Canonical Allele Identifier: CA381089901

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990614C>A (hg19) ; chr11:g.64223142C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223142C>A , CM000673.2:g.64223142C>A	GRCh38
NC_000011.9:g.63990614C>A , CM000673.1:g.63990614C>A	GRCh37
NC_000011.8:g.63747190C>A	NCBI36
NG_016360.1:g.21463C>A , LRG_180:g.21463C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1777C>A	ENSP00000279227.5:p.Arg593Ser
ENST00000540554.2:n.3289C>A
ENST00000541252.2:c.1225C>A	ENSP00000438885.2:p.Arg409Ser
ENST00000544997.6:c.1765C>A	ENSP00000445778.2:p.Arg589Ser
ENST00000545896.2:c.329C>A	ENSP00000440209.2:p.Ala110Glu
ENST00000546255.2:n.2069C>A
ENST00000698845.1:c.*960C>A	ENSP00000513981.1:n.*960C>A
ENST00000698846.1:n.2011C>A
ENST00000698847.1:c.*1170C>A	ENSP00000513982.1:n.*1170C>A
ENST00000698850.1:n.3786C>A
ENST00000698852.1:c.1765C>A	ENSP00000513984.1:p.Arg589Ser
ENST00000698853.1:c.*994C>A	ENSP00000513985.1:n.*994C>A
ENST00000698854.1:c.*1095C>A	ENSP00000513986.1:n.*1095C>A
ENST00000698855.1:n.3417C>A
ENST00000698856.1:n.3111C>A
ENST00000698859.1:n.2275C>A
ENST00000698860.1:c.1777C>A	ENSP00000513988.1:p.Arg593Ser
ENST00000698861.1:c.1765C>A	ENSP00000513989.1:p.Arg589Ser
ENST00000698862.1:c.*1061C>A	ENSP00000513990.1:n.*1061C>A
ENST00000698863.1:c.1765C>A	ENSP00000513991.1:p.Arg589Ser
ENST00000698864.1:n.2326C>A
ENST00000698865.1:c.1786C>A	ENSP00000513992.1:p.Arg596Ser
ENST00000698866.1:c.*1553C>A	ENSP00000513993.1:n.*1553C>A
ENST00000698867.1:n.5740C>A
ENST00000698868.1:c.1630C>A	ENSP00000513994.1:p.Arg544Ser
ENST00000698869.1:c.1531C>A	ENSP00000513995.1:p.Arg511Ser
ENST00000698870.1:c.1765C>A	ENSP00000513996.1:p.Arg589Ser
ENST00000698871.1:n.2288C>A
ENST00000698872.1:c.*554C>A	ENSP00000513997.1:n.*554C>A
ENST00000698873.1:c.*960C>A	ENSP00000513998.1:n.*960C>A
ENST00000698874.1:c.1225C>A	ENSP00000513999.1:p.Arg409Ser
ENST00000698875.1:n.1625C>A
ENST00000698876.1:n.1813C>A
ENST00000698877.1:n.1333C>A
ENST00000698878.1:c.1759C>A	ENSP00000514000.1:p.Arg587Ser
ENST00000698880.1:c.1633C>A
ENST00000345728.10:c.1765C>A MANE Select	ENSP00000339950.5:p.Arg589Ser
ENST00000279227.9:c.1777C>A	ENSP00000279227.5:p.Arg593Ser
ENST00000345728.9:c.1765C>A	ENSP00000339950.5:p.Arg589Ser
ENST00000545896.1:c.328C>A	ENSP00000440209.1:p.Arg110Ser
NM_031471.5:c.1765C>A	NP_113659.3:p.Arg589Ser
NM_178443.2:c.1777C>A , LRG_180t1:c.1777C>A	NP_848537.1:p.Arg593Ser
XM_011545294.1:c.1777C>A	XP_011543596.1:p.Arg593Ser
XM_011545295.1:c.1237C>A	XP_011543597.1:p.Arg413Ser
XM_011545296.1:c.1237C>A	XP_011543598.1:p.Arg413Ser
XM_011545294.3:c.1777C>A	XP_011543596.1:p.Arg593Ser
XM_011545295.2:c.1237C>A	XP_011543597.1:p.Arg413Ser
XM_017018398.2:c.1765C>A	XP_016873887.1:p.Arg589Ser
XM_017018399.1:c.1225C>A	XP_016873888.1:p.Arg409Ser
NM_031471.6:c.1765C>A MANE Select	NP_113659.3:p.Arg589Ser
NM_001382361.1:c.1765C>A	NP_001369290.1:p.Arg589Ser
NM_001382362.1:c.1777C>A	NP_001369291.1:p.Arg593Ser
NM_001382363.1:c.1225C>A	NP_001369292.1:p.Arg409Ser
NM_001382364.1:c.1237C>A	NP_001369293.1:p.Arg413Ser
NM_001382448.1:c.1765C>A	NP_001369377.1:p.Arg589Ser
NM_178443.3:c.1777C>A	NP_848537.1:p.Arg593Ser