Canonical Allele Identifier: CA381090002

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990629C>G (hg19) ; chr11:g.64223157C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223157C>G , CM000673.2:g.64223157C>G	GRCh38
NC_000011.9:g.63990629C>G , CM000673.1:g.63990629C>G	GRCh37
NC_000011.8:g.63747205C>G	NCBI36
NG_016360.1:g.21478C>G , LRG_180:g.21478C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1792C>G	ENSP00000279227.5:p.Arg598Gly
ENST00000540554.2:n.3304C>G
ENST00000541252.2:c.1240C>G	ENSP00000438885.2:p.Arg414Gly
ENST00000544997.6:c.1780C>G	ENSP00000445778.2:p.Arg594Gly
ENST00000545896.2:c.344C>G	ENSP00000440209.2:p.Ala115Gly
ENST00000546255.2:n.2084C>G
ENST00000698845.1:c.*975C>G	ENSP00000513981.1:n.*975C>G
ENST00000698846.1:n.2026C>G
ENST00000698847.1:c.*1185C>G	ENSP00000513982.1:n.*1185C>G
ENST00000698850.1:n.3801C>G
ENST00000698852.1:c.1780C>G	ENSP00000513984.1:p.Arg594Gly
ENST00000698853.1:c.*1009C>G	ENSP00000513985.1:n.*1009C>G
ENST00000698854.1:c.*1110C>G	ENSP00000513986.1:n.*1110C>G
ENST00000698855.1:n.3432C>G
ENST00000698856.1:n.3126C>G
ENST00000698859.1:n.2290C>G
ENST00000698860.1:c.1792C>G	ENSP00000513988.1:p.Arg598Gly
ENST00000698861.1:c.1780C>G	ENSP00000513989.1:p.Arg594Gly
ENST00000698862.1:c.*1076C>G	ENSP00000513990.1:n.*1076C>G
ENST00000698863.1:c.1780C>G	ENSP00000513991.1:p.Arg594Gly
ENST00000698864.1:n.2341C>G
ENST00000698865.1:c.1801C>G	ENSP00000513992.1:p.Arg601Gly
ENST00000698866.1:c.*1568C>G	ENSP00000513993.1:n.*1568C>G
ENST00000698867.1:n.5755C>G
ENST00000698868.1:c.1645C>G	ENSP00000513994.1:p.Arg549Gly
ENST00000698869.1:c.1546C>G	ENSP00000513995.1:p.Arg516Gly
ENST00000698870.1:c.1780C>G	ENSP00000513996.1:p.Arg594Gly
ENST00000698871.1:n.2303C>G
ENST00000698872.1:c.*569C>G	ENSP00000513997.1:n.*569C>G
ENST00000698873.1:c.*975C>G	ENSP00000513998.1:n.*975C>G
ENST00000698874.1:c.1240C>G	ENSP00000513999.1:p.Arg414Gly
ENST00000698875.1:n.1640C>G
ENST00000698876.1:n.1828C>G
ENST00000698877.1:n.1348C>G
ENST00000698878.1:c.1774C>G	ENSP00000514000.1:p.Arg592Gly
ENST00000698880.1:c.1648C>G
ENST00000345728.10:c.1780C>G MANE Select	ENSP00000339950.5:p.Arg594Gly
ENST00000279227.9:c.1792C>G	ENSP00000279227.5:p.Arg598Gly
ENST00000345728.9:c.1780C>G	ENSP00000339950.5:p.Arg594Gly
ENST00000545896.1:c.343C>G	ENSP00000440209.1:p.Arg115Gly
NM_031471.5:c.1780C>G	NP_113659.3:p.Arg594Gly
NM_178443.2:c.1792C>G , LRG_180t1:c.1792C>G	NP_848537.1:p.Arg598Gly
XM_011545294.1:c.1792C>G	XP_011543596.1:p.Arg598Gly
XM_011545295.1:c.1252C>G	XP_011543597.1:p.Arg418Gly
XM_011545296.1:c.1252C>G	XP_011543598.1:p.Arg418Gly
XM_011545294.3:c.1792C>G	XP_011543596.1:p.Arg598Gly
XM_011545295.2:c.1252C>G	XP_011543597.1:p.Arg418Gly
XM_017018398.2:c.1780C>G	XP_016873887.1:p.Arg594Gly
XM_017018399.1:c.1240C>G	XP_016873888.1:p.Arg414Gly
NM_031471.6:c.1780C>G MANE Select	NP_113659.3:p.Arg594Gly
NM_001382361.1:c.1780C>G	NP_001369290.1:p.Arg594Gly
NM_001382362.1:c.1792C>G	NP_001369291.1:p.Arg598Gly
NM_001382363.1:c.1240C>G	NP_001369292.1:p.Arg414Gly
NM_001382364.1:c.1252C>G	NP_001369293.1:p.Arg418Gly
NM_001382448.1:c.1780C>G	NP_001369377.1:p.Arg594Gly
NM_178443.3:c.1792C>G	NP_848537.1:p.Arg598Gly