Canonical Allele Identifier: CA381087762

Gene: FERMT3

Linked Data

• dbSNP Id: rs1946656787
• MyVariant Identifiers: chr11:g.63988012C>T (hg19) ; chr11:g.64220540C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220540C>T , CM000673.2:g.64220540C>T	GRCh38
NC_000011.9:g.63988012C>T , CM000673.1:g.63988012C>T	GRCh37
NC_000011.8:g.63744588C>T	NCBI36
NG_016360.1:g.18861C>T , LRG_180:g.18861C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1428C>T	ENSP00000279227.5:p.Phe476=
ENST00000540554.2:n.2594C>T
ENST00000541252.2:c.876C>T	ENSP00000438885.2:p.Phe292=
ENST00000541326.6:n.837C>T
ENST00000544997.6:c.1416C>T	ENSP00000445778.2:p.Phe472=
ENST00000545896.2:c.105C>T	ENSP00000440209.2:p.Phe35=
ENST00000546255.2:n.1720C>T
ENST00000698845.1:c.*611C>T	ENSP00000513981.1:n.*611C>T
ENST00000698846.1:n.1662C>T
ENST00000698847.1:c.*821C>T	ENSP00000513982.1:n.*821C>T
ENST00000698849.1:n.536C>T
ENST00000698850.1:n.1184C>T
ENST00000698852.1:c.1416C>T	ENSP00000513984.1:p.Phe472=
ENST00000698853.1:c.*645C>T	ENSP00000513985.1:n.*645C>T
ENST00000698854.1:c.*746C>T	ENSP00000513986.1:n.*746C>T
ENST00000698855.1:n.3068C>T
ENST00000698856.1:n.2762C>T
ENST00000698859.1:n.1580C>T
ENST00000698860.1:c.1428C>T	ENSP00000513988.1:p.Phe476=
ENST00000698861.1:c.1416C>T	ENSP00000513989.1:p.Phe472=
ENST00000698862.1:c.*712C>T	ENSP00000513990.1:n.*712C>T
ENST00000698863.1:c.1416C>T	ENSP00000513991.1:p.Phe472=
ENST00000698864.1:n.1631C>T
ENST00000698865.1:c.1437C>T	ENSP00000513992.1:p.Phe479=
ENST00000698866.1:c.*930C>T	ENSP00000513993.1:n.*930C>T
ENST00000698867.1:n.5391C>T
ENST00000698868.1:c.1281C>T	ENSP00000513994.1:p.Phe427=
ENST00000698869.1:c.1311+214C>T	ENSP00000513995.1:n.1311+214C>T
ENST00000698870.1:c.1416C>T	ENSP00000513996.1:p.Phe472=
ENST00000698871.1:n.1939C>T
ENST00000698872.1:c.*205C>T	ENSP00000513997.1:n.*205C>T
ENST00000698873.1:c.*611C>T	ENSP00000513998.1:n.*611C>T
ENST00000698874.1:c.876C>T	ENSP00000513999.1:p.Phe292=
ENST00000698875.1:n.1276C>T
ENST00000698876.1:n.1464C>T
ENST00000698877.1:n.984C>T
ENST00000698878.1:c.1410C>T	ENSP00000514000.1:p.Phe470=
ENST00000698880.1:c.1284C>T
ENST00000345728.10:c.1416C>T MANE Select	ENSP00000339950.5:p.Phe472=
ENST00000279227.9:c.1428C>T	ENSP00000279227.5:p.Phe476=
ENST00000345728.9:c.1416C>T	ENSP00000339950.5:p.Phe472=
ENST00000541326.5:n.832C>T
ENST00000545896.1:c.104C>T	ENSP00000440209.1:p.Ser35Phe
NM_031471.5:c.1416C>T	NP_113659.3:p.Phe472=
NM_178443.2:c.1428C>T , LRG_180t1:c.1428C>T	NP_848537.1:p.Phe476=
XM_011545294.1:c.1428C>T	XP_011543596.1:p.Phe476=
XM_011545295.1:c.888C>T	XP_011543597.1:p.Phe296=
XM_011545296.1:c.888C>T	XP_011543598.1:p.Phe296=
XM_011545294.3:c.1428C>T	XP_011543596.1:p.Phe476=
XM_011545295.2:c.888C>T	XP_011543597.1:p.Phe296=
XM_017018398.2:c.1416C>T	XP_016873887.1:p.Phe472=
XM_017018399.1:c.876C>T	XP_016873888.1:p.Phe292=
NM_031471.6:c.1416C>T MANE Select	NP_113659.3:p.Phe472=
NM_001382361.1:c.1416C>T	NP_001369290.1:p.Phe472=
NM_001382362.1:c.1428C>T	NP_001369291.1:p.Phe476=
NM_001382363.1:c.876C>T	NP_001369292.1:p.Phe292=
NM_001382364.1:c.888C>T	NP_001369293.1:p.Phe296=
NM_001382448.1:c.1416C>T	NP_001369377.1:p.Phe472=
NM_178443.3:c.1428C>T	NP_848537.1:p.Phe476=