Canonical Allele Identifier: CA475151810

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990589C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223117C>A , CM000673.2:g.64223117C>A	GRCh38
NC_000011.9:g.63990589C>A , CM000673.1:g.63990589C>A	GRCh37
NC_000011.8:g.63747165C>A	NCBI36
NG_016360.1:g.21438C>A , LRG_180:g.21438C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1752C>A	ENSP00000279227.5:p.Ala584=
ENST00000540554.2:n.3264C>A
ENST00000541252.2:c.1200C>A	ENSP00000438885.2:p.Ala400=
ENST00000544997.6:c.1740C>A	ENSP00000445778.2:p.Ala580=
ENST00000545896.2:c.304C>A	ENSP00000440209.2:p.Arg102Ser
ENST00000546255.2:n.2044C>A
ENST00000698845.1:c.*935C>A	ENSP00000513981.1:n.*935C>A
ENST00000698846.1:n.1986C>A
ENST00000698847.1:c.*1145C>A	ENSP00000513982.1:n.*1145C>A
ENST00000698850.1:n.3761C>A
ENST00000698852.1:c.1740C>A	ENSP00000513984.1:p.Ala580=
ENST00000698853.1:c.*969C>A	ENSP00000513985.1:n.*969C>A
ENST00000698854.1:c.*1070C>A	ENSP00000513986.1:n.*1070C>A
ENST00000698855.1:n.3392C>A
ENST00000698856.1:n.3086C>A
ENST00000698859.1:n.2250C>A
ENST00000698860.1:c.1752C>A	ENSP00000513988.1:p.Ala584=
ENST00000698861.1:c.1740C>A	ENSP00000513989.1:p.Ala580=
ENST00000698862.1:c.*1036C>A	ENSP00000513990.1:n.*1036C>A
ENST00000698863.1:c.1740C>A	ENSP00000513991.1:p.Ala580=
ENST00000698864.1:n.2301C>A
ENST00000698865.1:c.1761C>A	ENSP00000513992.1:p.Ala587=
ENST00000698866.1:c.*1528C>A	ENSP00000513993.1:n.*1528C>A
ENST00000698867.1:n.5715C>A
ENST00000698868.1:c.1605C>A	ENSP00000513994.1:p.Ala535=
ENST00000698869.1:c.1506C>A	ENSP00000513995.1:p.Ala502=
ENST00000698870.1:c.1740C>A	ENSP00000513996.1:p.Ala580=
ENST00000698871.1:n.2263C>A
ENST00000698872.1:c.*529C>A	ENSP00000513997.1:n.*529C>A
ENST00000698873.1:c.*935C>A	ENSP00000513998.1:n.*935C>A
ENST00000698874.1:c.1200C>A	ENSP00000513999.1:p.Ala400=
ENST00000698875.1:n.1600C>A
ENST00000698876.1:n.1788C>A
ENST00000698877.1:n.1308C>A
ENST00000698878.1:c.1734C>A	ENSP00000514000.1:p.Ala578=
ENST00000698880.1:c.1608C>A
ENST00000345728.10:c.1740C>A MANE Select	ENSP00000339950.5:p.Ala580=
ENST00000279227.9:c.1752C>A	ENSP00000279227.5:p.Ala584=
ENST00000345728.9:c.1740C>A	ENSP00000339950.5:p.Ala580=
ENST00000540554.1:n.376C>A
ENST00000545896.1:c.303C>A	ENSP00000440209.1:p.Ala101=
NM_031471.5:c.1740C>A	NP_113659.3:p.Ala580=
NM_178443.2:c.1752C>A , LRG_180t1:c.1752C>A	NP_848537.1:p.Ala584=
XM_011545294.1:c.1752C>A	XP_011543596.1:p.Ala584=
XM_011545295.1:c.1212C>A	XP_011543597.1:p.Ala404=
XM_011545296.1:c.1212C>A	XP_011543598.1:p.Ala404=
XM_011545294.3:c.1752C>A	XP_011543596.1:p.Ala584=
XM_011545295.2:c.1212C>A	XP_011543597.1:p.Ala404=
XM_017018398.2:c.1740C>A	XP_016873887.1:p.Ala580=
XM_017018399.1:c.1200C>A	XP_016873888.1:p.Ala400=
NM_031471.6:c.1740C>A MANE Select	NP_113659.3:p.Ala580=
NM_001382361.1:c.1740C>A	NP_001369290.1:p.Ala580=
NM_001382362.1:c.1752C>A	NP_001369291.1:p.Ala584=
NM_001382363.1:c.1200C>A	NP_001369292.1:p.Ala400=
NM_001382364.1:c.1212C>A	NP_001369293.1:p.Ala404=
NM_001382448.1:c.1740C>A	NP_001369377.1:p.Ala580=
NM_178443.3:c.1752C>A	NP_848537.1:p.Ala584=