Canonical Allele Identifier: CA381083095

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63979143T>G (hg19) ; chr11:g.64211671T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64211671T>G , CM000673.2:g.64211671T>G	GRCh38
NC_000011.9:g.63979143T>G , CM000673.1:g.63979143T>G	GRCh37
NC_000011.8:g.63735719T>G	NCBI36
NG_016360.1:g.9992T>G , LRG_180:g.9992T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.710T>G	ENSP00000279227.5:p.Met237Arg
ENST00000541252.2:c.170T>G	ENSP00000438885.2:p.Met57Arg
ENST00000541326.6:n.27T>G
ENST00000544997.6:c.710T>G	ENSP00000445778.2:p.Met237Arg
ENST00000546255.2:n.804T>G
ENST00000698845.1:c.710T>G	ENSP00000513981.1:p.Met237Arg
ENST00000698846.1:n.847T>G
ENST00000698847.1:c.*115T>G	ENSP00000513982.1:n.*115T>G
ENST00000698850.1:n.22T>G
ENST00000698852.1:c.710T>G	ENSP00000513984.1:p.Met237Arg
ENST00000698853.1:c.710T>G	ENSP00000513985.1:p.Met237Arg
ENST00000698854.1:c.710T>G	ENSP00000513986.1:p.Met237Arg
ENST00000698855.1:n.2362T>G
ENST00000698856.1:n.1630T>G
ENST00000698859.1:n.874T>G
ENST00000698860.1:c.710T>G	ENSP00000513988.1:p.Met237Arg
ENST00000698861.1:c.710T>G	ENSP00000513989.1:p.Met237Arg
ENST00000698862.1:c.710T>G	ENSP00000513990.1:p.Met237Arg
ENST00000698863.1:c.710T>G	ENSP00000513991.1:p.Met237Arg
ENST00000698864.1:n.816T>G
ENST00000698865.1:c.710T>G	ENSP00000513992.1:p.Met237Arg
ENST00000698866.1:c.*115T>G	ENSP00000513993.1:n.*115T>G
ENST00000698867.1:n.4419T>G
ENST00000698868.1:c.710T>G	ENSP00000513994.1:p.Met237Arg
ENST00000698869.1:c.710T>G	ENSP00000513995.1:p.Met237Arg
ENST00000698870.1:c.710T>G	ENSP00000513996.1:p.Met237Arg
ENST00000698871.1:n.967T>G
ENST00000698872.1:c.170T>G	ENSP00000513997.1:p.Met57Arg
ENST00000698873.1:c.170T>G	ENSP00000513998.1:p.Met57Arg
ENST00000698874.1:c.170T>G	ENSP00000513999.1:p.Met57Arg
ENST00000698875.1:n.570T>G
ENST00000698878.1:c.710T>G	ENSP00000514000.1:p.Met237Arg
ENST00000698879.1:c.619T>G
ENST00000698880.1:c.550T>G
ENST00000345728.10:c.710T>G MANE Select	ENSP00000339950.5:p.Met237Arg
ENST00000279227.9:c.710T>G	ENSP00000279227.5:p.Met237Arg
ENST00000345728.9:c.710T>G	ENSP00000339950.5:p.Met237Arg
ENST00000541252.1:c.170T>G	ENSP00000438885.1:p.Met57Arg
ENST00000541326.5:n.22T>G
ENST00000544997.5:c.710T>G	ENSP00000445778.1:p.Met237Arg
NM_031471.5:c.710T>G	NP_113659.3:p.Met237Arg
NM_178443.2:c.710T>G , LRG_180t1:c.710T>G	NP_848537.1:p.Met237Arg
XM_011545294.1:c.710T>G	XP_011543596.1:p.Met237Arg
XM_011545295.1:c.170T>G	XP_011543597.1:p.Met57Arg
XM_011545296.1:c.170T>G	XP_011543598.1:p.Met57Arg
XM_011545294.3:c.710T>G	XP_011543596.1:p.Met237Arg
XM_011545295.2:c.170T>G	XP_011543597.1:p.Met57Arg
XM_017018398.2:c.710T>G	XP_016873887.1:p.Met237Arg
XM_017018399.1:c.170T>G	XP_016873888.1:p.Met57Arg
NM_031471.6:c.710T>G MANE Select	NP_113659.3:p.Met237Arg
NM_001382361.1:c.710T>G	NP_001369290.1:p.Met237Arg
NM_001382362.1:c.710T>G	NP_001369291.1:p.Met237Arg
NM_001382363.1:c.170T>G	NP_001369292.1:p.Met57Arg
NM_001382364.1:c.170T>G	NP_001369293.1:p.Met57Arg
NM_001382448.1:c.710T>G	NP_001369377.1:p.Met237Arg
NM_178443.3:c.710T>G	NP_848537.1:p.Met237Arg