Canonical Allele Identifier: CA6069188

Gene: FERMT3

Linked Data

• ClinVar Variation Id: 1400039
• ClinVar RCV Id: RCV001917986
• dbSNP Id: rs184091587
• ExAC: 11:63988112 C / T
• gnomAD v2: 11-63988112-C-T
• gnomAD v3: 11-64220640-C-T
• gnomAD v4: 11-64220640-C-T
• MyVariant Identifiers: chr11:g.63988112C>T (hg19) ; chr11:g.64220640C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220640C>T , CM000673.2:g.64220640C>T	GRCh38
NC_000011.9:g.63988112C>T , CM000673.1:g.63988112C>T	GRCh37
NC_000011.8:g.63744688C>T	NCBI36
NG_016360.1:g.18961C>T , LRG_180:g.18961C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1528C>T	ENSP00000279227.5:p.Arg510Cys
ENST00000540554.2:n.2694C>T
ENST00000541252.2:c.976C>T	ENSP00000438885.2:p.Arg326Cys
ENST00000541326.6:n.937C>T
ENST00000544997.6:c.1516C>T	ENSP00000445778.2:p.Arg506Cys
ENST00000545896.2:c.205C>T	ENSP00000440209.2:p.Arg69Cys
ENST00000546255.2:n.1820C>T
ENST00000698845.1:c.*711C>T	ENSP00000513981.1:n.*711C>T
ENST00000698846.1:n.1762C>T
ENST00000698847.1:c.*921C>T	ENSP00000513982.1:n.*921C>T
ENST00000698849.1:n.636C>T
ENST00000698850.1:n.1284C>T
ENST00000698852.1:c.1516C>T	ENSP00000513984.1:p.Arg506Cys
ENST00000698853.1:c.*745C>T	ENSP00000513985.1:n.*745C>T
ENST00000698854.1:c.*846C>T	ENSP00000513986.1:n.*846C>T
ENST00000698855.1:n.3168C>T
ENST00000698856.1:n.2862C>T
ENST00000698859.1:n.1680C>T
ENST00000698860.1:c.1528C>T	ENSP00000513988.1:p.Arg510Cys
ENST00000698861.1:c.1516C>T	ENSP00000513989.1:p.Arg506Cys
ENST00000698862.1:c.*812C>T	ENSP00000513990.1:n.*812C>T
ENST00000698863.1:c.1516C>T	ENSP00000513991.1:p.Arg506Cys
ENST00000698864.1:n.1731C>T
ENST00000698865.1:c.1537C>T	ENSP00000513992.1:p.Arg513Cys
ENST00000698866.1:c.*1030C>T	ENSP00000513993.1:n.*1030C>T
ENST00000698867.1:n.5491C>T
ENST00000698868.1:c.1381C>T	ENSP00000513994.1:p.Arg461Cys
ENST00000698869.1:c.1311+314C>T	ENSP00000513995.1:n.1311+314C>T
ENST00000698870.1:c.1516C>T	ENSP00000513996.1:p.Arg506Cys
ENST00000698871.1:n.2039C>T
ENST00000698872.1:c.*305C>T	ENSP00000513997.1:n.*305C>T
ENST00000698873.1:c.*711C>T	ENSP00000513998.1:n.*711C>T
ENST00000698874.1:c.976C>T	ENSP00000513999.1:p.Arg326Cys
ENST00000698875.1:n.1376C>T
ENST00000698876.1:n.1564C>T
ENST00000698877.1:n.1084C>T
ENST00000698878.1:c.1510C>T	ENSP00000514000.1:p.Arg504Cys
ENST00000698880.1:c.1384C>T
ENST00000345728.10:c.1516C>T MANE Select	ENSP00000339950.5:p.Arg506Cys
ENST00000279227.9:c.1528C>T	ENSP00000279227.5:p.Arg510Cys
ENST00000345728.9:c.1516C>T	ENSP00000339950.5:p.Arg506Cys
ENST00000545896.1:c.204C>T	ENSP00000440209.1:p.Pro68=
NM_031471.5:c.1516C>T	NP_113659.3:p.Arg506Cys
NM_178443.2:c.1528C>T , LRG_180t1:c.1528C>T	NP_848537.1:p.Arg510Cys
XM_011545294.1:c.1528C>T	XP_011543596.1:p.Arg510Cys
XM_011545295.1:c.988C>T	XP_011543597.1:p.Arg330Cys
XM_011545296.1:c.988C>T	XP_011543598.1:p.Arg330Cys
XM_011545294.3:c.1528C>T	XP_011543596.1:p.Arg510Cys
XM_011545295.2:c.988C>T	XP_011543597.1:p.Arg330Cys
XM_017018398.2:c.1516C>T	XP_016873887.1:p.Arg506Cys
XM_017018399.1:c.976C>T	XP_016873888.1:p.Arg326Cys
NM_031471.6:c.1516C>T MANE Select	NP_113659.3:p.Arg506Cys
NM_001382361.1:c.1516C>T	NP_001369290.1:p.Arg506Cys
NM_001382362.1:c.1528C>T	NP_001369291.1:p.Arg510Cys
NM_001382363.1:c.976C>T	NP_001369292.1:p.Arg326Cys
NM_001382364.1:c.988C>T	NP_001369293.1:p.Arg330Cys
NM_001382448.1:c.1516C>T	NP_001369377.1:p.Arg506Cys
NM_178443.3:c.1528C>T	NP_848537.1:p.Arg510Cys