Canonical Allele Identifier: CA381088143

Gene: FERMT3

Linked Data

• gnomAD v4: 11-64220607-G-T
• MyVariant Identifiers: chr11:g.63988079G>T (hg19) ; chr11:g.64220607G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220607G>T , CM000673.2:g.64220607G>T	GRCh38
NC_000011.9:g.63988079G>T , CM000673.1:g.63988079G>T	GRCh37
NC_000011.8:g.63744655G>T	NCBI36
NG_016360.1:g.18928G>T , LRG_180:g.18928G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1495G>T	ENSP00000279227.5:p.Glu499Ter
ENST00000540554.2:n.2661G>T
ENST00000541252.2:c.943G>T	ENSP00000438885.2:p.Glu315Ter
ENST00000541326.6:n.904G>T
ENST00000544997.6:c.1483G>T	ENSP00000445778.2:p.Glu495Ter
ENST00000545896.2:c.172G>T	ENSP00000440209.2:p.Glu58Ter
ENST00000546255.2:n.1787G>T
ENST00000698845.1:c.*678G>T	ENSP00000513981.1:n.*678G>T
ENST00000698846.1:n.1729G>T
ENST00000698847.1:c.*888G>T	ENSP00000513982.1:n.*888G>T
ENST00000698849.1:n.603G>T
ENST00000698850.1:n.1251G>T
ENST00000698852.1:c.1483G>T	ENSP00000513984.1:p.Glu495Ter
ENST00000698853.1:c.*712G>T	ENSP00000513985.1:n.*712G>T
ENST00000698854.1:c.*813G>T	ENSP00000513986.1:n.*813G>T
ENST00000698855.1:n.3135G>T
ENST00000698856.1:n.2829G>T
ENST00000698859.1:n.1647G>T
ENST00000698860.1:c.1495G>T	ENSP00000513988.1:p.Glu499Ter
ENST00000698861.1:c.1483G>T	ENSP00000513989.1:p.Glu495Ter
ENST00000698862.1:c.*779G>T	ENSP00000513990.1:n.*779G>T
ENST00000698863.1:c.1483G>T	ENSP00000513991.1:p.Glu495Ter
ENST00000698864.1:n.1698G>T
ENST00000698865.1:c.1504G>T	ENSP00000513992.1:p.Glu502Ter
ENST00000698866.1:c.*997G>T	ENSP00000513993.1:n.*997G>T
ENST00000698867.1:n.5458G>T
ENST00000698868.1:c.1348G>T	ENSP00000513994.1:p.Glu450Ter
ENST00000698869.1:c.1311+281G>T	ENSP00000513995.1:n.1311+281G>T
ENST00000698870.1:c.1483G>T	ENSP00000513996.1:p.Glu495Ter
ENST00000698871.1:n.2006G>T
ENST00000698872.1:c.*272G>T	ENSP00000513997.1:n.*272G>T
ENST00000698873.1:c.*678G>T	ENSP00000513998.1:n.*678G>T
ENST00000698874.1:c.943G>T	ENSP00000513999.1:p.Glu315Ter
ENST00000698875.1:n.1343G>T
ENST00000698876.1:n.1531G>T
ENST00000698877.1:n.1051G>T
ENST00000698878.1:c.1477G>T	ENSP00000514000.1:p.Glu493Ter
ENST00000698880.1:c.1351G>T
ENST00000345728.10:c.1483G>T MANE Select	ENSP00000339950.5:p.Glu495Ter
ENST00000279227.9:c.1495G>T	ENSP00000279227.5:p.Glu499Ter
ENST00000345728.9:c.1483G>T	ENSP00000339950.5:p.Glu495Ter
ENST00000545896.1:c.171G>T	ENSP00000440209.1:p.Pro57=
NM_031471.5:c.1483G>T	NP_113659.3:p.Glu495Ter
NM_178443.2:c.1495G>T , LRG_180t1:c.1495G>T	NP_848537.1:p.Glu499Ter
XM_011545294.1:c.1495G>T	XP_011543596.1:p.Glu499Ter
XM_011545295.1:c.955G>T	XP_011543597.1:p.Glu319Ter
XM_011545296.1:c.955G>T	XP_011543598.1:p.Glu319Ter
XM_011545294.3:c.1495G>T	XP_011543596.1:p.Glu499Ter
XM_011545295.2:c.955G>T	XP_011543597.1:p.Glu319Ter
XM_017018398.2:c.1483G>T	XP_016873887.1:p.Glu495Ter
XM_017018399.1:c.943G>T	XP_016873888.1:p.Glu315Ter
NM_031471.6:c.1483G>T MANE Select	NP_113659.3:p.Glu495Ter
NM_001382361.1:c.1483G>T	NP_001369290.1:p.Glu495Ter
NM_001382362.1:c.1495G>T	NP_001369291.1:p.Glu499Ter
NM_001382363.1:c.943G>T	NP_001369292.1:p.Glu315Ter
NM_001382364.1:c.955G>T	NP_001369293.1:p.Glu319Ter
NM_001382448.1:c.1483G>T	NP_001369377.1:p.Glu495Ter
NM_178443.3:c.1495G>T	NP_848537.1:p.Glu499Ter