Canonical Allele Identifier: CA377510080

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774104A>T (hg19) ; chr10:g.89014347A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014347A>T , CM000672.2:g.89014347A>T	GRCh38
NC_000010.10:g.90774104A>T , CM000672.1:g.90774104A>T	GRCh37
NC_000010.9:g.90764084A>T	NCBI36
NG_009089.2:g.28817A>T , LRG_134:g.28817A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1214A>T
ENST00000355740.8:c.*228A>T	ENSP00000347979.3:n.*228A>T
ENST00000357339.7:c.842A>T	ENSP00000349896.2:p.Asn281Ile
ENST00000371857.8:n.2450A>T
ENST00000460510.6:c.188A>T	ENSP00000512812.1:p.Asn63Ile
ENST00000466081.6:n.2554A>T
ENST00000477270.6:c.950A>T	ENSP00000512813.1:p.Asn317Ile
ENST00000479522.6:c.*334A>T	ENSP00000424113.1:n.*334A>T
ENST00000484444.6:c.*346A>T	ENSP00000420975.1:n.*346A>T
ENST00000488877.6:c.796A>T	ENSP00000425159.1:n.796A>T
ENST00000492756.7:c.*334A>T	ENSP00000422453.1:n.*334A>T
ENST00000494799.6:c.188A>T	ENSP00000512834.1:p.Asn63Ile
ENST00000562983.3:c.188A>T	ENSP00000512845.1:p.Asn63Ile
ENST00000612663.6:c.*307A>T	ENSP00000477997.3:n.*307A>T
ENST00000640140.2:n.1050A>T
ENST00000640250.2:n.404A>T
ENST00000640681.2:n.1009A>T
ENST00000696723.1:n.4538A>T
ENST00000696741.1:n.2543A>T
ENST00000696742.1:n.2270A>T
ENST00000696743.1:n.3673A>T
ENST00000696744.1:n.944A>T
ENST00000696767.1:n.1239A>T
ENST00000696768.1:c.*228A>T	ENSP00000512859.1:n.*228A>T
ENST00000696769.1:n.2594A>T
ENST00000696771.1:c.188A>T	ENSP00000512860.1:p.Asn63Ile
ENST00000696772.1:n.2508A>T
ENST00000696773.1:n.2247A>T
ENST00000696774.1:n.6015A>T
ENST00000696776.1:c.998A>T	ENSP00000512861.1:p.Asn333Ile
ENST00000696777.1:n.2313A>T
ENST00000696778.1:n.1341A>T
ENST00000696779.1:c.512A>T	ENSP00000512862.1:p.Asn171Ile
ENST00000696780.1:c.935A>T	ENSP00000512863.1:p.Asn312Ile
ENST00000696781.1:c.650A>T	ENSP00000512864.1:p.Asn217Ile
ENST00000696782.1:c.*307A>T	ENSP00000512865.1:n.*307A>T
ENST00000696783.1:n.2773A>T
ENST00000696992.1:n.2022A>T
ENST00000696995.1:n.4434A>T
ENST00000696996.1:n.2347A>T
ENST00000696997.1:c.*535A>T	ENSP00000513028.1:n.*535A>T
ENST00000696998.1:n.2159A>T
ENST00000696999.1:c.188A>T	ENSP00000513029.1:p.Asn63Ile
ENST00000697036.1:c.*321A>T	ENSP00000513060.1:n.*321A>T
ENST00000697037.1:n.940A>T
ENST00000697093.1:n.3141A>T
ENST00000697094.1:n.3488A>T
ENST00000697095.1:c.*2106A>T	ENSP00000513104.1:n.*2106A>T
ENST00000697096.1:n.2038A>T
ENST00000697097.1:c.188A>T	ENSP00000513105.1:p.Asn63Ile
ENST00000562983.2:n.1091A>T
ENST00000690268.1:c.986A>T	ENSP00000509810.1:p.Asn329Ile
ENST00000355740.7:c.*231A>T	ENSP00000347979.3:n.*231A>T
ENST00000612663.5:c.*307A>T	ENSP00000477997.3:n.*307A>T
ENST00000640140.1:n.1077A>T
ENST00000640250.1:n.404A>T
ENST00000640681.1:n.1026A>T
ENST00000652046.1:c.905A>T MANE Select	ENSP00000498466.1:p.Asn302Ile
ENST00000352159.8:c.*222A>T	ENSP00000345601.4:n.*222A>T
ENST00000355279.2:c.880A>T	ENSP00000347426.2:n.880A>T
ENST00000355740.6:c.905A>T	ENSP00000347979.2:p.Asn302Ile
ENST00000357339.6:c.842A>T	ENSP00000349896.2:p.Asn281Ile
ENST00000479522.5:c.*334A>T	ENSP00000424113.1:n.*334A>T
ENST00000484444.5:c.*346A>T	ENSP00000420975.1:n.*346A>T
ENST00000488877.5:c.*346A>T	ENSP00000425159.1:n.*346A>T
ENST00000492756.5:c.733A>T	ENSP00000422453.1:n.733A>T
ENST00000494410.5:c.*263A>T	ENSP00000423755.1:n.*263A>T
ENST00000612663.4:c.*252A>T	ENSP00000477997.2:n.*252A>T
NM_000043.4:c.905A>T , LRG_134t1:c.905A>T	NP_000034.1:p.Asn302Ile
NM_152871.2:c.842A>T	NP_690610.1:p.Asn281Ile
NM_152872.2:c.*217A>T	NP_690611.1:n.*217A>T
NR_028033.2:n.1079A>T
NR_028034.2:n.941A>T
NR_028035.2:n.1004A>T
NR_028036.2:n.1142A>T
XM_006717819.2:c.986A>T	XP_006717882.1:p.Asn329Ile
XM_011539764.1:c.1067A>T	XP_011538066.1:p.Asn356Ile
XM_011539765.1:c.1004A>T	XP_011538067.1:p.Asn335Ile
XM_011539766.1:c.986A>T	XP_011538068.1:p.Asn329Ile
XM_011539767.1:c.950A>T	XP_011538069.1:p.Asn317Ile
XR_945732.1:n.973A>T
XR_945733.1:n.910A>T
NM_000043.5:c.905A>T	NP_000034.1:p.Asn302Ile
NM_001320619.1:c.*228A>T	NP_001307548.1:n.*228A>T
NM_152871.3:c.842A>T	NP_690610.1:p.Asn281Ile
NM_152872.3:c.*217A>T	NP_690611.1:n.*217A>T
NR_028033.3:n.1051A>T
NR_028034.3:n.913A>T
NR_028035.3:n.976A>T
NR_028036.3:n.1114A>T
NR_135313.1:n.1031A>T
NR_135314.1:n.1214A>T
NR_135315.1:n.967A>T
XM_006717819.3:c.986A>T	XP_006717882.1:p.Asn329Ile
XM_011539764.2:c.1067A>T	XP_011538066.1:p.Asn356Ile
XM_011539765.2:c.1004A>T	XP_011538067.1:p.Asn335Ile
XM_011539766.2:c.986A>T	XP_011538068.1:p.Asn329Ile
XM_011539767.3:c.950A>T	XP_011538069.1:p.Asn317Ile
XR_945732.3:n.973A>T
XR_945733.2:n.910A>T
NM_000043.6:c.905A>T MANE Select	NP_000034.1:p.Asn302Ile
NM_001320619.2:c.*228A>T	NP_001307548.1:n.*228A>T
NM_152871.4:c.842A>T	NP_690610.1:p.Asn281Ile
NM_152872.4:c.*217A>T	NP_690611.1:n.*217A>T
NR_028033.4:n.812A>T
NR_028034.4:n.674A>T
NR_028035.4:n.737A>T
NR_028036.4:n.875A>T
NR_135313.2:n.792A>T
NR_135314.2:n.1071A>T
NR_135315.2:n.824A>T