Canonical Allele Identifier: CA381090096

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990644A>G (hg19) ; chr11:g.64223172A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223172A>G , CM000673.2:g.64223172A>G	GRCh38
NC_000011.9:g.63990644A>G , CM000673.1:g.63990644A>G	GRCh37
NC_000011.8:g.63747220A>G	NCBI36
NG_016360.1:g.21493A>G , LRG_180:g.21493A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1807A>G	ENSP00000279227.5:p.Asn603Asp
ENST00000540554.2:n.3319A>G
ENST00000541252.2:c.1255A>G	ENSP00000438885.2:p.Asn419Asp
ENST00000544997.6:c.1795A>G	ENSP00000445778.2:p.Asn599Asp
ENST00000545896.2:c.359A>G	ENSP00000440209.2:p.Gln120Arg
ENST00000546255.2:n.2099A>G
ENST00000698845.1:c.*990A>G	ENSP00000513981.1:n.*990A>G
ENST00000698846.1:n.2041A>G
ENST00000698847.1:c.*1200A>G	ENSP00000513982.1:n.*1200A>G
ENST00000698850.1:n.3816A>G
ENST00000698852.1:c.1795A>G	ENSP00000513984.1:p.Asn599Asp
ENST00000698853.1:c.*1024A>G	ENSP00000513985.1:n.*1024A>G
ENST00000698854.1:c.*1125A>G	ENSP00000513986.1:n.*1125A>G
ENST00000698855.1:n.3447A>G
ENST00000698856.1:n.3141A>G
ENST00000698859.1:n.2305A>G
ENST00000698860.1:c.1807A>G	ENSP00000513988.1:p.Asn603Asp
ENST00000698861.1:c.1795A>G	ENSP00000513989.1:p.Asn599Asp
ENST00000698862.1:c.*1091A>G	ENSP00000513990.1:n.*1091A>G
ENST00000698863.1:c.1795A>G	ENSP00000513991.1:p.Asn599Asp
ENST00000698864.1:n.2356A>G
ENST00000698865.1:c.1816A>G	ENSP00000513992.1:p.Asn606Asp
ENST00000698866.1:c.*1583A>G	ENSP00000513993.1:n.*1583A>G
ENST00000698867.1:n.5770A>G
ENST00000698868.1:c.1660A>G	ENSP00000513994.1:p.Asn554Asp
ENST00000698869.1:c.1561A>G	ENSP00000513995.1:p.Asn521Asp
ENST00000698870.1:c.1795A>G	ENSP00000513996.1:p.Asn599Asp
ENST00000698871.1:n.2318A>G
ENST00000698872.1:c.*584A>G	ENSP00000513997.1:n.*584A>G
ENST00000698873.1:c.*990A>G	ENSP00000513998.1:n.*990A>G
ENST00000698874.1:c.1255A>G	ENSP00000513999.1:p.Asn419Asp
ENST00000698875.1:n.1655A>G
ENST00000698876.1:n.1843A>G
ENST00000698877.1:n.1363A>G
ENST00000698878.1:c.1789A>G	ENSP00000514000.1:p.Asn597Asp
ENST00000698880.1:c.1663A>G
ENST00000345728.10:c.1795A>G MANE Select	ENSP00000339950.5:p.Asn599Asp
ENST00000279227.9:c.1807A>G	ENSP00000279227.5:p.Asn603Asp
ENST00000345728.9:c.1795A>G	ENSP00000339950.5:p.Asn599Asp
ENST00000545896.1:c.358A>G	ENSP00000440209.1:p.Asn120Asp
NM_031471.5:c.1795A>G	NP_113659.3:p.Asn599Asp
NM_178443.2:c.1807A>G , LRG_180t1:c.1807A>G	NP_848537.1:p.Asn603Asp
XM_011545294.1:c.1807A>G	XP_011543596.1:p.Asn603Asp
XM_011545295.1:c.1267A>G	XP_011543597.1:p.Asn423Asp
XM_011545296.1:c.1267A>G	XP_011543598.1:p.Asn423Asp
XM_011545294.3:c.1807A>G	XP_011543596.1:p.Asn603Asp
XM_011545295.2:c.1267A>G	XP_011543597.1:p.Asn423Asp
XM_017018398.2:c.1795A>G	XP_016873887.1:p.Asn599Asp
XM_017018399.1:c.1255A>G	XP_016873888.1:p.Asn419Asp
NM_031471.6:c.1795A>G MANE Select	NP_113659.3:p.Asn599Asp
NM_001382361.1:c.1795A>G	NP_001369290.1:p.Asn599Asp
NM_001382362.1:c.1807A>G	NP_001369291.1:p.Asn603Asp
NM_001382363.1:c.1255A>G	NP_001369292.1:p.Asn419Asp
NM_001382364.1:c.1267A>G	NP_001369293.1:p.Asn423Asp
NM_001382448.1:c.1795A>G	NP_001369377.1:p.Asn599Asp
NM_178443.3:c.1807A>G	NP_848537.1:p.Asn603Asp