Canonical Allele Identifier: CA10629425

Gene: FAS

Linked Data

• ClinVar Variation Id: 301533
• ClinVar RCV Id: RCV000297614
• dbSNP Id: rs886047461
• gnomAD v4: 10-89014538-T-C
• MyVariant Identifiers: chr10:g.90774295T>C (hg19) ; chr10:g.89014538T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014538T>C , CM000672.2:g.89014538T>C	GRCh38
NC_000010.10:g.90774295T>C , CM000672.1:g.90774295T>C	GRCh37
NC_000010.9:g.90764275T>C	NCBI36
NG_009089.2:g.29008T>C , LRG_134:g.29008T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1405T>C
ENST00000355740.8:c.*419T>C	ENSP00000347979.3:n.*419T>C
ENST00000357339.7:c.*88T>C	ENSP00000349896.2:n.*88T>C
ENST00000371857.8:n.2641T>C
ENST00000460510.6:c.*88T>C	ENSP00000512812.1:n.*88T>C
ENST00000466081.6:n.2745T>C
ENST00000477270.6:c.*88T>C	ENSP00000512813.1:n.*88T>C
ENST00000479522.6:c.*525T>C	ENSP00000424113.1:n.*525T>C
ENST00000484444.6:c.*537T>C	ENSP00000420975.1:n.*537T>C
ENST00000488877.6:c.987T>C	ENSP00000425159.1:n.987T>C
ENST00000492756.7:c.*525T>C	ENSP00000422453.1:n.*525T>C
ENST00000494799.6:c.*88T>C	ENSP00000512834.1:n.*88T>C
ENST00000562983.3:c.*88T>C	ENSP00000512845.1:n.*88T>C
ENST00000612663.6:c.*498T>C	ENSP00000477997.3:n.*498T>C
ENST00000640140.2:n.1241T>C
ENST00000640250.2:n.595T>C
ENST00000640681.2:n.1200T>C
ENST00000696723.1:n.4729T>C
ENST00000696741.1:n.2734T>C
ENST00000696742.1:n.2461T>C
ENST00000696743.1:n.3864T>C
ENST00000696744.1:n.1135T>C
ENST00000696767.1:n.1430T>C
ENST00000696768.1:c.*419T>C	ENSP00000512859.1:n.*419T>C
ENST00000696769.1:n.2785T>C
ENST00000696771.1:c.*88T>C	ENSP00000512860.1:n.*88T>C
ENST00000696772.1:n.2699T>C
ENST00000696773.1:n.2438T>C
ENST00000696774.1:n.6206T>C
ENST00000696776.1:c.*88T>C	ENSP00000512861.1:n.*88T>C
ENST00000696777.1:n.2504T>C
ENST00000696778.1:n.1532T>C
ENST00000696779.1:c.*88T>C	ENSP00000512862.1:n.*88T>C
ENST00000696780.1:c.*88T>C	ENSP00000512863.1:n.*88T>C
ENST00000696781.1:c.*88T>C	ENSP00000512864.1:n.*88T>C
ENST00000696782.1:c.*498T>C	ENSP00000512865.1:n.*498T>C
ENST00000696783.1:n.2964T>C
ENST00000696992.1:n.2213T>C
ENST00000696995.1:n.4625T>C
ENST00000696996.1:n.2538T>C
ENST00000696997.1:c.*726T>C	ENSP00000513028.1:n.*726T>C
ENST00000696998.1:n.2350T>C
ENST00000696999.1:c.*88T>C	ENSP00000513029.1:n.*88T>C
ENST00000697036.1:c.*512T>C	ENSP00000513060.1:n.*512T>C
ENST00000697037.1:n.1131T>C
ENST00000697093.1:n.3332T>C
ENST00000697094.1:n.3679T>C
ENST00000697095.1:c.*2297T>C	ENSP00000513104.1:n.*2297T>C
ENST00000697096.1:n.2229T>C
ENST00000697097.1:c.*88T>C	ENSP00000513105.1:n.*88T>C
ENST00000562983.2:n.1282T>C
ENST00000690268.1:c.*88T>C	ENSP00000509810.1:n.*88T>C
ENST00000355740.7:c.*422T>C	ENSP00000347979.3:n.*422T>C
ENST00000640140.1:n.1268T>C
ENST00000640250.1:n.595T>C
ENST00000640681.1:n.1217T>C
ENST00000652046.1:c.*88T>C MANE Select	ENSP00000498466.1:n.*88T>C
ENST00000352159.8:c.*413T>C	ENSP00000345601.4:n.*413T>C
ENST00000355740.6:c.*88T>C	ENSP00000347979.2:n.*88T>C
ENST00000479522.5:c.*525T>C	ENSP00000424113.1:n.*525T>C
ENST00000484444.5:c.*537T>C	ENSP00000420975.1:n.*537T>C
ENST00000494410.5:c.*454T>C	ENSP00000423755.1:n.*454T>C
NM_000043.4:c.*88T>C , LRG_134t1:c.*88T>C	NP_000034.1:n.*88T>C
NM_152871.2:c.*88T>C	NP_690610.1:n.*88T>C
NM_152872.2:c.*408T>C	NP_690611.1:n.*408T>C
NR_028033.2:n.1270T>C
NR_028034.2:n.1132T>C
NR_028035.2:n.1195T>C
NR_028036.2:n.1333T>C
XM_006717819.2:c.*88T>C	XP_006717882.1:n.*88T>C
XM_011539764.1:c.*88T>C	XP_011538066.1:n.*88T>C
XM_011539765.1:c.*88T>C	XP_011538067.1:n.*88T>C
XM_011539766.1:c.*88T>C	XP_011538068.1:n.*88T>C
XM_011539767.1:c.*88T>C	XP_011538069.1:n.*88T>C
NM_000043.5:c.*88T>C	NP_000034.1:n.*88T>C
NM_001320619.1:c.*419T>C	NP_001307548.1:n.*419T>C
NM_152871.3:c.*88T>C	NP_690610.1:n.*88T>C
NM_152872.3:c.*408T>C	NP_690611.1:n.*408T>C
NR_028033.3:n.1242T>C
NR_028034.3:n.1104T>C
NR_028035.3:n.1167T>C
NR_028036.3:n.1305T>C
NR_135313.1:n.1222T>C
NR_135314.1:n.1405T>C
NR_135315.1:n.1158T>C
XM_006717819.3:c.*88T>C	XP_006717882.1:n.*88T>C
XM_011539764.2:c.*88T>C	XP_011538066.1:n.*88T>C
XM_011539765.2:c.*88T>C	XP_011538067.1:n.*88T>C
XM_011539766.2:c.*88T>C	XP_011538068.1:n.*88T>C
XM_011539767.3:c.*88T>C	XP_011538069.1:n.*88T>C
XR_945732.3:n.1164T>C
XR_945733.2:n.1101T>C
NM_000043.6:c.*88T>C MANE Select	NP_000034.1:n.*88T>C
NM_001320619.2:c.*419T>C	NP_001307548.1:n.*419T>C
NM_152871.4:c.*88T>C	NP_690610.1:n.*88T>C
NM_152872.4:c.*408T>C	NP_690611.1:n.*408T>C
NR_028033.4:n.1003T>C
NR_028034.4:n.865T>C
NR_028035.4:n.928T>C
NR_028036.4:n.1066T>C
NR_135313.2:n.983T>C
NR_135314.2:n.1262T>C
NR_135315.2:n.1015T>C