Canonical Allele Identifier: CA381090186

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990659C>G (hg19) ; chr11:g.64223187C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223187C>G , CM000673.2:g.64223187C>G	GRCh38
NC_000011.9:g.63990659C>G , CM000673.1:g.63990659C>G	GRCh37
NC_000011.8:g.63747235C>G	NCBI36
NG_016360.1:g.21508C>G , LRG_180:g.21508C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1822C>G	ENSP00000279227.5:p.Gln608Glu
ENST00000540554.2:n.3334C>G
ENST00000541252.2:c.1270C>G	ENSP00000438885.2:p.Gln424Glu
ENST00000544997.6:c.1810C>G	ENSP00000445778.2:p.Gln604Glu
ENST00000545896.2:c.374C>G	ENSP00000440209.2:p.Ala125Gly
ENST00000546255.2:n.2114C>G
ENST00000698845.1:c.*1005C>G	ENSP00000513981.1:n.*1005C>G
ENST00000698846.1:n.2056C>G
ENST00000698847.1:c.*1215C>G	ENSP00000513982.1:n.*1215C>G
ENST00000698850.1:n.3831C>G
ENST00000698852.1:c.1810C>G	ENSP00000513984.1:p.Gln604Glu
ENST00000698853.1:c.*1039C>G	ENSP00000513985.1:n.*1039C>G
ENST00000698854.1:c.*1140C>G	ENSP00000513986.1:n.*1140C>G
ENST00000698855.1:n.3462C>G
ENST00000698856.1:n.3156C>G
ENST00000698859.1:n.2320C>G
ENST00000698860.1:c.1822C>G	ENSP00000513988.1:p.Gln608Glu
ENST00000698861.1:c.1810C>G	ENSP00000513989.1:p.Gln604Glu
ENST00000698862.1:c.*1106C>G	ENSP00000513990.1:n.*1106C>G
ENST00000698863.1:c.1810C>G	ENSP00000513991.1:p.Gln604Glu
ENST00000698864.1:n.2371C>G
ENST00000698865.1:c.1831C>G	ENSP00000513992.1:p.Gln611Glu
ENST00000698866.1:c.*1598C>G	ENSP00000513993.1:n.*1598C>G
ENST00000698867.1:n.5785C>G
ENST00000698868.1:c.1675C>G	ENSP00000513994.1:p.Gln559Glu
ENST00000698869.1:c.1576C>G	ENSP00000513995.1:p.Gln526Glu
ENST00000698870.1:c.1810C>G	ENSP00000513996.1:p.Gln604Glu
ENST00000698871.1:n.2333C>G
ENST00000698872.1:c.*599C>G	ENSP00000513997.1:n.*599C>G
ENST00000698873.1:c.*1005C>G	ENSP00000513998.1:n.*1005C>G
ENST00000698874.1:c.1270C>G	ENSP00000513999.1:p.Gln424Glu
ENST00000698875.1:n.1670C>G
ENST00000698876.1:n.1858C>G
ENST00000698877.1:n.1378C>G
ENST00000698878.1:c.1804C>G	ENSP00000514000.1:p.Gln602Glu
ENST00000698880.1:c.1678C>G
ENST00000345728.10:c.1810C>G MANE Select	ENSP00000339950.5:p.Gln604Glu
ENST00000279227.9:c.1822C>G	ENSP00000279227.5:p.Gln608Glu
ENST00000345728.9:c.1810C>G	ENSP00000339950.5:p.Gln604Glu
ENST00000545896.1:c.373C>G	ENSP00000440209.1:p.Gln125Glu
NM_031471.5:c.1810C>G	NP_113659.3:p.Gln604Glu
NM_178443.2:c.1822C>G , LRG_180t1:c.1822C>G	NP_848537.1:p.Gln608Glu
XM_011545294.1:c.1822C>G	XP_011543596.1:p.Gln608Glu
XM_011545295.1:c.1282C>G	XP_011543597.1:p.Gln428Glu
XM_011545296.1:c.1282C>G	XP_011543598.1:p.Gln428Glu
XM_011545294.3:c.1822C>G	XP_011543596.1:p.Gln608Glu
XM_011545295.2:c.1282C>G	XP_011543597.1:p.Gln428Glu
XM_017018398.2:c.1810C>G	XP_016873887.1:p.Gln604Glu
XM_017018399.1:c.1270C>G	XP_016873888.1:p.Gln424Glu
NM_031471.6:c.1810C>G MANE Select	NP_113659.3:p.Gln604Glu
NM_001382361.1:c.1810C>G	NP_001369290.1:p.Gln604Glu
NM_001382362.1:c.1822C>G	NP_001369291.1:p.Gln608Glu
NM_001382363.1:c.1270C>G	NP_001369292.1:p.Gln424Glu
NM_001382364.1:c.1282C>G	NP_001369293.1:p.Gln428Glu
NM_001382448.1:c.1810C>G	NP_001369377.1:p.Gln604Glu
NM_178443.3:c.1822C>G	NP_848537.1:p.Gln608Glu