Canonical Allele Identifier: CA381087107

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987746T>G (hg19) ; chr11:g.64220274T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220274T>G , CM000673.2:g.64220274T>G	GRCh38
NC_000011.9:g.63987746T>G , CM000673.1:g.63987746T>G	GRCh37
NC_000011.8:g.63744322T>G	NCBI36
NG_016360.1:g.18595T>G , LRG_180:g.18595T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1271T>G	ENSP00000279227.5:p.Leu424Arg
ENST00000540554.2:n.2328T>G
ENST00000541252.2:c.719T>G	ENSP00000438885.2:p.Leu240Arg
ENST00000541326.6:n.571T>G
ENST00000544997.6:c.1259T>G	ENSP00000445778.2:p.Leu420Arg
ENST00000546255.2:n.1454T>G
ENST00000698845.1:c.*454T>G	ENSP00000513981.1:n.*454T>G
ENST00000698846.1:n.1396T>G
ENST00000698847.1:c.*664T>G	ENSP00000513982.1:n.*664T>G
ENST00000698848.1:n.448T>G
ENST00000698849.1:n.379T>G
ENST00000698850.1:n.918T>G
ENST00000698852.1:c.1259T>G	ENSP00000513984.1:p.Leu420Arg
ENST00000698853.1:c.*488T>G	ENSP00000513985.1:n.*488T>G
ENST00000698854.1:c.*589T>G	ENSP00000513986.1:n.*589T>G
ENST00000698855.1:n.2911T>G
ENST00000698856.1:n.2496T>G
ENST00000698859.1:n.1423T>G
ENST00000698860.1:c.1271T>G	ENSP00000513988.1:p.Leu424Arg
ENST00000698861.1:c.1259T>G	ENSP00000513989.1:p.Leu420Arg
ENST00000698862.1:c.*555T>G	ENSP00000513990.1:n.*555T>G
ENST00000698863.1:c.1259T>G	ENSP00000513991.1:p.Leu420Arg
ENST00000698864.1:n.1365T>G
ENST00000698865.1:c.1280T>G	ENSP00000513992.1:p.Leu427Arg
ENST00000698866.1:c.*664T>G	ENSP00000513993.1:n.*664T>G
ENST00000698867.1:n.5234T>G
ENST00000698868.1:c.1124T>G	ENSP00000513994.1:p.Leu375Arg
ENST00000698869.1:c.1259T>G	ENSP00000513995.1:p.Leu420Arg
ENST00000698870.1:c.1259T>G	ENSP00000513996.1:p.Leu420Arg
ENST00000698871.1:n.1782T>G
ENST00000698872.1:c.*48T>G	ENSP00000513997.1:n.*48T>G
ENST00000698873.1:c.*454T>G	ENSP00000513998.1:n.*454T>G
ENST00000698874.1:c.719T>G	ENSP00000513999.1:p.Leu240Arg
ENST00000698875.1:n.1119T>G
ENST00000698876.1:n.1198T>G
ENST00000698877.1:n.827T>G
ENST00000698878.1:c.1259T>G	ENSP00000514000.1:p.Leu420Arg
ENST00000698880.1:c.1099T>G
ENST00000345728.10:c.1259T>G MANE Select	ENSP00000339950.5:p.Leu420Arg
ENST00000279227.9:c.1271T>G	ENSP00000279227.5:p.Leu424Arg
ENST00000345728.9:c.1259T>G	ENSP00000339950.5:p.Leu420Arg
ENST00000540957.1:n.412T>G
ENST00000541326.5:n.566T>G
NM_031471.5:c.1259T>G	NP_113659.3:p.Leu420Arg
NM_178443.2:c.1271T>G , LRG_180t1:c.1271T>G	NP_848537.1:p.Leu424Arg
XM_011545294.1:c.1271T>G	XP_011543596.1:p.Leu424Arg
XM_011545295.1:c.731T>G	XP_011543597.1:p.Leu244Arg
XM_011545296.1:c.731T>G	XP_011543598.1:p.Leu244Arg
XM_011545294.3:c.1271T>G	XP_011543596.1:p.Leu424Arg
XM_011545295.2:c.731T>G	XP_011543597.1:p.Leu244Arg
XM_017018398.2:c.1259T>G	XP_016873887.1:p.Leu420Arg
XM_017018399.1:c.719T>G	XP_016873888.1:p.Leu240Arg
NM_031471.6:c.1259T>G MANE Select	NP_113659.3:p.Leu420Arg
NM_001382361.1:c.1259T>G	NP_001369290.1:p.Leu420Arg
NM_001382362.1:c.1271T>G	NP_001369291.1:p.Leu424Arg
NM_001382363.1:c.719T>G	NP_001369292.1:p.Leu240Arg
NM_001382364.1:c.731T>G	NP_001369293.1:p.Leu244Arg
NM_001382448.1:c.1259T>G	NP_001369377.1:p.Leu420Arg
NM_178443.3:c.1271T>G	NP_848537.1:p.Leu424Arg