Canonical Allele Identifier: CA381087992

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63988059A>T (hg19) ; chr11:g.64220587A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220587A>T , CM000673.2:g.64220587A>T	GRCh38
NC_000011.9:g.63988059A>T , CM000673.1:g.63988059A>T	GRCh37
NC_000011.8:g.63744635A>T	NCBI36
NG_016360.1:g.18908A>T , LRG_180:g.18908A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1475A>T	ENSP00000279227.5:p.His492Leu
ENST00000540554.2:n.2641A>T
ENST00000541252.2:c.923A>T	ENSP00000438885.2:p.His308Leu
ENST00000541326.6:n.884A>T
ENST00000544997.6:c.1463A>T	ENSP00000445778.2:p.His488Leu
ENST00000545896.2:c.152A>T	ENSP00000440209.2:p.His51Leu
ENST00000546255.2:n.1767A>T
ENST00000698845.1:c.*658A>T	ENSP00000513981.1:n.*658A>T
ENST00000698846.1:n.1709A>T
ENST00000698847.1:c.*868A>T	ENSP00000513982.1:n.*868A>T
ENST00000698849.1:n.583A>T
ENST00000698850.1:n.1231A>T
ENST00000698852.1:c.1463A>T	ENSP00000513984.1:p.His488Leu
ENST00000698853.1:c.*692A>T	ENSP00000513985.1:n.*692A>T
ENST00000698854.1:c.*793A>T	ENSP00000513986.1:n.*793A>T
ENST00000698855.1:n.3115A>T
ENST00000698856.1:n.2809A>T
ENST00000698859.1:n.1627A>T
ENST00000698860.1:c.1475A>T	ENSP00000513988.1:p.His492Leu
ENST00000698861.1:c.1463A>T	ENSP00000513989.1:p.His488Leu
ENST00000698862.1:c.*759A>T	ENSP00000513990.1:n.*759A>T
ENST00000698863.1:c.1463A>T	ENSP00000513991.1:p.His488Leu
ENST00000698864.1:n.1678A>T
ENST00000698865.1:c.1484A>T	ENSP00000513992.1:p.His495Leu
ENST00000698866.1:c.*977A>T	ENSP00000513993.1:n.*977A>T
ENST00000698867.1:n.5438A>T
ENST00000698868.1:c.1328A>T	ENSP00000513994.1:p.His443Leu
ENST00000698869.1:c.1311+261A>T	ENSP00000513995.1:n.1311+261A>T
ENST00000698870.1:c.1463A>T	ENSP00000513996.1:p.His488Leu
ENST00000698871.1:n.1986A>T
ENST00000698872.1:c.*252A>T	ENSP00000513997.1:n.*252A>T
ENST00000698873.1:c.*658A>T	ENSP00000513998.1:n.*658A>T
ENST00000698874.1:c.923A>T	ENSP00000513999.1:p.His308Leu
ENST00000698875.1:n.1323A>T
ENST00000698876.1:n.1511A>T
ENST00000698877.1:n.1031A>T
ENST00000698878.1:c.1457A>T	ENSP00000514000.1:p.His486Leu
ENST00000698880.1:c.1331A>T
ENST00000345728.10:c.1463A>T MANE Select	ENSP00000339950.5:p.His488Leu
ENST00000279227.9:c.1475A>T	ENSP00000279227.5:p.His492Leu
ENST00000345728.9:c.1463A>T	ENSP00000339950.5:p.His488Leu
ENST00000541326.5:n.879A>T
ENST00000545896.1:c.151A>T	ENSP00000440209.1:p.Thr51Ser
NM_031471.5:c.1463A>T	NP_113659.3:p.His488Leu
NM_178443.2:c.1475A>T , LRG_180t1:c.1475A>T	NP_848537.1:p.His492Leu
XM_011545294.1:c.1475A>T	XP_011543596.1:p.His492Leu
XM_011545295.1:c.935A>T	XP_011543597.1:p.His312Leu
XM_011545296.1:c.935A>T	XP_011543598.1:p.His312Leu
XM_011545294.3:c.1475A>T	XP_011543596.1:p.His492Leu
XM_011545295.2:c.935A>T	XP_011543597.1:p.His312Leu
XM_017018398.2:c.1463A>T	XP_016873887.1:p.His488Leu
XM_017018399.1:c.923A>T	XP_016873888.1:p.His308Leu
NM_031471.6:c.1463A>T MANE Select	NP_113659.3:p.His488Leu
NM_001382361.1:c.1463A>T	NP_001369290.1:p.His488Leu
NM_001382362.1:c.1475A>T	NP_001369291.1:p.His492Leu
NM_001382363.1:c.923A>T	NP_001369292.1:p.His308Leu
NM_001382364.1:c.935A>T	NP_001369293.1:p.His312Leu
NM_001382448.1:c.1463A>T	NP_001369377.1:p.His488Leu
NM_178443.3:c.1475A>T	NP_848537.1:p.His492Leu