Canonical Allele Identifier: CA669680113

Gene: FAS

Linked Data

• dbSNP Id: rs1279526757
• gnomAD v3: 10-89014681-T-C
• gnomAD v4: 10-89014681-T-C
• MyVariant Identifiers: chr10:g.90774438T>C (hg19) ; chr10:g.89014681T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014681T>C , CM000672.2:g.89014681T>C	GRCh38
NC_000010.10:g.90774438T>C , CM000672.1:g.90774438T>C	GRCh37
NC_000010.9:g.90764418T>C	NCBI36
NG_009089.2:g.29151T>C , LRG_134:g.29151T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1548T>C
ENST00000355740.8:c.*562T>C	ENSP00000347979.3:n.*562T>C
ENST00000357339.7:c.*231T>C	ENSP00000349896.2:n.*231T>C
ENST00000371857.8:n.2784T>C
ENST00000460510.6:c.*231T>C	ENSP00000512812.1:n.*231T>C
ENST00000466081.6:n.2888T>C
ENST00000477270.6:c.*231T>C	ENSP00000512813.1:n.*231T>C
ENST00000492756.7:c.*668T>C	ENSP00000422453.1:n.*668T>C
ENST00000494799.6:c.*231T>C	ENSP00000512834.1:n.*231T>C
ENST00000562983.3:c.*231T>C	ENSP00000512845.1:n.*231T>C
ENST00000612663.6:c.*641T>C	ENSP00000477997.3:n.*641T>C
ENST00000640140.2:n.1384T>C
ENST00000640250.2:n.738T>C
ENST00000640681.2:n.1343T>C
ENST00000696723.1:n.4872T>C
ENST00000696741.1:n.2877T>C
ENST00000696742.1:n.2604T>C
ENST00000696743.1:n.4007T>C
ENST00000696744.1:n.1278T>C
ENST00000696767.1:n.1573T>C
ENST00000696768.1:c.*562T>C	ENSP00000512859.1:n.*562T>C
ENST00000696771.1:c.*231T>C	ENSP00000512860.1:n.*231T>C
ENST00000696772.1:n.2842T>C
ENST00000696773.1:n.2581T>C
ENST00000696774.1:n.6349T>C
ENST00000696776.1:c.*231T>C	ENSP00000512861.1:n.*231T>C
ENST00000696777.1:n.2647T>C
ENST00000696778.1:n.1675T>C
ENST00000696779.1:c.*231T>C	ENSP00000512862.1:n.*231T>C
ENST00000696780.1:c.*231T>C	ENSP00000512863.1:n.*231T>C
ENST00000696781.1:c.*231T>C	ENSP00000512864.1:n.*231T>C
ENST00000696782.1:c.*641T>C	ENSP00000512865.1:n.*641T>C
ENST00000696783.1:n.3107T>C
ENST00000696992.1:n.2356T>C
ENST00000696995.1:n.4768T>C
ENST00000696996.1:n.2681T>C
ENST00000696997.1:c.*869T>C	ENSP00000513028.1:n.*869T>C
ENST00000696998.1:n.2493T>C
ENST00000696999.1:c.*231T>C	ENSP00000513029.1:n.*231T>C
ENST00000697036.1:c.*655T>C	ENSP00000513060.1:n.*655T>C
ENST00000697037.1:n.1274T>C
ENST00000697093.1:n.3475T>C
ENST00000697094.1:n.3822T>C
ENST00000697095.1:c.*2440T>C	ENSP00000513104.1:n.*2440T>C
ENST00000697096.1:n.2372T>C
ENST00000697097.1:c.*231T>C	ENSP00000513105.1:n.*231T>C
ENST00000562983.2:n.1425T>C
ENST00000690268.1:c.*231T>C	ENSP00000509810.1:n.*231T>C
ENST00000355740.7:c.*565T>C	ENSP00000347979.3:n.*565T>C
ENST00000640140.1:n.1411T>C
ENST00000640250.1:n.738T>C
ENST00000640681.1:n.1360T>C
ENST00000652046.1:c.*231T>C MANE Select	ENSP00000498466.1:n.*231T>C
ENST00000352159.8:c.*556T>C	ENSP00000345601.4:n.*556T>C
ENST00000355740.6:c.*231T>C	ENSP00000347979.2:n.*231T>C
NM_000043.4:c.*231T>C , LRG_134t1:c.*231T>C	NP_000034.1:n.*231T>C
NM_152871.2:c.*231T>C	NP_690610.1:n.*231T>C
NM_152872.2:c.*551T>C	NP_690611.1:n.*551T>C
NR_028033.2:n.1413T>C
NR_028034.2:n.1275T>C
NR_028035.2:n.1338T>C
NR_028036.2:n.1476T>C
XM_006717819.2:c.*231T>C	XP_006717882.1:n.*231T>C
XM_011539764.1:c.*231T>C	XP_011538066.1:n.*231T>C
XM_011539765.1:c.*231T>C	XP_011538067.1:n.*231T>C
XM_011539766.1:c.*231T>C	XP_011538068.1:n.*231T>C
XM_011539767.1:c.*231T>C	XP_011538069.1:n.*231T>C
NM_000043.5:c.*231T>C	NP_000034.1:n.*231T>C
NM_001320619.1:c.*562T>C	NP_001307548.1:n.*562T>C
NM_152871.3:c.*231T>C	NP_690610.1:n.*231T>C
NM_152872.3:c.*551T>C	NP_690611.1:n.*551T>C
NR_028033.3:n.1385T>C
NR_028034.3:n.1247T>C
NR_028035.3:n.1310T>C
NR_028036.3:n.1448T>C
NR_135313.1:n.1365T>C
NR_135314.1:n.1548T>C
NR_135315.1:n.1301T>C
XM_006717819.3:c.*231T>C	XP_006717882.1:n.*231T>C
XM_011539764.2:c.*231T>C	XP_011538066.1:n.*231T>C
XM_011539765.2:c.*231T>C	XP_011538067.1:n.*231T>C
XM_011539766.2:c.*231T>C	XP_011538068.1:n.*231T>C
XM_011539767.3:c.*231T>C	XP_011538069.1:n.*231T>C
XR_945732.3:n.1307T>C
XR_945733.2:n.1244T>C
NM_000043.6:c.*231T>C MANE Select	NP_000034.1:n.*231T>C
NM_001320619.2:c.*562T>C	NP_001307548.1:n.*562T>C
NM_152871.4:c.*231T>C	NP_690610.1:n.*231T>C
NM_152872.4:c.*551T>C	NP_690611.1:n.*551T>C
NR_028033.4:n.1146T>C
NR_028034.4:n.1008T>C
NR_028035.4:n.1071T>C
NR_028036.4:n.1209T>C
NR_135313.2:n.1126T>C
NR_135314.2:n.1405T>C
NR_135315.2:n.1158T>C