Canonical Allele Identifier: CA381089851

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990602G>A (hg19) ; chr11:g.64223130G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223130G>A , CM000673.2:g.64223130G>A	GRCh38
NC_000011.9:g.63990602G>A , CM000673.1:g.63990602G>A	GRCh37
NC_000011.8:g.63747178G>A	NCBI36
NG_016360.1:g.21451G>A , LRG_180:g.21451G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1765G>A	ENSP00000279227.5:p.Val589Ile
ENST00000540554.2:n.3277G>A
ENST00000541252.2:c.1213G>A	ENSP00000438885.2:p.Val405Ile
ENST00000544997.6:c.1753G>A	ENSP00000445778.2:p.Val585Ile
ENST00000545896.2:c.317G>A	ENSP00000440209.2:p.Gly106Asp
ENST00000546255.2:n.2057G>A
ENST00000698845.1:c.*948G>A	ENSP00000513981.1:n.*948G>A
ENST00000698846.1:n.1999G>A
ENST00000698847.1:c.*1158G>A	ENSP00000513982.1:n.*1158G>A
ENST00000698850.1:n.3774G>A
ENST00000698852.1:c.1753G>A	ENSP00000513984.1:p.Val585Ile
ENST00000698853.1:c.*982G>A	ENSP00000513985.1:n.*982G>A
ENST00000698854.1:c.*1083G>A	ENSP00000513986.1:n.*1083G>A
ENST00000698855.1:n.3405G>A
ENST00000698856.1:n.3099G>A
ENST00000698859.1:n.2263G>A
ENST00000698860.1:c.1765G>A	ENSP00000513988.1:p.Val589Ile
ENST00000698861.1:c.1753G>A	ENSP00000513989.1:p.Val585Ile
ENST00000698862.1:c.*1049G>A	ENSP00000513990.1:n.*1049G>A
ENST00000698863.1:c.1753G>A	ENSP00000513991.1:p.Val585Ile
ENST00000698864.1:n.2314G>A
ENST00000698865.1:c.1774G>A	ENSP00000513992.1:p.Val592Ile
ENST00000698866.1:c.*1541G>A	ENSP00000513993.1:n.*1541G>A
ENST00000698867.1:n.5728G>A
ENST00000698868.1:c.1618G>A	ENSP00000513994.1:p.Val540Ile
ENST00000698869.1:c.1519G>A	ENSP00000513995.1:p.Val507Ile
ENST00000698870.1:c.1753G>A	ENSP00000513996.1:p.Val585Ile
ENST00000698871.1:n.2276G>A
ENST00000698872.1:c.*542G>A	ENSP00000513997.1:n.*542G>A
ENST00000698873.1:c.*948G>A	ENSP00000513998.1:n.*948G>A
ENST00000698874.1:c.1213G>A	ENSP00000513999.1:p.Val405Ile
ENST00000698875.1:n.1613G>A
ENST00000698876.1:n.1801G>A
ENST00000698877.1:n.1321G>A
ENST00000698878.1:c.1747G>A	ENSP00000514000.1:p.Val583Ile
ENST00000698880.1:c.1621G>A
ENST00000345728.10:c.1753G>A MANE Select	ENSP00000339950.5:p.Val585Ile
ENST00000279227.9:c.1765G>A	ENSP00000279227.5:p.Val589Ile
ENST00000345728.9:c.1753G>A	ENSP00000339950.5:p.Val585Ile
ENST00000545896.1:c.316G>A	ENSP00000440209.1:p.Val106Ile
NM_031471.5:c.1753G>A	NP_113659.3:p.Val585Ile
NM_178443.2:c.1765G>A , LRG_180t1:c.1765G>A	NP_848537.1:p.Val589Ile
XM_011545294.1:c.1765G>A	XP_011543596.1:p.Val589Ile
XM_011545295.1:c.1225G>A	XP_011543597.1:p.Val409Ile
XM_011545296.1:c.1225G>A	XP_011543598.1:p.Val409Ile
XM_011545294.3:c.1765G>A	XP_011543596.1:p.Val589Ile
XM_011545295.2:c.1225G>A	XP_011543597.1:p.Val409Ile
XM_017018398.2:c.1753G>A	XP_016873887.1:p.Val585Ile
XM_017018399.1:c.1213G>A	XP_016873888.1:p.Val405Ile
NM_031471.6:c.1753G>A MANE Select	NP_113659.3:p.Val585Ile
NM_001382361.1:c.1753G>A	NP_001369290.1:p.Val585Ile
NM_001382362.1:c.1765G>A	NP_001369291.1:p.Val589Ile
NM_001382363.1:c.1213G>A	NP_001369292.1:p.Val405Ile
NM_001382364.1:c.1225G>A	NP_001369293.1:p.Val409Ile
NM_001382448.1:c.1753G>A	NP_001369377.1:p.Val585Ile
NM_178443.3:c.1765G>A	NP_848537.1:p.Val589Ile