Canonical Allele Identifier: CA381089670

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990565C>A (hg19) ; chr11:g.64223093C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223093C>A , CM000673.2:g.64223093C>A	GRCh38
NC_000011.9:g.63990565C>A , CM000673.1:g.63990565C>A	GRCh37
NC_000011.8:g.63747141C>A	NCBI36
NG_016360.1:g.21414C>A , LRG_180:g.21414C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1728C>A	ENSP00000279227.5:p.Asn576Lys
ENST00000540554.2:n.3240C>A
ENST00000541252.2:c.1176C>A	ENSP00000438885.2:p.Asn392Lys
ENST00000544997.6:c.1716C>A	ENSP00000445778.2:p.Asn572Lys
ENST00000545896.2:c.280C>A	ENSP00000440209.2:p.Pro94Thr
ENST00000546255.2:n.2020C>A
ENST00000698845.1:c.*911C>A	ENSP00000513981.1:n.*911C>A
ENST00000698846.1:n.1962C>A
ENST00000698847.1:c.*1121C>A	ENSP00000513982.1:n.*1121C>A
ENST00000698850.1:n.3737C>A
ENST00000698852.1:c.1716C>A	ENSP00000513984.1:p.Asn572Lys
ENST00000698853.1:c.*945C>A	ENSP00000513985.1:n.*945C>A
ENST00000698854.1:c.*1046C>A	ENSP00000513986.1:n.*1046C>A
ENST00000698855.1:n.3368C>A
ENST00000698856.1:n.3062C>A
ENST00000698859.1:n.2226C>A
ENST00000698860.1:c.1728C>A	ENSP00000513988.1:p.Asn576Lys
ENST00000698861.1:c.1716C>A	ENSP00000513989.1:p.Asn572Lys
ENST00000698862.1:c.*1012C>A	ENSP00000513990.1:n.*1012C>A
ENST00000698863.1:c.1716C>A	ENSP00000513991.1:p.Asn572Lys
ENST00000698864.1:n.2277C>A
ENST00000698865.1:c.1737C>A	ENSP00000513992.1:p.Asn579Lys
ENST00000698866.1:c.*1504C>A	ENSP00000513993.1:n.*1504C>A
ENST00000698867.1:n.5691C>A
ENST00000698868.1:c.1581C>A	ENSP00000513994.1:p.Asn527Lys
ENST00000698869.1:c.1482C>A	ENSP00000513995.1:p.Asn494Lys
ENST00000698870.1:c.1716C>A	ENSP00000513996.1:p.Asn572Lys
ENST00000698871.1:n.2239C>A
ENST00000698872.1:c.*505C>A	ENSP00000513997.1:n.*505C>A
ENST00000698873.1:c.*911C>A	ENSP00000513998.1:n.*911C>A
ENST00000698874.1:c.1176C>A	ENSP00000513999.1:p.Asn392Lys
ENST00000698875.1:n.1576C>A
ENST00000698876.1:n.1764C>A
ENST00000698877.1:n.1284C>A
ENST00000698878.1:c.1710C>A	ENSP00000514000.1:p.Asn570Lys
ENST00000698880.1:c.1584C>A
ENST00000345728.10:c.1716C>A MANE Select	ENSP00000339950.5:p.Asn572Lys
ENST00000279227.9:c.1728C>A	ENSP00000279227.5:p.Asn576Lys
ENST00000345728.9:c.1716C>A	ENSP00000339950.5:p.Asn572Lys
ENST00000540554.1:n.352C>A
ENST00000545896.1:c.279C>A	ENSP00000440209.1:p.Asn93Lys
NM_031471.5:c.1716C>A	NP_113659.3:p.Asn572Lys
NM_178443.2:c.1728C>A , LRG_180t1:c.1728C>A	NP_848537.1:p.Asn576Lys
XM_011545294.1:c.1728C>A	XP_011543596.1:p.Asn576Lys
XM_011545295.1:c.1188C>A	XP_011543597.1:p.Asn396Lys
XM_011545296.1:c.1188C>A	XP_011543598.1:p.Asn396Lys
XM_011545294.3:c.1728C>A	XP_011543596.1:p.Asn576Lys
XM_011545295.2:c.1188C>A	XP_011543597.1:p.Asn396Lys
XM_017018398.2:c.1716C>A	XP_016873887.1:p.Asn572Lys
XM_017018399.1:c.1176C>A	XP_016873888.1:p.Asn392Lys
NM_031471.6:c.1716C>A MANE Select	NP_113659.3:p.Asn572Lys
NM_001382361.1:c.1716C>A	NP_001369290.1:p.Asn572Lys
NM_001382362.1:c.1728C>A	NP_001369291.1:p.Asn576Lys
NM_001382363.1:c.1176C>A	NP_001369292.1:p.Asn392Lys
NM_001382364.1:c.1188C>A	NP_001369293.1:p.Asn396Lys
NM_001382448.1:c.1716C>A	NP_001369377.1:p.Asn572Lys
NM_178443.3:c.1728C>A	NP_848537.1:p.Asn576Lys