Canonical Allele Identifier: CA381087071

Gene: FERMT3

Linked Data

• gnomAD v4: 11-64220265-G-A
• MyVariant Identifiers: chr11:g.63987737G>A (hg19) ; chr11:g.64220265G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220265G>A , CM000673.2:g.64220265G>A	GRCh38
NC_000011.9:g.63987737G>A , CM000673.1:g.63987737G>A	GRCh37
NC_000011.8:g.63744313G>A	NCBI36
NG_016360.1:g.18586G>A , LRG_180:g.18586G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1262G>A	ENSP00000279227.5:p.Cys421Tyr
ENST00000540554.2:n.2319G>A
ENST00000541252.2:c.710G>A	ENSP00000438885.2:p.Cys237Tyr
ENST00000541326.6:n.562G>A
ENST00000544997.6:c.1250G>A	ENSP00000445778.2:p.Cys417Tyr
ENST00000546255.2:n.1445G>A
ENST00000698845.1:c.*445G>A	ENSP00000513981.1:n.*445G>A
ENST00000698846.1:n.1387G>A
ENST00000698847.1:c.*655G>A	ENSP00000513982.1:n.*655G>A
ENST00000698848.1:n.439G>A
ENST00000698849.1:n.370G>A
ENST00000698850.1:n.909G>A
ENST00000698852.1:c.1250G>A	ENSP00000513984.1:p.Cys417Tyr
ENST00000698853.1:c.*479G>A	ENSP00000513985.1:n.*479G>A
ENST00000698854.1:c.*580G>A	ENSP00000513986.1:n.*580G>A
ENST00000698855.1:n.2902G>A
ENST00000698856.1:n.2487G>A
ENST00000698859.1:n.1414G>A
ENST00000698860.1:c.1262G>A	ENSP00000513988.1:p.Cys421Tyr
ENST00000698861.1:c.1250G>A	ENSP00000513989.1:p.Cys417Tyr
ENST00000698862.1:c.*546G>A	ENSP00000513990.1:n.*546G>A
ENST00000698863.1:c.1250G>A	ENSP00000513991.1:p.Cys417Tyr
ENST00000698864.1:n.1356G>A
ENST00000698865.1:c.1271G>A	ENSP00000513992.1:p.Cys424Tyr
ENST00000698866.1:c.*655G>A	ENSP00000513993.1:n.*655G>A
ENST00000698867.1:n.5225G>A
ENST00000698868.1:c.1115G>A	ENSP00000513994.1:p.Cys372Tyr
ENST00000698869.1:c.1250G>A	ENSP00000513995.1:p.Cys417Tyr
ENST00000698870.1:c.1250G>A	ENSP00000513996.1:p.Cys417Tyr
ENST00000698871.1:n.1773G>A
ENST00000698872.1:c.*39G>A	ENSP00000513997.1:n.*39G>A
ENST00000698873.1:c.*445G>A	ENSP00000513998.1:n.*445G>A
ENST00000698874.1:c.710G>A	ENSP00000513999.1:p.Cys237Tyr
ENST00000698875.1:n.1110G>A
ENST00000698876.1:n.1189G>A
ENST00000698877.1:n.818G>A
ENST00000698878.1:c.1250G>A	ENSP00000514000.1:p.Cys417Tyr
ENST00000698880.1:c.1090G>A
ENST00000345728.10:c.1250G>A MANE Select	ENSP00000339950.5:p.Cys417Tyr
ENST00000279227.9:c.1262G>A	ENSP00000279227.5:p.Cys421Tyr
ENST00000345728.9:c.1250G>A	ENSP00000339950.5:p.Cys417Tyr
ENST00000540957.1:n.403G>A
ENST00000541326.5:n.557G>A
NM_031471.5:c.1250G>A	NP_113659.3:p.Cys417Tyr
NM_178443.2:c.1262G>A , LRG_180t1:c.1262G>A	NP_848537.1:p.Cys421Tyr
XM_011545294.1:c.1262G>A	XP_011543596.1:p.Cys421Tyr
XM_011545295.1:c.722G>A	XP_011543597.1:p.Cys241Tyr
XM_011545296.1:c.722G>A	XP_011543598.1:p.Cys241Tyr
XM_011545294.3:c.1262G>A	XP_011543596.1:p.Cys421Tyr
XM_011545295.2:c.722G>A	XP_011543597.1:p.Cys241Tyr
XM_017018398.2:c.1250G>A	XP_016873887.1:p.Cys417Tyr
XM_017018399.1:c.710G>A	XP_016873888.1:p.Cys237Tyr
NM_031471.6:c.1250G>A MANE Select	NP_113659.3:p.Cys417Tyr
NM_001382361.1:c.1250G>A	NP_001369290.1:p.Cys417Tyr
NM_001382362.1:c.1262G>A	NP_001369291.1:p.Cys421Tyr
NM_001382363.1:c.710G>A	NP_001369292.1:p.Cys237Tyr
NM_001382364.1:c.722G>A	NP_001369293.1:p.Cys241Tyr
NM_001382448.1:c.1250G>A	NP_001369377.1:p.Cys417Tyr
NM_178443.3:c.1262G>A	NP_848537.1:p.Cys421Tyr