Canonical Allele Identifier: CA381087767

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63988013C>T (hg19) ; chr11:g.64220541C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220541C>T , CM000673.2:g.64220541C>T	GRCh38
NC_000011.9:g.63988013C>T , CM000673.1:g.63988013C>T	GRCh37
NC_000011.8:g.63744589C>T	NCBI36
NG_016360.1:g.18862C>T , LRG_180:g.18862C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1429C>T	ENSP00000279227.5:p.Leu477Phe
ENST00000540554.2:n.2595C>T
ENST00000541252.2:c.877C>T	ENSP00000438885.2:p.Leu293Phe
ENST00000541326.6:n.838C>T
ENST00000544997.6:c.1417C>T	ENSP00000445778.2:p.Leu473Phe
ENST00000545896.2:c.106C>T	ENSP00000440209.2:p.Leu36Phe
ENST00000546255.2:n.1721C>T
ENST00000698845.1:c.*612C>T	ENSP00000513981.1:n.*612C>T
ENST00000698846.1:n.1663C>T
ENST00000698847.1:c.*822C>T	ENSP00000513982.1:n.*822C>T
ENST00000698849.1:n.537C>T
ENST00000698850.1:n.1185C>T
ENST00000698852.1:c.1417C>T	ENSP00000513984.1:p.Leu473Phe
ENST00000698853.1:c.*646C>T	ENSP00000513985.1:n.*646C>T
ENST00000698854.1:c.*747C>T	ENSP00000513986.1:n.*747C>T
ENST00000698855.1:n.3069C>T
ENST00000698856.1:n.2763C>T
ENST00000698859.1:n.1581C>T
ENST00000698860.1:c.1429C>T	ENSP00000513988.1:p.Leu477Phe
ENST00000698861.1:c.1417C>T	ENSP00000513989.1:p.Leu473Phe
ENST00000698862.1:c.*713C>T	ENSP00000513990.1:n.*713C>T
ENST00000698863.1:c.1417C>T	ENSP00000513991.1:p.Leu473Phe
ENST00000698864.1:n.1632C>T
ENST00000698865.1:c.1438C>T	ENSP00000513992.1:p.Leu480Phe
ENST00000698866.1:c.*931C>T	ENSP00000513993.1:n.*931C>T
ENST00000698867.1:n.5392C>T
ENST00000698868.1:c.1282C>T	ENSP00000513994.1:p.Leu428Phe
ENST00000698869.1:c.1311+215C>T	ENSP00000513995.1:n.1311+215C>T
ENST00000698870.1:c.1417C>T	ENSP00000513996.1:p.Leu473Phe
ENST00000698871.1:n.1940C>T
ENST00000698872.1:c.*206C>T	ENSP00000513997.1:n.*206C>T
ENST00000698873.1:c.*612C>T	ENSP00000513998.1:n.*612C>T
ENST00000698874.1:c.877C>T	ENSP00000513999.1:p.Leu293Phe
ENST00000698875.1:n.1277C>T
ENST00000698876.1:n.1465C>T
ENST00000698877.1:n.985C>T
ENST00000698878.1:c.1411C>T	ENSP00000514000.1:p.Leu471Phe
ENST00000698880.1:c.1285C>T
ENST00000345728.10:c.1417C>T MANE Select	ENSP00000339950.5:p.Leu473Phe
ENST00000279227.9:c.1429C>T	ENSP00000279227.5:p.Leu477Phe
ENST00000345728.9:c.1417C>T	ENSP00000339950.5:p.Leu473Phe
ENST00000541326.5:n.833C>T
ENST00000545896.1:c.105C>T	ENSP00000440209.1:p.Ser35=
NM_031471.5:c.1417C>T	NP_113659.3:p.Leu473Phe
NM_178443.2:c.1429C>T , LRG_180t1:c.1429C>T	NP_848537.1:p.Leu477Phe
XM_011545294.1:c.1429C>T	XP_011543596.1:p.Leu477Phe
XM_011545295.1:c.889C>T	XP_011543597.1:p.Leu297Phe
XM_011545296.1:c.889C>T	XP_011543598.1:p.Leu297Phe
XM_011545294.3:c.1429C>T	XP_011543596.1:p.Leu477Phe
XM_011545295.2:c.889C>T	XP_011543597.1:p.Leu297Phe
XM_017018398.2:c.1417C>T	XP_016873887.1:p.Leu473Phe
XM_017018399.1:c.877C>T	XP_016873888.1:p.Leu293Phe
NM_031471.6:c.1417C>T MANE Select	NP_113659.3:p.Leu473Phe
NM_001382361.1:c.1417C>T	NP_001369290.1:p.Leu473Phe
NM_001382362.1:c.1429C>T	NP_001369291.1:p.Leu477Phe
NM_001382363.1:c.877C>T	NP_001369292.1:p.Leu293Phe
NM_001382364.1:c.889C>T	NP_001369293.1:p.Leu297Phe
NM_001382448.1:c.1417C>T	NP_001369377.1:p.Leu473Phe
NM_178443.3:c.1429C>T	NP_848537.1:p.Leu477Phe