Canonical Allele Identifier: CA377510036

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774085A>C (hg19) ; chr10:g.89014328A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014328A>C , CM000672.2:g.89014328A>C	GRCh38
NC_000010.10:g.90774085A>C , CM000672.1:g.90774085A>C	GRCh37
NC_000010.9:g.90764065A>C	NCBI36
NG_009089.2:g.28798A>C , LRG_134:g.28798A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1195A>C
ENST00000355740.8:c.*209A>C	ENSP00000347979.3:n.*209A>C
ENST00000357339.7:c.823A>C	ENSP00000349896.2:p.Lys275Gln
ENST00000371857.8:n.2431A>C
ENST00000460510.6:c.169A>C	ENSP00000512812.1:p.Lys57Gln
ENST00000466081.6:n.2535A>C
ENST00000477270.6:c.931A>C	ENSP00000512813.1:p.Lys311Gln
ENST00000479522.6:c.*315A>C	ENSP00000424113.1:n.*315A>C
ENST00000484444.6:c.*327A>C	ENSP00000420975.1:n.*327A>C
ENST00000488877.6:c.777A>C	ENSP00000425159.1:n.777A>C
ENST00000492756.7:c.*315A>C	ENSP00000422453.1:n.*315A>C
ENST00000494799.6:c.169A>C	ENSP00000512834.1:p.Lys57Gln
ENST00000562983.3:c.169A>C	ENSP00000512845.1:p.Lys57Gln
ENST00000612663.6:c.*288A>C	ENSP00000477997.3:n.*288A>C
ENST00000640140.2:n.1031A>C
ENST00000640250.2:n.385A>C
ENST00000640681.2:n.990A>C
ENST00000696723.1:n.4519A>C
ENST00000696741.1:n.2524A>C
ENST00000696742.1:n.2251A>C
ENST00000696743.1:n.3654A>C
ENST00000696744.1:n.925A>C
ENST00000696767.1:n.1220A>C
ENST00000696768.1:c.*209A>C	ENSP00000512859.1:n.*209A>C
ENST00000696769.1:n.2575A>C
ENST00000696771.1:c.169A>C	ENSP00000512860.1:p.Lys57Gln
ENST00000696772.1:n.2489A>C
ENST00000696773.1:n.2228A>C
ENST00000696774.1:n.5996A>C
ENST00000696776.1:c.979A>C	ENSP00000512861.1:p.Lys327Gln
ENST00000696777.1:n.2294A>C
ENST00000696778.1:n.1322A>C
ENST00000696779.1:c.493A>C	ENSP00000512862.1:p.Lys165Gln
ENST00000696780.1:c.916A>C	ENSP00000512863.1:p.Lys306Gln
ENST00000696781.1:c.631A>C	ENSP00000512864.1:p.Lys211Gln
ENST00000696782.1:c.*288A>C	ENSP00000512865.1:n.*288A>C
ENST00000696783.1:n.2754A>C
ENST00000696992.1:n.2003A>C
ENST00000696995.1:n.4415A>C
ENST00000696996.1:n.2328A>C
ENST00000696997.1:c.*516A>C	ENSP00000513028.1:n.*516A>C
ENST00000696998.1:n.2140A>C
ENST00000696999.1:c.169A>C	ENSP00000513029.1:p.Lys57Gln
ENST00000697036.1:c.*302A>C	ENSP00000513060.1:n.*302A>C
ENST00000697037.1:n.921A>C
ENST00000697093.1:n.3122A>C
ENST00000697094.1:n.3469A>C
ENST00000697095.1:c.*2087A>C	ENSP00000513104.1:n.*2087A>C
ENST00000697096.1:n.2019A>C
ENST00000697097.1:c.169A>C	ENSP00000513105.1:p.Lys57Gln
ENST00000562983.2:n.1072A>C
ENST00000690268.1:c.967A>C	ENSP00000509810.1:p.Lys323Gln
ENST00000355740.7:c.*212A>C	ENSP00000347979.3:n.*212A>C
ENST00000612663.5:c.*288A>C	ENSP00000477997.3:n.*288A>C
ENST00000640140.1:n.1058A>C
ENST00000640250.1:n.385A>C
ENST00000640681.1:n.1007A>C
ENST00000652046.1:c.886A>C MANE Select	ENSP00000498466.1:p.Lys296Gln
ENST00000352159.8:c.*203A>C	ENSP00000345601.4:n.*203A>C
ENST00000355279.2:c.861A>C	ENSP00000347426.2:n.861A>C
ENST00000355740.6:c.886A>C	ENSP00000347979.2:p.Lys296Gln
ENST00000357339.6:c.823A>C	ENSP00000349896.2:p.Lys275Gln
ENST00000479522.5:c.*315A>C	ENSP00000424113.1:n.*315A>C
ENST00000484444.5:c.*327A>C	ENSP00000420975.1:n.*327A>C
ENST00000488877.5:c.*327A>C	ENSP00000425159.1:n.*327A>C
ENST00000492756.5:c.714A>C	ENSP00000422453.1:n.714A>C
ENST00000494410.5:c.*244A>C	ENSP00000423755.1:n.*244A>C
ENST00000612663.4:c.*233A>C	ENSP00000477997.2:n.*233A>C
NM_000043.4:c.886A>C , LRG_134t1:c.886A>C	NP_000034.1:p.Lys296Gln
NM_152871.2:c.823A>C	NP_690610.1:p.Lys275Gln
NM_152872.2:c.*198A>C	NP_690611.1:n.*198A>C
NR_028033.2:n.1060A>C
NR_028034.2:n.922A>C
NR_028035.2:n.985A>C
NR_028036.2:n.1123A>C
XM_006717819.2:c.967A>C	XP_006717882.1:p.Lys323Gln
XM_011539764.1:c.1048A>C	XP_011538066.1:p.Lys350Gln
XM_011539765.1:c.985A>C	XP_011538067.1:p.Lys329Gln
XM_011539766.1:c.967A>C	XP_011538068.1:p.Lys323Gln
XM_011539767.1:c.931A>C	XP_011538069.1:p.Lys311Gln
XR_945732.1:n.954A>C
XR_945733.1:n.891A>C
NM_000043.5:c.886A>C	NP_000034.1:p.Lys296Gln
NM_001320619.1:c.*209A>C	NP_001307548.1:n.*209A>C
NM_152871.3:c.823A>C	NP_690610.1:p.Lys275Gln
NM_152872.3:c.*198A>C	NP_690611.1:n.*198A>C
NR_028033.3:n.1032A>C
NR_028034.3:n.894A>C
NR_028035.3:n.957A>C
NR_028036.3:n.1095A>C
NR_135313.1:n.1012A>C
NR_135314.1:n.1195A>C
NR_135315.1:n.948A>C
XM_006717819.3:c.967A>C	XP_006717882.1:p.Lys323Gln
XM_011539764.2:c.1048A>C	XP_011538066.1:p.Lys350Gln
XM_011539765.2:c.985A>C	XP_011538067.1:p.Lys329Gln
XM_011539766.2:c.967A>C	XP_011538068.1:p.Lys323Gln
XM_011539767.3:c.931A>C	XP_011538069.1:p.Lys311Gln
XR_945732.3:n.954A>C
XR_945733.2:n.891A>C
NM_000043.6:c.886A>C MANE Select	NP_000034.1:p.Lys296Gln
NM_001320619.2:c.*209A>C	NP_001307548.1:n.*209A>C
NM_152871.4:c.823A>C	NP_690610.1:p.Lys275Gln
NM_152872.4:c.*198A>C	NP_690611.1:n.*198A>C
NR_028033.4:n.793A>C
NR_028034.4:n.655A>C
NR_028035.4:n.718A>C
NR_028036.4:n.856A>C
NR_135313.2:n.773A>C
NR_135314.2:n.1052A>C
NR_135315.2:n.805A>C