Canonical Allele Identifier: CA594943256

Gene: FAS

Linked Data

• dbSNP Id: rs1376818939
• gnomAD v2: 10-90774334-C-T
• gnomAD v4: 10-89014577-C-T
• MyVariant Identifiers: chr10:g.90774334C>T (hg19) ; chr10:g.89014577C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014577C>T , CM000672.2:g.89014577C>T	GRCh38
NC_000010.10:g.90774334C>T , CM000672.1:g.90774334C>T	GRCh37
NC_000010.9:g.90764314C>T	NCBI36
NG_009089.2:g.29047C>T , LRG_134:g.29047C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1444C>T
ENST00000355740.8:c.*458C>T	ENSP00000347979.3:n.*458C>T
ENST00000357339.7:c.*127C>T	ENSP00000349896.2:n.*127C>T
ENST00000371857.8:n.2680C>T
ENST00000460510.6:c.*127C>T	ENSP00000512812.1:n.*127C>T
ENST00000466081.6:n.2784C>T
ENST00000477270.6:c.*127C>T	ENSP00000512813.1:n.*127C>T
ENST00000479522.6:c.*564C>T	ENSP00000424113.1:n.*564C>T
ENST00000484444.6:c.*576C>T	ENSP00000420975.1:n.*576C>T
ENST00000488877.6:c.1026C>T	ENSP00000425159.1:n.1026C>T
ENST00000492756.7:c.*564C>T	ENSP00000422453.1:n.*564C>T
ENST00000494799.6:c.*127C>T	ENSP00000512834.1:n.*127C>T
ENST00000562983.3:c.*127C>T	ENSP00000512845.1:n.*127C>T
ENST00000612663.6:c.*537C>T	ENSP00000477997.3:n.*537C>T
ENST00000640140.2:n.1280C>T
ENST00000640250.2:n.634C>T
ENST00000640681.2:n.1239C>T
ENST00000696723.1:n.4768C>T
ENST00000696741.1:n.2773C>T
ENST00000696742.1:n.2500C>T
ENST00000696743.1:n.3903C>T
ENST00000696744.1:n.1174C>T
ENST00000696767.1:n.1469C>T
ENST00000696768.1:c.*458C>T	ENSP00000512859.1:n.*458C>T
ENST00000696771.1:c.*127C>T	ENSP00000512860.1:n.*127C>T
ENST00000696772.1:n.2738C>T
ENST00000696773.1:n.2477C>T
ENST00000696774.1:n.6245C>T
ENST00000696776.1:c.*127C>T	ENSP00000512861.1:n.*127C>T
ENST00000696777.1:n.2543C>T
ENST00000696778.1:n.1571C>T
ENST00000696779.1:c.*127C>T	ENSP00000512862.1:n.*127C>T
ENST00000696780.1:c.*127C>T	ENSP00000512863.1:n.*127C>T
ENST00000696781.1:c.*127C>T	ENSP00000512864.1:n.*127C>T
ENST00000696782.1:c.*537C>T	ENSP00000512865.1:n.*537C>T
ENST00000696783.1:n.3003C>T
ENST00000696992.1:n.2252C>T
ENST00000696995.1:n.4664C>T
ENST00000696996.1:n.2577C>T
ENST00000696997.1:c.*765C>T	ENSP00000513028.1:n.*765C>T
ENST00000696998.1:n.2389C>T
ENST00000696999.1:c.*127C>T	ENSP00000513029.1:n.*127C>T
ENST00000697036.1:c.*551C>T	ENSP00000513060.1:n.*551C>T
ENST00000697037.1:n.1170C>T
ENST00000697093.1:n.3371C>T
ENST00000697094.1:n.3718C>T
ENST00000697095.1:c.*2336C>T	ENSP00000513104.1:n.*2336C>T
ENST00000697096.1:n.2268C>T
ENST00000697097.1:c.*127C>T	ENSP00000513105.1:n.*127C>T
ENST00000562983.2:n.1321C>T
ENST00000690268.1:c.*127C>T	ENSP00000509810.1:n.*127C>T
ENST00000355740.7:c.*461C>T	ENSP00000347979.3:n.*461C>T
ENST00000640140.1:n.1307C>T
ENST00000640250.1:n.634C>T
ENST00000640681.1:n.1256C>T
ENST00000652046.1:c.*127C>T MANE Select	ENSP00000498466.1:n.*127C>T
ENST00000352159.8:c.*452C>T	ENSP00000345601.4:n.*452C>T
ENST00000355740.6:c.*127C>T	ENSP00000347979.2:n.*127C>T
ENST00000479522.5:c.*564C>T	ENSP00000424113.1:n.*564C>T
ENST00000484444.5:c.*576C>T	ENSP00000420975.1:n.*576C>T
ENST00000494410.5:c.*493C>T	ENSP00000423755.1:n.*493C>T
NM_000043.4:c.*127C>T , LRG_134t1:c.*127C>T	NP_000034.1:n.*127C>T
NM_152871.2:c.*127C>T	NP_690610.1:n.*127C>T
NM_152872.2:c.*447C>T	NP_690611.1:n.*447C>T
NR_028033.2:n.1309C>T
NR_028034.2:n.1171C>T
NR_028035.2:n.1234C>T
NR_028036.2:n.1372C>T
XM_006717819.2:c.*127C>T	XP_006717882.1:n.*127C>T
XM_011539764.1:c.*127C>T	XP_011538066.1:n.*127C>T
XM_011539765.1:c.*127C>T	XP_011538067.1:n.*127C>T
XM_011539766.1:c.*127C>T	XP_011538068.1:n.*127C>T
XM_011539767.1:c.*127C>T	XP_011538069.1:n.*127C>T
NM_000043.5:c.*127C>T	NP_000034.1:n.*127C>T
NM_001320619.1:c.*458C>T	NP_001307548.1:n.*458C>T
NM_152871.3:c.*127C>T	NP_690610.1:n.*127C>T
NM_152872.3:c.*447C>T	NP_690611.1:n.*447C>T
NR_028033.3:n.1281C>T
NR_028034.3:n.1143C>T
NR_028035.3:n.1206C>T
NR_028036.3:n.1344C>T
NR_135313.1:n.1261C>T
NR_135314.1:n.1444C>T
NR_135315.1:n.1197C>T
XM_006717819.3:c.*127C>T	XP_006717882.1:n.*127C>T
XM_011539764.2:c.*127C>T	XP_011538066.1:n.*127C>T
XM_011539765.2:c.*127C>T	XP_011538067.1:n.*127C>T
XM_011539766.2:c.*127C>T	XP_011538068.1:n.*127C>T
XM_011539767.3:c.*127C>T	XP_011538069.1:n.*127C>T
XR_945732.3:n.1203C>T
XR_945733.2:n.1140C>T
NM_000043.6:c.*127C>T MANE Select	NP_000034.1:n.*127C>T
NM_001320619.2:c.*458C>T	NP_001307548.1:n.*458C>T
NM_152871.4:c.*127C>T	NP_690610.1:n.*127C>T
NM_152872.4:c.*447C>T	NP_690611.1:n.*447C>T
NR_028033.4:n.1042C>T
NR_028034.4:n.904C>T
NR_028035.4:n.967C>T
NR_028036.4:n.1105C>T
NR_135313.2:n.1022C>T
NR_135314.2:n.1301C>T
NR_135315.2:n.1054C>T