Canonical Allele Identifier: CA381089642

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990560A>G (hg19) ; chr11:g.64223088A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223088A>G , CM000673.2:g.64223088A>G	GRCh38
NC_000011.9:g.63990560A>G , CM000673.1:g.63990560A>G	GRCh37
NC_000011.8:g.63747136A>G	NCBI36
NG_016360.1:g.21409A>G , LRG_180:g.21409A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1723A>G	ENSP00000279227.5:p.Asn575Asp
ENST00000540554.2:n.3235A>G
ENST00000541252.2:c.1171A>G	ENSP00000438885.2:p.Asn391Asp
ENST00000544997.6:c.1711A>G	ENSP00000445778.2:p.Asn571Asp
ENST00000545896.2:c.275A>G	ENSP00000440209.2:p.Gln92Arg
ENST00000546255.2:n.2015A>G
ENST00000698845.1:c.*906A>G	ENSP00000513981.1:n.*906A>G
ENST00000698846.1:n.1957A>G
ENST00000698847.1:c.*1116A>G	ENSP00000513982.1:n.*1116A>G
ENST00000698850.1:n.3732A>G
ENST00000698852.1:c.1711A>G	ENSP00000513984.1:p.Asn571Asp
ENST00000698853.1:c.*940A>G	ENSP00000513985.1:n.*940A>G
ENST00000698854.1:c.*1041A>G	ENSP00000513986.1:n.*1041A>G
ENST00000698855.1:n.3363A>G
ENST00000698856.1:n.3057A>G
ENST00000698859.1:n.2221A>G
ENST00000698860.1:c.1723A>G	ENSP00000513988.1:p.Asn575Asp
ENST00000698861.1:c.1711A>G	ENSP00000513989.1:p.Asn571Asp
ENST00000698862.1:c.*1007A>G	ENSP00000513990.1:n.*1007A>G
ENST00000698863.1:c.1711A>G	ENSP00000513991.1:p.Asn571Asp
ENST00000698864.1:n.2272A>G
ENST00000698865.1:c.1732A>G	ENSP00000513992.1:p.Asn578Asp
ENST00000698866.1:c.*1499A>G	ENSP00000513993.1:n.*1499A>G
ENST00000698867.1:n.5686A>G
ENST00000698868.1:c.1576A>G	ENSP00000513994.1:p.Asn526Asp
ENST00000698869.1:c.1477A>G	ENSP00000513995.1:p.Asn493Asp
ENST00000698870.1:c.1711A>G	ENSP00000513996.1:p.Asn571Asp
ENST00000698871.1:n.2234A>G
ENST00000698872.1:c.*500A>G	ENSP00000513997.1:n.*500A>G
ENST00000698873.1:c.*906A>G	ENSP00000513998.1:n.*906A>G
ENST00000698874.1:c.1171A>G	ENSP00000513999.1:p.Asn391Asp
ENST00000698875.1:n.1571A>G
ENST00000698876.1:n.1759A>G
ENST00000698877.1:n.1279A>G
ENST00000698878.1:c.1705A>G	ENSP00000514000.1:p.Asn569Asp
ENST00000698880.1:c.1579A>G
ENST00000345728.10:c.1711A>G MANE Select	ENSP00000339950.5:p.Asn571Asp
ENST00000279227.9:c.1723A>G	ENSP00000279227.5:p.Asn575Asp
ENST00000345728.9:c.1711A>G	ENSP00000339950.5:p.Asn571Asp
ENST00000540554.1:n.347A>G
ENST00000545896.1:c.274A>G	ENSP00000440209.1:p.Asn92Asp
NM_031471.5:c.1711A>G	NP_113659.3:p.Asn571Asp
NM_178443.2:c.1723A>G , LRG_180t1:c.1723A>G	NP_848537.1:p.Asn575Asp
XM_011545294.1:c.1723A>G	XP_011543596.1:p.Asn575Asp
XM_011545295.1:c.1183A>G	XP_011543597.1:p.Asn395Asp
XM_011545296.1:c.1183A>G	XP_011543598.1:p.Asn395Asp
XM_011545294.3:c.1723A>G	XP_011543596.1:p.Asn575Asp
XM_011545295.2:c.1183A>G	XP_011543597.1:p.Asn395Asp
XM_017018398.2:c.1711A>G	XP_016873887.1:p.Asn571Asp
XM_017018399.1:c.1171A>G	XP_016873888.1:p.Asn391Asp
NM_031471.6:c.1711A>G MANE Select	NP_113659.3:p.Asn571Asp
NM_001382361.1:c.1711A>G	NP_001369290.1:p.Asn571Asp
NM_001382362.1:c.1723A>G	NP_001369291.1:p.Asn575Asp
NM_001382363.1:c.1171A>G	NP_001369292.1:p.Asn391Asp
NM_001382364.1:c.1183A>G	NP_001369293.1:p.Asn395Asp
NM_001382448.1:c.1711A>G	NP_001369377.1:p.Asn571Asp
NM_178443.3:c.1723A>G	NP_848537.1:p.Asn575Asp