Canonical Allele Identifier: CA381088042

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63988067G>T (hg19) ; chr11:g.64220595G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220595G>T , CM000673.2:g.64220595G>T	GRCh38
NC_000011.9:g.63988067G>T , CM000673.1:g.63988067G>T	GRCh37
NC_000011.8:g.63744643G>T	NCBI36
NG_016360.1:g.18916G>T , LRG_180:g.18916G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1483G>T	ENSP00000279227.5:p.Asp495Tyr
ENST00000540554.2:n.2649G>T
ENST00000541252.2:c.931G>T	ENSP00000438885.2:p.Asp311Tyr
ENST00000541326.6:n.892G>T
ENST00000544997.6:c.1471G>T	ENSP00000445778.2:p.Asp491Tyr
ENST00000545896.2:c.160G>T	ENSP00000440209.2:p.Asp54Tyr
ENST00000546255.2:n.1775G>T
ENST00000698845.1:c.*666G>T	ENSP00000513981.1:n.*666G>T
ENST00000698846.1:n.1717G>T
ENST00000698847.1:c.*876G>T	ENSP00000513982.1:n.*876G>T
ENST00000698849.1:n.591G>T
ENST00000698850.1:n.1239G>T
ENST00000698852.1:c.1471G>T	ENSP00000513984.1:p.Asp491Tyr
ENST00000698853.1:c.*700G>T	ENSP00000513985.1:n.*700G>T
ENST00000698854.1:c.*801G>T	ENSP00000513986.1:n.*801G>T
ENST00000698855.1:n.3123G>T
ENST00000698856.1:n.2817G>T
ENST00000698859.1:n.1635G>T
ENST00000698860.1:c.1483G>T	ENSP00000513988.1:p.Asp495Tyr
ENST00000698861.1:c.1471G>T	ENSP00000513989.1:p.Asp491Tyr
ENST00000698862.1:c.*767G>T	ENSP00000513990.1:n.*767G>T
ENST00000698863.1:c.1471G>T	ENSP00000513991.1:p.Asp491Tyr
ENST00000698864.1:n.1686G>T
ENST00000698865.1:c.1492G>T	ENSP00000513992.1:p.Asp498Tyr
ENST00000698866.1:c.*985G>T	ENSP00000513993.1:n.*985G>T
ENST00000698867.1:n.5446G>T
ENST00000698868.1:c.1336G>T	ENSP00000513994.1:p.Asp446Tyr
ENST00000698869.1:c.1311+269G>T	ENSP00000513995.1:n.1311+269G>T
ENST00000698870.1:c.1471G>T	ENSP00000513996.1:p.Asp491Tyr
ENST00000698871.1:n.1994G>T
ENST00000698872.1:c.*260G>T	ENSP00000513997.1:n.*260G>T
ENST00000698873.1:c.*666G>T	ENSP00000513998.1:n.*666G>T
ENST00000698874.1:c.931G>T	ENSP00000513999.1:p.Asp311Tyr
ENST00000698875.1:n.1331G>T
ENST00000698876.1:n.1519G>T
ENST00000698877.1:n.1039G>T
ENST00000698878.1:c.1465G>T	ENSP00000514000.1:p.Asp489Tyr
ENST00000698880.1:c.1339G>T
ENST00000345728.10:c.1471G>T MANE Select	ENSP00000339950.5:p.Asp491Tyr
ENST00000279227.9:c.1483G>T	ENSP00000279227.5:p.Asp495Tyr
ENST00000345728.9:c.1471G>T	ENSP00000339950.5:p.Asp491Tyr
ENST00000541326.5:n.887G>T
ENST00000545896.1:c.159G>T	ENSP00000440209.1:p.Leu53=
NM_031471.5:c.1471G>T	NP_113659.3:p.Asp491Tyr
NM_178443.2:c.1483G>T , LRG_180t1:c.1483G>T	NP_848537.1:p.Asp495Tyr
XM_011545294.1:c.1483G>T	XP_011543596.1:p.Asp495Tyr
XM_011545295.1:c.943G>T	XP_011543597.1:p.Asp315Tyr
XM_011545296.1:c.943G>T	XP_011543598.1:p.Asp315Tyr
XM_011545294.3:c.1483G>T	XP_011543596.1:p.Asp495Tyr
XM_011545295.2:c.943G>T	XP_011543597.1:p.Asp315Tyr
XM_017018398.2:c.1471G>T	XP_016873887.1:p.Asp491Tyr
XM_017018399.1:c.931G>T	XP_016873888.1:p.Asp311Tyr
NM_031471.6:c.1471G>T MANE Select	NP_113659.3:p.Asp491Tyr
NM_001382361.1:c.1471G>T	NP_001369290.1:p.Asp491Tyr
NM_001382362.1:c.1483G>T	NP_001369291.1:p.Asp495Tyr
NM_001382363.1:c.931G>T	NP_001369292.1:p.Asp311Tyr
NM_001382364.1:c.943G>T	NP_001369293.1:p.Asp315Tyr
NM_001382448.1:c.1471G>T	NP_001369377.1:p.Asp491Tyr
NM_178443.3:c.1483G>T	NP_848537.1:p.Asp495Tyr