Canonical Allele Identifier: CA381089631

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990558C>A (hg19) ; chr11:g.64223086C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223086C>A , CM000673.2:g.64223086C>A	GRCh38
NC_000011.9:g.63990558C>A , CM000673.1:g.63990558C>A	GRCh37
NC_000011.8:g.63747134C>A	NCBI36
NG_016360.1:g.21407C>A , LRG_180:g.21407C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1721C>A	ENSP00000279227.5:p.Ala574Asp
ENST00000540554.2:n.3233C>A
ENST00000541252.2:c.1169C>A	ENSP00000438885.2:p.Ala390Asp
ENST00000544997.6:c.1709C>A	ENSP00000445778.2:p.Ala570Asp
ENST00000545896.2:c.273C>A	ENSP00000440209.2:p.Arg91=
ENST00000546255.2:n.2013C>A
ENST00000698845.1:c.*904C>A	ENSP00000513981.1:n.*904C>A
ENST00000698846.1:n.1955C>A
ENST00000698847.1:c.*1114C>A	ENSP00000513982.1:n.*1114C>A
ENST00000698850.1:n.3730C>A
ENST00000698852.1:c.1709C>A	ENSP00000513984.1:p.Ala570Asp
ENST00000698853.1:c.*938C>A	ENSP00000513985.1:n.*938C>A
ENST00000698854.1:c.*1039C>A	ENSP00000513986.1:n.*1039C>A
ENST00000698855.1:n.3361C>A
ENST00000698856.1:n.3055C>A
ENST00000698859.1:n.2219C>A
ENST00000698860.1:c.1721C>A	ENSP00000513988.1:p.Ala574Asp
ENST00000698861.1:c.1709C>A	ENSP00000513989.1:p.Ala570Asp
ENST00000698862.1:c.*1005C>A	ENSP00000513990.1:n.*1005C>A
ENST00000698863.1:c.1709C>A	ENSP00000513991.1:p.Ala570Asp
ENST00000698864.1:n.2270C>A
ENST00000698865.1:c.1730C>A	ENSP00000513992.1:p.Ala577Asp
ENST00000698866.1:c.*1497C>A	ENSP00000513993.1:n.*1497C>A
ENST00000698867.1:n.5684C>A
ENST00000698868.1:c.1574C>A	ENSP00000513994.1:p.Ala525Asp
ENST00000698869.1:c.1475C>A	ENSP00000513995.1:p.Ala492Asp
ENST00000698870.1:c.1709C>A	ENSP00000513996.1:p.Ala570Asp
ENST00000698871.1:n.2232C>A
ENST00000698872.1:c.*498C>A	ENSP00000513997.1:n.*498C>A
ENST00000698873.1:c.*904C>A	ENSP00000513998.1:n.*904C>A
ENST00000698874.1:c.1169C>A	ENSP00000513999.1:p.Ala390Asp
ENST00000698875.1:n.1569C>A
ENST00000698876.1:n.1757C>A
ENST00000698877.1:n.1277C>A
ENST00000698878.1:c.1703C>A	ENSP00000514000.1:p.Ala568Asp
ENST00000698880.1:c.1577C>A
ENST00000345728.10:c.1709C>A MANE Select	ENSP00000339950.5:p.Ala570Asp
ENST00000279227.9:c.1721C>A	ENSP00000279227.5:p.Ala574Asp
ENST00000345728.9:c.1709C>A	ENSP00000339950.5:p.Ala570Asp
ENST00000540554.1:n.345C>A
ENST00000545896.1:c.272C>A	ENSP00000440209.1:p.Ala91Asp
NM_031471.5:c.1709C>A	NP_113659.3:p.Ala570Asp
NM_178443.2:c.1721C>A , LRG_180t1:c.1721C>A	NP_848537.1:p.Ala574Asp
XM_011545294.1:c.1721C>A	XP_011543596.1:p.Ala574Asp
XM_011545295.1:c.1181C>A	XP_011543597.1:p.Ala394Asp
XM_011545296.1:c.1181C>A	XP_011543598.1:p.Ala394Asp
XM_011545294.3:c.1721C>A	XP_011543596.1:p.Ala574Asp
XM_011545295.2:c.1181C>A	XP_011543597.1:p.Ala394Asp
XM_017018398.2:c.1709C>A	XP_016873887.1:p.Ala570Asp
XM_017018399.1:c.1169C>A	XP_016873888.1:p.Ala390Asp
NM_031471.6:c.1709C>A MANE Select	NP_113659.3:p.Ala570Asp
NM_001382361.1:c.1709C>A	NP_001369290.1:p.Ala570Asp
NM_001382362.1:c.1721C>A	NP_001369291.1:p.Ala574Asp
NM_001382363.1:c.1169C>A	NP_001369292.1:p.Ala390Asp
NM_001382364.1:c.1181C>A	NP_001369293.1:p.Ala394Asp
NM_001382448.1:c.1709C>A	NP_001369377.1:p.Ala570Asp
NM_178443.3:c.1721C>A	NP_848537.1:p.Ala574Asp