Canonical Allele Identifier: CA475151806

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990583C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223111C>T , CM000673.2:g.64223111C>T	GRCh38
NC_000011.9:g.63990583C>T , CM000673.1:g.63990583C>T	GRCh37
NC_000011.8:g.63747159C>T	NCBI36
NG_016360.1:g.21432C>T , LRG_180:g.21432C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1746C>T	ENSP00000279227.5:p.Asp582=
ENST00000540554.2:n.3258C>T
ENST00000541252.2:c.1194C>T	ENSP00000438885.2:p.Asp398=
ENST00000544997.6:c.1734C>T	ENSP00000445778.2:p.Asp578=
ENST00000545896.2:c.298C>T	ENSP00000440209.2:p.Leu100Phe
ENST00000546255.2:n.2038C>T
ENST00000698845.1:c.*929C>T	ENSP00000513981.1:n.*929C>T
ENST00000698846.1:n.1980C>T
ENST00000698847.1:c.*1139C>T	ENSP00000513982.1:n.*1139C>T
ENST00000698850.1:n.3755C>T
ENST00000698852.1:c.1734C>T	ENSP00000513984.1:p.Asp578=
ENST00000698853.1:c.*963C>T	ENSP00000513985.1:n.*963C>T
ENST00000698854.1:c.*1064C>T	ENSP00000513986.1:n.*1064C>T
ENST00000698855.1:n.3386C>T
ENST00000698856.1:n.3080C>T
ENST00000698859.1:n.2244C>T
ENST00000698860.1:c.1746C>T	ENSP00000513988.1:p.Asp582=
ENST00000698861.1:c.1734C>T	ENSP00000513989.1:p.Asp578=
ENST00000698862.1:c.*1030C>T	ENSP00000513990.1:n.*1030C>T
ENST00000698863.1:c.1734C>T	ENSP00000513991.1:p.Asp578=
ENST00000698864.1:n.2295C>T
ENST00000698865.1:c.1755C>T	ENSP00000513992.1:p.Asp585=
ENST00000698866.1:c.*1522C>T	ENSP00000513993.1:n.*1522C>T
ENST00000698867.1:n.5709C>T
ENST00000698868.1:c.1599C>T	ENSP00000513994.1:p.Asp533=
ENST00000698869.1:c.1500C>T	ENSP00000513995.1:p.Asp500=
ENST00000698870.1:c.1734C>T	ENSP00000513996.1:p.Asp578=
ENST00000698871.1:n.2257C>T
ENST00000698872.1:c.*523C>T	ENSP00000513997.1:n.*523C>T
ENST00000698873.1:c.*929C>T	ENSP00000513998.1:n.*929C>T
ENST00000698874.1:c.1194C>T	ENSP00000513999.1:p.Asp398=
ENST00000698875.1:n.1594C>T
ENST00000698876.1:n.1782C>T
ENST00000698877.1:n.1302C>T
ENST00000698878.1:c.1728C>T	ENSP00000514000.1:p.Asp576=
ENST00000698880.1:c.1602C>T
ENST00000345728.10:c.1734C>T MANE Select	ENSP00000339950.5:p.Asp578=
ENST00000279227.9:c.1746C>T	ENSP00000279227.5:p.Asp582=
ENST00000345728.9:c.1734C>T	ENSP00000339950.5:p.Asp578=
ENST00000540554.1:n.370C>T
ENST00000545896.1:c.297C>T	ENSP00000440209.1:p.Asp99=
NM_031471.5:c.1734C>T	NP_113659.3:p.Asp578=
NM_178443.2:c.1746C>T , LRG_180t1:c.1746C>T	NP_848537.1:p.Asp582=
XM_011545294.1:c.1746C>T	XP_011543596.1:p.Asp582=
XM_011545295.1:c.1206C>T	XP_011543597.1:p.Asp402=
XM_011545296.1:c.1206C>T	XP_011543598.1:p.Asp402=
XM_011545294.3:c.1746C>T	XP_011543596.1:p.Asp582=
XM_011545295.2:c.1206C>T	XP_011543597.1:p.Asp402=
XM_017018398.2:c.1734C>T	XP_016873887.1:p.Asp578=
XM_017018399.1:c.1194C>T	XP_016873888.1:p.Asp398=
NM_031471.6:c.1734C>T MANE Select	NP_113659.3:p.Asp578=
NM_001382361.1:c.1734C>T	NP_001369290.1:p.Asp578=
NM_001382362.1:c.1746C>T	NP_001369291.1:p.Asp582=
NM_001382363.1:c.1194C>T	NP_001369292.1:p.Asp398=
NM_001382364.1:c.1206C>T	NP_001369293.1:p.Asp402=
NM_001382448.1:c.1734C>T	NP_001369377.1:p.Asp578=
NM_178443.3:c.1746C>T	NP_848537.1:p.Asp582=