Canonical Allele Identifier: CA377510091

Gene: FAS

Linked Data

• dbSNP Id: rs1275805220
• gnomAD v2: 10-90774109-T-A
• MyVariant Identifiers: chr10:g.90774109T>A (hg19) ; chr10:g.89014352T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014352T>A , CM000672.2:g.89014352T>A	GRCh38
NC_000010.10:g.90774109T>A , CM000672.1:g.90774109T>A	GRCh37
NC_000010.9:g.90764089T>A	NCBI36
NG_009089.2:g.28822T>A , LRG_134:g.28822T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1219T>A
ENST00000355740.8:c.*233T>A	ENSP00000347979.3:n.*233T>A
ENST00000357339.7:c.847T>A	ENSP00000349896.2:p.Cys283Ser
ENST00000371857.8:n.2455T>A
ENST00000460510.6:c.193T>A	ENSP00000512812.1:p.Cys65Ser
ENST00000466081.6:n.2559T>A
ENST00000477270.6:c.955T>A	ENSP00000512813.1:p.Cys319Ser
ENST00000479522.6:c.*339T>A	ENSP00000424113.1:n.*339T>A
ENST00000484444.6:c.*351T>A	ENSP00000420975.1:n.*351T>A
ENST00000488877.6:c.801T>A	ENSP00000425159.1:n.801T>A
ENST00000492756.7:c.*339T>A	ENSP00000422453.1:n.*339T>A
ENST00000494799.6:c.193T>A	ENSP00000512834.1:p.Cys65Ser
ENST00000562983.3:c.193T>A	ENSP00000512845.1:p.Cys65Ser
ENST00000612663.6:c.*312T>A	ENSP00000477997.3:n.*312T>A
ENST00000640140.2:n.1055T>A
ENST00000640250.2:n.409T>A
ENST00000640681.2:n.1014T>A
ENST00000696723.1:n.4543T>A
ENST00000696741.1:n.2548T>A
ENST00000696742.1:n.2275T>A
ENST00000696743.1:n.3678T>A
ENST00000696744.1:n.949T>A
ENST00000696767.1:n.1244T>A
ENST00000696768.1:c.*233T>A	ENSP00000512859.1:n.*233T>A
ENST00000696769.1:n.2599T>A
ENST00000696771.1:c.193T>A	ENSP00000512860.1:p.Cys65Ser
ENST00000696772.1:n.2513T>A
ENST00000696773.1:n.2252T>A
ENST00000696774.1:n.6020T>A
ENST00000696776.1:c.1003T>A	ENSP00000512861.1:p.Cys335Ser
ENST00000696777.1:n.2318T>A
ENST00000696778.1:n.1346T>A
ENST00000696779.1:c.517T>A	ENSP00000512862.1:p.Cys173Ser
ENST00000696780.1:c.940T>A	ENSP00000512863.1:p.Cys314Ser
ENST00000696781.1:c.655T>A	ENSP00000512864.1:p.Cys219Ser
ENST00000696782.1:c.*312T>A	ENSP00000512865.1:n.*312T>A
ENST00000696783.1:n.2778T>A
ENST00000696992.1:n.2027T>A
ENST00000696995.1:n.4439T>A
ENST00000696996.1:n.2352T>A
ENST00000696997.1:c.*540T>A	ENSP00000513028.1:n.*540T>A
ENST00000696998.1:n.2164T>A
ENST00000696999.1:c.193T>A	ENSP00000513029.1:p.Cys65Ser
ENST00000697036.1:c.*326T>A	ENSP00000513060.1:n.*326T>A
ENST00000697037.1:n.945T>A
ENST00000697093.1:n.3146T>A
ENST00000697094.1:n.3493T>A
ENST00000697095.1:c.*2111T>A	ENSP00000513104.1:n.*2111T>A
ENST00000697096.1:n.2043T>A
ENST00000697097.1:c.193T>A	ENSP00000513105.1:p.Cys65Ser
ENST00000562983.2:n.1096T>A
ENST00000690268.1:c.991T>A	ENSP00000509810.1:p.Cys331Ser
ENST00000355740.7:c.*236T>A	ENSP00000347979.3:n.*236T>A
ENST00000612663.5:c.*312T>A	ENSP00000477997.3:n.*312T>A
ENST00000640140.1:n.1082T>A
ENST00000640250.1:n.409T>A
ENST00000640681.1:n.1031T>A
ENST00000652046.1:c.910T>A MANE Select	ENSP00000498466.1:p.Cys304Ser
ENST00000352159.8:c.*227T>A	ENSP00000345601.4:n.*227T>A
ENST00000355279.2:c.885T>A	ENSP00000347426.2:n.885T>A
ENST00000355740.6:c.910T>A	ENSP00000347979.2:p.Cys304Ser
ENST00000357339.6:c.847T>A	ENSP00000349896.2:p.Cys283Ser
ENST00000479522.5:c.*339T>A	ENSP00000424113.1:n.*339T>A
ENST00000484444.5:c.*351T>A	ENSP00000420975.1:n.*351T>A
ENST00000488877.5:c.*351T>A	ENSP00000425159.1:n.*351T>A
ENST00000492756.5:c.738T>A	ENSP00000422453.1:n.738T>A
ENST00000494410.5:c.*268T>A	ENSP00000423755.1:n.*268T>A
ENST00000612663.4:c.*257T>A	ENSP00000477997.2:n.*257T>A
NM_000043.4:c.910T>A , LRG_134t1:c.910T>A	NP_000034.1:p.Cys304Ser
NM_152871.2:c.847T>A	NP_690610.1:p.Cys283Ser
NM_152872.2:c.*222T>A	NP_690611.1:n.*222T>A
NR_028033.2:n.1084T>A
NR_028034.2:n.946T>A
NR_028035.2:n.1009T>A
NR_028036.2:n.1147T>A
XM_006717819.2:c.991T>A	XP_006717882.1:p.Cys331Ser
XM_011539764.1:c.1072T>A	XP_011538066.1:p.Cys358Ser
XM_011539765.1:c.1009T>A	XP_011538067.1:p.Cys337Ser
XM_011539766.1:c.991T>A	XP_011538068.1:p.Cys331Ser
XM_011539767.1:c.955T>A	XP_011538069.1:p.Cys319Ser
XR_945732.1:n.978T>A
XR_945733.1:n.915T>A
NM_000043.5:c.910T>A	NP_000034.1:p.Cys304Ser
NM_001320619.1:c.*233T>A	NP_001307548.1:n.*233T>A
NM_152871.3:c.847T>A	NP_690610.1:p.Cys283Ser
NM_152872.3:c.*222T>A	NP_690611.1:n.*222T>A
NR_028033.3:n.1056T>A
NR_028034.3:n.918T>A
NR_028035.3:n.981T>A
NR_028036.3:n.1119T>A
NR_135313.1:n.1036T>A
NR_135314.1:n.1219T>A
NR_135315.1:n.972T>A
XM_006717819.3:c.991T>A	XP_006717882.1:p.Cys331Ser
XM_011539764.2:c.1072T>A	XP_011538066.1:p.Cys358Ser
XM_011539765.2:c.1009T>A	XP_011538067.1:p.Cys337Ser
XM_011539766.2:c.991T>A	XP_011538068.1:p.Cys331Ser
XM_011539767.3:c.955T>A	XP_011538069.1:p.Cys319Ser
XR_945732.3:n.978T>A
XR_945733.2:n.915T>A
NM_000043.6:c.910T>A MANE Select	NP_000034.1:p.Cys304Ser
NM_001320619.2:c.*233T>A	NP_001307548.1:n.*233T>A
NM_152871.4:c.847T>A	NP_690610.1:p.Cys283Ser
NM_152872.4:c.*222T>A	NP_690611.1:n.*222T>A
NR_028033.4:n.817T>A
NR_028034.4:n.679T>A
NR_028035.4:n.742T>A
NR_028036.4:n.880T>A
NR_135313.2:n.797T>A
NR_135314.2:n.1076T>A
NR_135315.2:n.829T>A