Canonical Allele Identifier: CA381090035

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990634G>T (hg19) ; chr11:g.64223162G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223162G>T , CM000673.2:g.64223162G>T	GRCh38
NC_000011.9:g.63990634G>T , CM000673.1:g.63990634G>T	GRCh37
NC_000011.8:g.63747210G>T	NCBI36
NG_016360.1:g.21483G>T , LRG_180:g.21483G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1797G>T	ENSP00000279227.5:p.Gln599His
ENST00000540554.2:n.3309G>T
ENST00000541252.2:c.1245G>T	ENSP00000438885.2:p.Gln415His
ENST00000544997.6:c.1785G>T	ENSP00000445778.2:p.Gln595His
ENST00000545896.2:c.349G>T	ENSP00000440209.2:p.Val117Leu
ENST00000546255.2:n.2089G>T
ENST00000698845.1:c.*980G>T	ENSP00000513981.1:n.*980G>T
ENST00000698846.1:n.2031G>T
ENST00000698847.1:c.*1190G>T	ENSP00000513982.1:n.*1190G>T
ENST00000698850.1:n.3806G>T
ENST00000698852.1:c.1785G>T	ENSP00000513984.1:p.Gln595His
ENST00000698853.1:c.*1014G>T	ENSP00000513985.1:n.*1014G>T
ENST00000698854.1:c.*1115G>T	ENSP00000513986.1:n.*1115G>T
ENST00000698855.1:n.3437G>T
ENST00000698856.1:n.3131G>T
ENST00000698859.1:n.2295G>T
ENST00000698860.1:c.1797G>T	ENSP00000513988.1:p.Gln599His
ENST00000698861.1:c.1785G>T	ENSP00000513989.1:p.Gln595His
ENST00000698862.1:c.*1081G>T	ENSP00000513990.1:n.*1081G>T
ENST00000698863.1:c.1785G>T	ENSP00000513991.1:p.Gln595His
ENST00000698864.1:n.2346G>T
ENST00000698865.1:c.1806G>T	ENSP00000513992.1:p.Gln602His
ENST00000698866.1:c.*1573G>T	ENSP00000513993.1:n.*1573G>T
ENST00000698867.1:n.5760G>T
ENST00000698868.1:c.1650G>T	ENSP00000513994.1:p.Gln550His
ENST00000698869.1:c.1551G>T	ENSP00000513995.1:p.Gln517His
ENST00000698870.1:c.1785G>T	ENSP00000513996.1:p.Gln595His
ENST00000698871.1:n.2308G>T
ENST00000698872.1:c.*574G>T	ENSP00000513997.1:n.*574G>T
ENST00000698873.1:c.*980G>T	ENSP00000513998.1:n.*980G>T
ENST00000698874.1:c.1245G>T	ENSP00000513999.1:p.Gln415His
ENST00000698875.1:n.1645G>T
ENST00000698876.1:n.1833G>T
ENST00000698877.1:n.1353G>T
ENST00000698878.1:c.1779G>T	ENSP00000514000.1:p.Gln593His
ENST00000698880.1:c.1653G>T
ENST00000345728.10:c.1785G>T MANE Select	ENSP00000339950.5:p.Gln595His
ENST00000279227.9:c.1797G>T	ENSP00000279227.5:p.Gln599His
ENST00000345728.9:c.1785G>T	ENSP00000339950.5:p.Gln595His
ENST00000545896.1:c.348G>T	ENSP00000440209.1:p.Gln116His
NM_031471.5:c.1785G>T	NP_113659.3:p.Gln595His
NM_178443.2:c.1797G>T , LRG_180t1:c.1797G>T	NP_848537.1:p.Gln599His
XM_011545294.1:c.1797G>T	XP_011543596.1:p.Gln599His
XM_011545295.1:c.1257G>T	XP_011543597.1:p.Gln419His
XM_011545296.1:c.1257G>T	XP_011543598.1:p.Gln419His
XM_011545294.3:c.1797G>T	XP_011543596.1:p.Gln599His
XM_011545295.2:c.1257G>T	XP_011543597.1:p.Gln419His
XM_017018398.2:c.1785G>T	XP_016873887.1:p.Gln595His
XM_017018399.1:c.1245G>T	XP_016873888.1:p.Gln415His
NM_031471.6:c.1785G>T MANE Select	NP_113659.3:p.Gln595His
NM_001382361.1:c.1785G>T	NP_001369290.1:p.Gln595His
NM_001382362.1:c.1797G>T	NP_001369291.1:p.Gln599His
NM_001382363.1:c.1245G>T	NP_001369292.1:p.Gln415His
NM_001382364.1:c.1257G>T	NP_001369293.1:p.Gln419His
NM_001382448.1:c.1785G>T	NP_001369377.1:p.Gln595His
NM_178443.3:c.1797G>T	NP_848537.1:p.Gln599His