Canonical Allele Identifier: CA381089734

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990579T>G (hg19) ; chr11:g.64223107T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223107T>G , CM000673.2:g.64223107T>G	GRCh38
NC_000011.9:g.63990579T>G , CM000673.1:g.63990579T>G	GRCh37
NC_000011.8:g.63747155T>G	NCBI36
NG_016360.1:g.21428T>G , LRG_180:g.21428T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000279227.10:c.1742T>G	ENSP00000279227.5:p.Ile581Ser
ENST00000540554.2:n.3254T>G
ENST00000541252.2:c.1190T>G	ENSP00000438885.2:p.Ile397Ser
ENST00000544997.6:c.1730T>G	ENSP00000445778.2:p.Ile577Ser
ENST00000545896.2:c.294T>G	ENSP00000440209.2:p.His98Gln
ENST00000546255.2:n.2034T>G
ENST00000698845.1:c.*925T>G	ENSP00000513981.1:n.*925T>G
ENST00000698846.1:n.1976T>G
ENST00000698847.1:c.*1135T>G	ENSP00000513982.1:n.*1135T>G
ENST00000698850.1:n.3751T>G
ENST00000698852.1:c.1730T>G	ENSP00000513984.1:p.Ile577Ser
ENST00000698853.1:c.*959T>G	ENSP00000513985.1:n.*959T>G
ENST00000698854.1:c.*1060T>G	ENSP00000513986.1:n.*1060T>G
ENST00000698855.1:n.3382T>G
ENST00000698856.1:n.3076T>G
ENST00000698859.1:n.2240T>G
ENST00000698860.1:c.1742T>G	ENSP00000513988.1:p.Ile581Ser
ENST00000698861.1:c.1730T>G	ENSP00000513989.1:p.Ile577Ser
ENST00000698862.1:c.*1026T>G	ENSP00000513990.1:n.*1026T>G
ENST00000698863.1:c.1730T>G	ENSP00000513991.1:p.Ile577Ser
ENST00000698864.1:n.2291T>G
ENST00000698865.1:c.1751T>G	ENSP00000513992.1:p.Ile584Ser
ENST00000698866.1:c.*1518T>G	ENSP00000513993.1:n.*1518T>G
ENST00000698867.1:n.5705T>G
ENST00000698868.1:c.1595T>G	ENSP00000513994.1:p.Ile532Ser
ENST00000698869.1:c.1496T>G	ENSP00000513995.1:p.Ile499Ser
ENST00000698870.1:c.1730T>G	ENSP00000513996.1:p.Ile577Ser
ENST00000698871.1:n.2253T>G
ENST00000698872.1:c.*519T>G	ENSP00000513997.1:n.*519T>G
ENST00000698873.1:c.*925T>G	ENSP00000513998.1:n.*925T>G
ENST00000698874.1:c.1190T>G	ENSP00000513999.1:p.Ile397Ser
ENST00000698875.1:n.1590T>G
ENST00000698876.1:n.1778T>G
ENST00000698877.1:n.1298T>G
ENST00000698878.1:c.1724T>G	ENSP00000514000.1:p.Ile575Ser
ENST00000698880.1:c.1598T>G
ENST00000345728.10:c.1730T>G MANE Select	ENSP00000339950.5:p.Ile577Ser
ENST00000279227.9:c.1742T>G	ENSP00000279227.5:p.Ile581Ser
ENST00000345728.9:c.1730T>G	ENSP00000339950.5:p.Ile577Ser
ENST00000540554.1:n.366T>G
ENST00000545896.1:c.293T>G	ENSP00000440209.1:p.Ile98Ser
NM_031471.5:c.1730T>G	NP_113659.3:p.Ile577Ser
NM_178443.2:c.1742T>G , LRG_180t1:c.1742T>G	NP_848537.1:p.Ile581Ser
XM_011545294.1:c.1742T>G	XP_011543596.1:p.Ile581Ser
XM_011545295.1:c.1202T>G	XP_011543597.1:p.Ile401Ser
XM_011545296.1:c.1202T>G	XP_011543598.1:p.Ile401Ser
XM_011545294.3:c.1742T>G	XP_011543596.1:p.Ile581Ser
XM_011545295.2:c.1202T>G	XP_011543597.1:p.Ile401Ser
XM_017018398.2:c.1730T>G	XP_016873887.1:p.Ile577Ser
XM_017018399.1:c.1190T>G	XP_016873888.1:p.Ile397Ser
NM_031471.6:c.1730T>G MANE Select	NP_113659.3:p.Ile577Ser
NM_001382361.1:c.1730T>G	NP_001369290.1:p.Ile577Ser
NM_001382362.1:c.1742T>G	NP_001369291.1:p.Ile581Ser
NM_001382363.1:c.1190T>G	NP_001369292.1:p.Ile397Ser
NM_001382364.1:c.1202T>G	NP_001369293.1:p.Ile401Ser
NM_001382448.1:c.1730T>G	NP_001369377.1:p.Ile577Ser
NM_178443.3:c.1742T>G	NP_848537.1:p.Ile581Ser