000034.1:n.*74A>C
NM_001320619.1:c.*405A>C	NP_001307548.1:n.*405A>C
NM_152871.3:c.*74A>C	NP_690610.1:n.*74A>C
NM_152872.3:c.*394A>C	NP_690611.1:n.*394A>C
NR_028033.3:n.1228A>C
NR_028034.3:n.1090A>C
NR_028035.3:n.1153A>C
NR_028036.3:n.1291A>C
NR_135313.1:n.1208A>C
NR_135314.1:n.1391A>C
NR_135315.1:n.1144A>C
XM_006717819.3:c.*74A>C	XP_006717882.1:n.*74A>C
XM_011539764.2:c.*74A>C	XP_011538066.1:n.*74A>C
XM_011539765.2:c.*74A>C	XP_011538067.1:n.*74A>C
XM_011539766.2:c.*74A>C	XP_011538068.1:n.*74A>C
XM_011539767.3:c.*74A>C	XP_011538069.1:n.*74A>C
XR_945732.3:n.1150A>C
XR_945733.2:n.1087A>C
NM_000043.6:c.*74A>C MANE Select	NP_000034.1:n.*74A>C
NM_001320619.2:c.*405A>C	NP_001307548.1:n.*405A>C
NM_152871.4:c.*74A>C	NP_690610.1:n.*74A>C
NM_152872.4:c.*394A>C	NP_690611.1:n.*394A>C
NR_028033.4:n.989A>C
NR_028034.4:n.851A>C
NR_028035.4:n.914A>C
NR_028036.4:n.1052A>C
NR_135313.2:n.969A>C
NR_135314.2:n.1248A>C
NR_135315.2:n.1001A>C