Canonical Allele Identifier: CA1926639450

Gene: FAS

Linked Data

• dbSNP Id: rs1848693425
• gnomAD v4: 10-89014484-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014484G>A , CM000672.2:g.89014484G>A	GRCh38
NC_000010.10:g.90774241G>A , CM000672.1:g.90774241G>A	GRCh37
NC_000010.9:g.90764221G>A	NCBI36
NG_009089.2:g.28954G>A , LRG_134:g.28954G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1351G>A
ENST00000355740.8:c.*365G>A	ENSP00000347979.3:n.*365G>A
ENST00000357339.7:c.*34G>A	ENSP00000349896.2:n.*34G>A
ENST00000371857.8:n.2587G>A
ENST00000460510.6:c.*34G>A	ENSP00000512812.1:n.*34G>A
ENST00000466081.6:n.2691G>A
ENST00000477270.6:c.*34G>A	ENSP00000512813.1:n.*34G>A
ENST00000479522.6:c.*471G>A	ENSP00000424113.1:n.*471G>A
ENST00000484444.6:c.*483G>A	ENSP00000420975.1:n.*483G>A
ENST00000488877.6:c.933G>A	ENSP00000425159.1:n.933G>A
ENST00000492756.7:c.*471G>A	ENSP00000422453.1:n.*471G>A
ENST00000494799.6:c.*34G>A	ENSP00000512834.1:n.*34G>A
ENST00000562983.3:c.*34G>A	ENSP00000512845.1:n.*34G>A
ENST00000612663.6:c.*444G>A	ENSP00000477997.3:n.*444G>A
ENST00000640140.2:n.1187G>A
ENST00000640250.2:n.541G>A
ENST00000640681.2:n.1146G>A
ENST00000696723.1:n.4675G>A
ENST00000696741.1:n.2680G>A
ENST00000696742.1:n.2407G>A
ENST00000696743.1:n.3810G>A
ENST00000696744.1:n.1081G>A
ENST00000696767.1:n.1376G>A
ENST00000696768.1:c.*365G>A	ENSP00000512859.1:n.*365G>A
ENST00000696769.1:n.2731G>A
ENST00000696771.1:c.*34G>A	ENSP00000512860.1:n.*34G>A
ENST00000696772.1:n.2645G>A
ENST00000696773.1:n.2384G>A
ENST00000696774.1:n.6152G>A
ENST00000696776.1:c.*34G>A	ENSP00000512861.1:n.*34G>A
ENST00000696777.1:n.2450G>A
ENST00000696778.1:n.1478G>A
ENST00000696779.1:c.*34G>A	ENSP00000512862.1:n.*34G>A
ENST00000696780.1:c.*34G>A	ENSP00000512863.1:n.*34G>A
ENST00000696781.1:c.*34G>A	ENSP00000512864.1:n.*34G>A
ENST00000696782.1:c.*444G>A	ENSP00000512865.1:n.*444G>A
ENST00000696783.1:n.2910G>A
ENST00000696992.1:n.2159G>A
ENST00000696995.1:n.4571G>A
ENST00000696996.1:n.2484G>A
ENST00000696997.1:c.*672G>A	ENSP00000513028.1:n.*672G>A
ENST00000696998.1:n.2296G>A
ENST00000696999.1:c.*34G>A	ENSP00000513029.1:n.*34G>A
ENST00000697036.1:c.*458G>A	ENSP00000513060.1:n.*458G>A
ENST00000697037.1:n.1077G>A
ENST00000697093.1:n.3278G>A
ENST00000697094.1:n.3625G>A
ENST00000697095.1:c.*2243G>A	ENSP00000513104.1:n.*2243G>A
ENST00000697096.1:n.2175G>A
ENST00000697097.1:c.*34G>A	ENSP00000513105.1:n.*34G>A
ENST00000562983.2:n.1228G>A
ENST00000690268.1:c.*34G>A	ENSP00000509810.1:n.*34G>A
ENST00000355740.7:c.*368G>A	ENSP00000347979.3:n.*368G>A
ENST00000640140.1:n.1214G>A
ENST00000640250.1:n.541G>A
ENST00000640681.1:n.1163G>A
ENST00000652046.1:c.*34G>A MANE Select	ENSP00000498466.1:n.*34G>A
ENST00000352159.8:c.*359G>A	ENSP00000345601.4:n.*359G>A
ENST00000355740.6:c.*34G>A	ENSP00000347979.2:n.*34G>A
ENST00000479522.5:c.*471G>A	ENSP00000424113.1:n.*471G>A
ENST00000484444.5:c.*483G>A	ENSP00000420975.1:n.*483G>A
ENST00000494410.5:c.*400G>A	ENSP00000423755.1:n.*400G>A
NM_000043.4:c.*34G>A , LRG_134t1:c.*34G>A	NP_000034.1:n.*34G>A
NM_152871.2:c.*34G>A	NP_690610.1:n.*34G>A
NM_152872.2:c.*354G>A	NP_690611.1:n.*354G>A
NR_028033.2:n.1216G>A
NR_028034.2:n.1078G>A
NR_028035.2:n.1141G>A
NR_028036.2:n.1279G>A
XM_006717819.2:c.*34G>A	XP_006717882.1:n.*34G>A
XM_011539764.1:c.*34G>A	XP_011538066.1:n.*34G>A
XM_011539765.1:c.*34G>A	XP_011538067.1:n.*34G>A
XM_011539766.1:c.*34G>A	XP_011538068.1:n.*34G>A
XM_011539767.1:c.*34G>A	XP_011538069.1:n.*34G>A
XR_945733.1:n.1047G>A
NM_000043.5:c.*34G>A	NP_000034.1:n.*34G>A
NM_001320619.1:c.*365G>A	NP_001307548.1:n.*365G>A
NM_152871.3:c.*34G>A	NP_690610.1:n.*34G>A
NM_152872.3:c.*354G>A	NP_690611.1:n.*354G>A
NR_028033.3:n.1188G>A
NR_028034.3:n.1050G>A
NR_028035.3:n.1113G>A
NR_028036.3:n.1251G>A
NR_135313.1:n.1168G>A
NR_135314.1:n.1351G>A
NR_135315.1:n.1104G>A
XM_006717819.3:c.*34G>A	XP_006717882.1:n.*34G>A
XM_011539764.2:c.*34G>A	XP_011538066.1:n.*34G>A
XM_011539765.2:c.*34G>A	XP_011538067.1:n.*34G>A
XM_011539766.2:c.*34G>A	XP_011538068.1:n.*34G>A
XM_011539767.3:c.*34G>A	XP_011538069.1:n.*34G>A
XR_945732.3:n.1110G>A
XR_945733.2:n.1047G>A
NM_000043.6:c.*34G>A MANE Select	NP_000034.1:n.*34G>A
NM_001320619.2:c.*365G>A	NP_001307548.1:n.*365G>A
NM_152871.4:c.*34G>A	NP_690610.1:n.*34G>A
NM_152872.4:c.*354G>A	NP_690611.1:n.*354G>A
NR_028033.4:n.949G>A
NR_028034.4:n.811G>A
NR_028035.4:n.874G>A
NR_028036.4:n.1012G>A
NR_135313.2:n.929G>A
NR_135314.2:n.1208G>A
NR_135315.2:n.961G>A