Canonical Allele Identifier: CA381089644

Gene: FERMT3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1723A>T	ENSP00000279227.5:p.Asn575Tyr
ENST00000540554.2:n.3235A>T
ENST00000541252.2:c.1171A>T	ENSP00000438885.2:p.Asn391Tyr
ENST00000544997.6:c.1711A>T	ENSP00000445778.2:p.Asn571Tyr
ENST00000545896.2:c.275A>T	ENSP00000440209.2:p.Gln92Leu
ENST00000546255.2:n.2015A>T
ENST00000698845.1:c.*906A>T	ENSP00000513981.1:n.*906A>T
ENST00000698846.1:n.1957A>T
ENST00000698847.1:c.*1116A>T	ENSP00000513982.1:n.*1116A>T
ENST00000698850.1:n.3732A>T
ENST00000698852.1:c.1711A>T	ENSP00000513984.1:p.Asn571Tyr
ENST00000698853.1:c.*940A>T	ENSP00000513985.1:n.*940A>T
ENST00000698854.1:c.*1041A>T	ENSP00000513986.1:n.*1041A>T
ENST00000698855.1:n.3363A>T
ENST00000698856.1:n.3057A>T
ENST00000698859.1:n.2221A>T
ENST00000698860.1:c.1723A>T	ENSP00000513988.1:p.Asn575Tyr
ENST00000698861.1:c.1711A>T	ENSP00000513989.1:p.Asn571Tyr
ENST00000698862.1:c.*1007A>T	ENSP00000513990.1:n.*1007A>T
ENST00000698863.1:c.1711A>T	ENSP00000513991.1:p.Asn571Tyr
ENST00000698864.1:n.2272A>T
ENST00000698865.1:c.1732A>T	ENSP00000513992.1:p.Asn578Tyr
ENST00000698866.1:c.*1499A>T	ENSP00000513993.1:n.*1499A>T
ENST00000698867.1:n.5686A>T
ENST00000698868.1:c.1576A>T	ENSP00000513994.1:p.Asn526Tyr
ENST00000698869.1:c.1477A>T	ENSP00000513995.1:p.Asn493Tyr
ENST00000698870.1:c.1711A>T	ENSP00000513996.1:p.Asn571Tyr
ENST00000698871.1:n.2234A>T
ENST00000698872.1:c.*500A>T	ENSP00000513997.1:n.*500A>T
ENST00000698873.1:c.*906A>T	ENSP00000513998.1:n.*906A>T
ENST00000698874.1:c.1171A>T	ENSP00000513999.1:p.Asn391Tyr
ENST00000698875.1:n.1571A>T
ENST00000698876.1:n.1759A>T
ENST00000698877.1:n.1279A>T
ENST00000698878.1:c.1705A>T	ENSP00000514000.1:p.Asn569Tyr
ENST00000698880.1:c.1579A>T
ENST00000345728.10:c.1711A>T MANE Select	ENSP00000339950.5:p.Asn571Tyr
ENST00000279227.9:c.1723A>T	ENSP00000279227.5:p.Asn575Tyr
ENST00000345728.9:c.1711A>T	ENSP00000339950.5:p.Asn571Tyr
ENST00000540554.1:n.347A>T
ENST00000545896.1:c.274A>T	ENSP00000440209.1:p.Asn92Tyr
NM_031471.5:c.1711A>T	NP_113659.3:p.Asn571Tyr
NM_178443.2:c.1723A>T , LRG_180t1:c.1723A>T	NP_848537.1:p.Asn575Tyr
XM_011545294.1:c.1723A>T	XP_011543596.1:p.Asn575Tyr
XM_011545295.1:c.1183A>T	XP_011543597.1:p.Asn395Tyr
XM_011545296.1:c.1183A>T	XP_011543598.1:p.Asn395Tyr
XM_011545294.3:c.1723A>T	XP_011543596.1:p.Asn575Tyr
XM_011545295.2:c.1183A>T	XP_011543597.1:p.Asn395Tyr
XM_017018398.2:c.1711A>T	XP_016873887.1:p.Asn571Tyr
XM_017018399.1:c.1171A>T	XP_016873888.1:p.Asn391Tyr
NM_031471.6:c.1711A>T MANE Select	NP_113659.3:p.Asn571Tyr
NM_001382361.1:c.1711A>T	NP_001369290.1:p.Asn571Tyr
NM_001382362.1:c.1723A>T	NP_001369291.1:p.Asn575Tyr
NM_001382363.1:c.1171A>T	NP_001369292.1:p.Asn391Tyr
NM_001382364.1:c.1183A>T	NP_001369293.1:p.Asn395Tyr
NM_001382448.1:c.1711A>T	NP_001369377.1:p.Asn571Tyr
NM_178443.3:c.1723A>T	NP_848537.1:p.Asn575Tyr