Canonical Allele Identifier: CA470975038

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774204C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014447C>G , CM000672.2:g.89014447C>G	GRCh38
NC_000010.10:g.90774204C>G , CM000672.1:g.90774204C>G	GRCh37
NC_000010.9:g.90764184C>G	NCBI36
NG_009089.2:g.28917C>G , LRG_134:g.28917C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1314C>G
ENST00000355740.8:c.*328C>G	ENSP00000347979.3:n.*328C>G
ENST00000357339.7:c.942C>G	ENSP00000349896.2:p.Val314=
ENST00000371857.8:n.2550C>G
ENST00000460510.6:c.288C>G	ENSP00000512812.1:p.Val96=
ENST00000466081.6:n.2654C>G
ENST00000477270.6:c.1050C>G	ENSP00000512813.1:p.Val350=
ENST00000479522.6:c.*434C>G	ENSP00000424113.1:n.*434C>G
ENST00000484444.6:c.*446C>G	ENSP00000420975.1:n.*446C>G
ENST00000488877.6:c.896C>G	ENSP00000425159.1:n.896C>G
ENST00000492756.7:c.*434C>G	ENSP00000422453.1:n.*434C>G
ENST00000494799.6:c.288C>G	ENSP00000512834.1:p.Val96=
ENST00000562983.3:c.288C>G	ENSP00000512845.1:p.Val96=
ENST00000612663.6:c.*407C>G	ENSP00000477997.3:n.*407C>G
ENST00000640140.2:n.1150C>G
ENST00000640250.2:n.504C>G
ENST00000640681.2:n.1109C>G
ENST00000696723.1:n.4638C>G
ENST00000696741.1:n.2643C>G
ENST00000696742.1:n.2370C>G
ENST00000696743.1:n.3773C>G
ENST00000696744.1:n.1044C>G
ENST00000696767.1:n.1339C>G
ENST00000696768.1:c.*328C>G	ENSP00000512859.1:n.*328C>G
ENST00000696769.1:n.2694C>G
ENST00000696771.1:c.288C>G	ENSP00000512860.1:p.Val96=
ENST00000696772.1:n.2608C>G
ENST00000696773.1:n.2347C>G
ENST00000696774.1:n.6115C>G
ENST00000696776.1:c.1098C>G	ENSP00000512861.1:p.Val366=
ENST00000696777.1:n.2413C>G
ENST00000696778.1:n.1441C>G
ENST00000696779.1:c.612C>G	ENSP00000512862.1:p.Val204=
ENST00000696780.1:c.1035C>G	ENSP00000512863.1:p.Val345=
ENST00000696781.1:c.750C>G	ENSP00000512864.1:p.Val250=
ENST00000696782.1:c.*407C>G	ENSP00000512865.1:n.*407C>G
ENST00000696783.1:n.2873C>G
ENST00000696992.1:n.2122C>G
ENST00000696995.1:n.4534C>G
ENST00000696996.1:n.2447C>G
ENST00000696997.1:c.*635C>G	ENSP00000513028.1:n.*635C>G
ENST00000696998.1:n.2259C>G
ENST00000696999.1:c.288C>G	ENSP00000513029.1:p.Val96=
ENST00000697036.1:c.*421C>G	ENSP00000513060.1:n.*421C>G
ENST00000697037.1:n.1040C>G
ENST00000697093.1:n.3241C>G
ENST00000697094.1:n.3588C>G
ENST00000697095.1:c.*2206C>G	ENSP00000513104.1:n.*2206C>G
ENST00000697096.1:n.2138C>G
ENST00000697097.1:c.288C>G	ENSP00000513105.1:p.Val96=
ENST00000562983.2:n.1191C>G
ENST00000690268.1:c.1086C>G	ENSP00000509810.1:p.Val362=
ENST00000355740.7:c.*331C>G	ENSP00000347979.3:n.*331C>G
ENST00000612663.5:c.*407C>G	ENSP00000477997.3:n.*407C>G
ENST00000640140.1:n.1177C>G
ENST00000640250.1:n.504C>G
ENST00000640681.1:n.1126C>G
ENST00000652046.1:c.1005C>G MANE Select	ENSP00000498466.1:p.Val335=
ENST00000352159.8:c.*322C>G	ENSP00000345601.4:n.*322C>G
ENST00000355279.2:c.980C>G	ENSP00000347426.2:n.980C>G
ENST00000355740.6:c.1005C>G	ENSP00000347979.2:p.Val335=
ENST00000357339.6:c.942C>G	ENSP00000349896.2:p.Val314=
ENST00000479522.5:c.*434C>G	ENSP00000424113.1:n.*434C>G
ENST00000484444.5:c.*446C>G	ENSP00000420975.1:n.*446C>G
ENST00000488877.5:c.*446C>G	ENSP00000425159.1:n.*446C>G
ENST00000492756.5:c.833C>G	ENSP00000422453.1:n.833C>G
ENST00000494410.5:c.*363C>G	ENSP00000423755.1:n.*363C>G
ENST00000612663.4:c.*352C>G	ENSP00000477997.2:n.*352C>G
NM_000043.4:c.1005C>G , LRG_134t1:c.1005C>G	NP_000034.1:p.Val335=
NM_152871.2:c.942C>G	NP_690610.1:p.Val314=
NM_152872.2:c.*317C>G	NP_690611.1:n.*317C>G
NR_028033.2:n.1179C>G
NR_028034.2:n.1041C>G
NR_028035.2:n.1104C>G
NR_028036.2:n.1242C>G
XM_006717819.2:c.1086C>G	XP_006717882.1:p.Val362=
XM_011539764.1:c.1167C>G	XP_011538066.1:p.Val389=
XM_011539765.1:c.1104C>G	XP_011538067.1:p.Val368=
XM_011539766.1:c.1086C>G	XP_011538068.1:p.Val362=
XM_011539767.1:c.1050C>G	XP_011538069.1:p.Val350=
XR_945733.1:n.1010C>G
NM_000043.5:c.1005C>G	NP_000034.1:p.Val335=
NM_001320619.1:c.*328C>G	NP_001307548.1:n.*328C>G
NM_152871.3:c.942C>G	NP_690610.1:p.Val314=
NM_152872.3:c.*317C>G	NP_690611.1:n.*317C>G
NR_028033.3:n.1151C>G
NR_028034.3:n.1013C>G
NR_028035.3:n.1076C>G
NR_028036.3:n.1214C>G
NR_135313.1:n.1131C>G
NR_135314.1:n.1314C>G
NR_135315.1:n.1067C>G
XM_006717819.3:c.1086C>G	XP_006717882.1:p.Val362=
XM_011539764.2:c.1167C>G	XP_011538066.1:p.Val389=
XM_011539765.2:c.1104C>G	XP_011538067.1:p.Val368=
XM_011539766.2:c.1086C>G	XP_011538068.1:p.Val362=
XM_011539767.3:c.1050C>G	XP_011538069.1:p.Val350=
XR_945732.3:n.1073C>G
XR_945733.2:n.1010C>G
NM_000043.6:c.1005C>G MANE Select	NP_000034.1:p.Val335=
NM_001320619.2:c.*328C>G	NP_001307548.1:n.*328C>G
NM_152871.4:c.942C>G	NP_690610.1:p.Val314=
NM_152872.4:c.*317C>G	NP_690611.1:n.*317C>G
NR_028033.4:n.912C>G
NR_028034.4:n.774C>G
NR_028035.4:n.837C>G
NR_028036.4:n.975C>G
NR_135313.2:n.892C>G
NR_135314.2:n.1171C>G
NR_135315.2:n.924C>G