Canonical Allele Identifier: CA377509980

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774060G>T (hg19) ; chr10:g.89014303G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014303G>T , CM000672.2:g.89014303G>T	GRCh38
NC_000010.10:g.90774060G>T , CM000672.1:g.90774060G>T	GRCh37
NC_000010.9:g.90764040G>T	NCBI36
NG_009089.2:g.28773G>T , LRG_134:g.28773G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1170G>T
ENST00000355740.8:c.*184G>T	ENSP00000347979.3:n.*184G>T
ENST00000357339.7:c.798G>T	ENSP00000349896.2:p.Lys266Asn
ENST00000371857.8:n.2406G>T
ENST00000460510.6:c.144G>T	ENSP00000512812.1:p.Lys48Asn
ENST00000466081.6:n.2510G>T
ENST00000477270.6:c.906G>T	ENSP00000512813.1:p.Lys302Asn
ENST00000479522.6:c.*290G>T	ENSP00000424113.1:n.*290G>T
ENST00000484444.6:c.*302G>T	ENSP00000420975.1:n.*302G>T
ENST00000488877.6:c.752G>T	ENSP00000425159.1:n.752G>T
ENST00000492756.7:c.*290G>T	ENSP00000422453.1:n.*290G>T
ENST00000494799.6:c.144G>T	ENSP00000512834.1:p.Lys48Asn
ENST00000562983.3:c.144G>T	ENSP00000512845.1:p.Lys48Asn
ENST00000612663.6:c.*263G>T	ENSP00000477997.3:n.*263G>T
ENST00000640140.2:n.1006G>T
ENST00000640250.2:n.360G>T
ENST00000640681.2:n.965G>T
ENST00000696723.1:n.4494G>T
ENST00000696741.1:n.2499G>T
ENST00000696742.1:n.2226G>T
ENST00000696743.1:n.3629G>T
ENST00000696744.1:n.900G>T
ENST00000696767.1:n.1195G>T
ENST00000696768.1:c.*184G>T	ENSP00000512859.1:n.*184G>T
ENST00000696769.1:n.2550G>T
ENST00000696771.1:c.144G>T	ENSP00000512860.1:p.Lys48Asn
ENST00000696772.1:n.2464G>T
ENST00000696773.1:n.2203G>T
ENST00000696774.1:n.5971G>T
ENST00000696776.1:c.954G>T	ENSP00000512861.1:p.Lys318Asn
ENST00000696777.1:n.2269G>T
ENST00000696778.1:n.1297G>T
ENST00000696779.1:c.468G>T	ENSP00000512862.1:p.Lys156Asn
ENST00000696780.1:c.891G>T	ENSP00000512863.1:p.Lys297Asn
ENST00000696781.1:c.606G>T	ENSP00000512864.1:p.Lys202Asn
ENST00000696782.1:c.*263G>T	ENSP00000512865.1:n.*263G>T
ENST00000696783.1:n.2729G>T
ENST00000696992.1:n.1978G>T
ENST00000696995.1:n.4390G>T
ENST00000696996.1:n.2303G>T
ENST00000696997.1:c.*491G>T	ENSP00000513028.1:n.*491G>T
ENST00000696998.1:n.2115G>T
ENST00000696999.1:c.144G>T	ENSP00000513029.1:p.Lys48Asn
ENST00000697036.1:c.*277G>T	ENSP00000513060.1:n.*277G>T
ENST00000697037.1:n.896G>T
ENST00000697093.1:n.3097G>T
ENST00000697094.1:n.3444G>T
ENST00000697095.1:c.*2062G>T	ENSP00000513104.1:n.*2062G>T
ENST00000697096.1:n.1994G>T
ENST00000697097.1:c.144G>T	ENSP00000513105.1:p.Lys48Asn
ENST00000562983.2:n.1047G>T
ENST00000690268.1:c.942G>T	ENSP00000509810.1:p.Lys314Asn
ENST00000355740.7:c.*187G>T	ENSP00000347979.3:n.*187G>T
ENST00000612663.5:c.*263G>T	ENSP00000477997.3:n.*263G>T
ENST00000640140.1:n.1033G>T
ENST00000640250.1:n.360G>T
ENST00000640681.1:n.982G>T
ENST00000652046.1:c.861G>T MANE Select	ENSP00000498466.1:p.Lys287Asn
ENST00000352159.8:c.*178G>T	ENSP00000345601.4:n.*178G>T
ENST00000355279.2:c.836G>T	ENSP00000347426.2:n.836G>T
ENST00000355740.6:c.861G>T	ENSP00000347979.2:p.Lys287Asn
ENST00000357339.6:c.798G>T	ENSP00000349896.2:p.Lys266Asn
ENST00000479522.5:c.*290G>T	ENSP00000424113.1:n.*290G>T
ENST00000484444.5:c.*302G>T	ENSP00000420975.1:n.*302G>T
ENST00000488877.5:c.*302G>T	ENSP00000425159.1:n.*302G>T
ENST00000492756.5:c.689G>T	ENSP00000422453.1:n.689G>T
ENST00000494410.5:c.*219G>T	ENSP00000423755.1:n.*219G>T
ENST00000612663.4:c.*208G>T	ENSP00000477997.2:n.*208G>T
NM_000043.4:c.861G>T , LRG_134t1:c.861G>T	NP_000034.1:p.Lys287Asn
NM_152871.2:c.798G>T	NP_690610.1:p.Lys266Asn
NM_152872.2:c.*173G>T	NP_690611.1:n.*173G>T
NR_028033.2:n.1035G>T
NR_028034.2:n.897G>T
NR_028035.2:n.960G>T
NR_028036.2:n.1098G>T
XM_006717819.2:c.942G>T	XP_006717882.1:p.Lys314Asn
XM_011539764.1:c.1023G>T	XP_011538066.1:p.Lys341Asn
XM_011539765.1:c.960G>T	XP_011538067.1:p.Lys320Asn
XM_011539766.1:c.942G>T	XP_011538068.1:p.Lys314Asn
XM_011539767.1:c.906G>T	XP_011538069.1:p.Lys302Asn
XR_945732.1:n.929G>T
XR_945733.1:n.866G>T
NM_000043.5:c.861G>T	NP_000034.1:p.Lys287Asn
NM_001320619.1:c.*184G>T	NP_001307548.1:n.*184G>T
NM_152871.3:c.798G>T	NP_690610.1:p.Lys266Asn
NM_152872.3:c.*173G>T	NP_690611.1:n.*173G>T
NR_028033.3:n.1007G>T
NR_028034.3:n.869G>T
NR_028035.3:n.932G>T
NR_028036.3:n.1070G>T
NR_135313.1:n.987G>T
NR_135314.1:n.1170G>T
NR_135315.1:n.923G>T
XM_006717819.3:c.942G>T	XP_006717882.1:p.Lys314Asn
XM_011539764.2:c.1023G>T	XP_011538066.1:p.Lys341Asn
XM_011539765.2:c.960G>T	XP_011538067.1:p.Lys320Asn
XM_011539766.2:c.942G>T	XP_011538068.1:p.Lys314Asn
XM_011539767.3:c.906G>T	XP_011538069.1:p.Lys302Asn
XR_945732.3:n.929G>T
XR_945733.2:n.866G>T
NM_000043.6:c.861G>T MANE Select	NP_000034.1:p.Lys287Asn
NM_001320619.2:c.*184G>T	NP_001307548.1:n.*184G>T
NM_152871.4:c.798G>T	NP_690610.1:p.Lys266Asn
NM_152872.4:c.*173G>T	NP_690611.1:n.*173G>T
NR_028033.4:n.768G>T
NR_028034.4:n.630G>T
NR_028035.4:n.693G>T
NR_028036.4:n.831G>T
NR_135313.2:n.748G>T
NR_135314.2:n.1027G>T
NR_135315.2:n.780G>T