Canonical Allele Identifier: CA381087394

Gene: FERMT3

Linked Data

• gnomAD v4: 11-64220452-G-T
• MyVariant Identifiers: chr11:g.63987924G>T (hg19) ; chr11:g.64220452G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220452G>T , CM000673.2:g.64220452G>T	GRCh38
NC_000011.9:g.63987924G>T , CM000673.1:g.63987924G>T	GRCh37
NC_000011.8:g.63744500G>T	NCBI36
NG_016360.1:g.18773G>T , LRG_180:g.18773G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1340G>T	ENSP00000279227.5:p.Arg447Leu
ENST00000540554.2:n.2506G>T
ENST00000541252.2:c.788G>T	ENSP00000438885.2:p.Arg263Leu
ENST00000541326.6:n.749G>T
ENST00000544997.6:c.1328G>T	ENSP00000445778.2:p.Arg443Leu
ENST00000545896.2:c.17G>T	ENSP00000440209.2:p.Arg6Leu
ENST00000546255.2:n.1632G>T
ENST00000698845.1:c.*523G>T	ENSP00000513981.1:n.*523G>T
ENST00000698846.1:n.1574G>T
ENST00000698847.1:c.*733G>T	ENSP00000513982.1:n.*733G>T
ENST00000698848.1:n.626G>T
ENST00000698849.1:n.448G>T
ENST00000698850.1:n.1096G>T
ENST00000698852.1:c.1328G>T	ENSP00000513984.1:p.Arg443Leu
ENST00000698853.1:c.*557G>T	ENSP00000513985.1:n.*557G>T
ENST00000698854.1:c.*658G>T	ENSP00000513986.1:n.*658G>T
ENST00000698855.1:n.2980G>T
ENST00000698856.1:n.2674G>T
ENST00000698859.1:n.1492G>T
ENST00000698860.1:c.1340G>T	ENSP00000513988.1:p.Arg447Leu
ENST00000698861.1:c.1328G>T	ENSP00000513989.1:p.Arg443Leu
ENST00000698862.1:c.*624G>T	ENSP00000513990.1:n.*624G>T
ENST00000698863.1:c.1328G>T	ENSP00000513991.1:p.Arg443Leu
ENST00000698864.1:n.1543G>T
ENST00000698865.1:c.1349G>T	ENSP00000513992.1:p.Arg450Leu
ENST00000698866.1:c.*842G>T	ENSP00000513993.1:n.*842G>T
ENST00000698867.1:n.5303G>T
ENST00000698868.1:c.1193G>T	ENSP00000513994.1:p.Arg398Leu
ENST00000698869.1:c.1311+126G>T	ENSP00000513995.1:n.1311+126G>T
ENST00000698870.1:c.1328G>T	ENSP00000513996.1:p.Arg443Leu
ENST00000698871.1:n.1851G>T
ENST00000698872.1:c.*117G>T	ENSP00000513997.1:n.*117G>T
ENST00000698873.1:c.*523G>T	ENSP00000513998.1:n.*523G>T
ENST00000698874.1:c.788G>T	ENSP00000513999.1:p.Arg263Leu
ENST00000698875.1:n.1188G>T
ENST00000698876.1:n.1376G>T
ENST00000698877.1:n.896G>T
ENST00000698878.1:c.1322G>T	ENSP00000514000.1:p.Arg441Leu
ENST00000698880.1:c.1196G>T
ENST00000345728.10:c.1328G>T MANE Select	ENSP00000339950.5:p.Arg443Leu
ENST00000279227.9:c.1340G>T	ENSP00000279227.5:p.Arg447Leu
ENST00000345728.9:c.1328G>T	ENSP00000339950.5:p.Arg443Leu
ENST00000541326.5:n.744G>T
ENST00000545896.1:c.16G>T	ENSP00000440209.1:p.Ala6Ser
NM_031471.5:c.1328G>T	NP_113659.3:p.Arg443Leu
NM_178443.2:c.1340G>T , LRG_180t1:c.1340G>T	NP_848537.1:p.Arg447Leu
XM_011545294.1:c.1340G>T	XP_011543596.1:p.Arg447Leu
XM_011545295.1:c.800G>T	XP_011543597.1:p.Arg267Leu
XM_011545296.1:c.800G>T	XP_011543598.1:p.Arg267Leu
XM_011545294.3:c.1340G>T	XP_011543596.1:p.Arg447Leu
XM_011545295.2:c.800G>T	XP_011543597.1:p.Arg267Leu
XM_017018398.2:c.1328G>T	XP_016873887.1:p.Arg443Leu
XM_017018399.1:c.788G>T	XP_016873888.1:p.Arg263Leu
NM_031471.6:c.1328G>T MANE Select	NP_113659.3:p.Arg443Leu
NM_001382361.1:c.1328G>T	NP_001369290.1:p.Arg443Leu
NM_001382362.1:c.1340G>T	NP_001369291.1:p.Arg447Leu
NM_001382363.1:c.788G>T	NP_001369292.1:p.Arg263Leu
NM_001382364.1:c.800G>T	NP_001369293.1:p.Arg267Leu
NM_001382448.1:c.1328G>T	NP_001369377.1:p.Arg443Leu
NM_178443.3:c.1340G>T	NP_848537.1:p.Arg447Leu