Canonical Allele Identifier: CA381089823

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990597A>G (hg19) ; chr11:g.64223125A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223125A>G , CM000673.2:g.64223125A>G	GRCh38
NC_000011.9:g.63990597A>G , CM000673.1:g.63990597A>G	GRCh37
NC_000011.8:g.63747173A>G	NCBI36
NG_016360.1:g.21446A>G , LRG_180:g.21446A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1760A>G	ENSP00000279227.5:p.Asp587Gly
ENST00000540554.2:n.3272A>G
ENST00000541252.2:c.1208A>G	ENSP00000438885.2:p.Asp403Gly
ENST00000544997.6:c.1748A>G	ENSP00000445778.2:p.Asp583Gly
ENST00000545896.2:c.312A>G	ENSP00000440209.2:p.Arg104=
ENST00000546255.2:n.2052A>G
ENST00000698845.1:c.*943A>G	ENSP00000513981.1:n.*943A>G
ENST00000698846.1:n.1994A>G
ENST00000698847.1:c.*1153A>G	ENSP00000513982.1:n.*1153A>G
ENST00000698850.1:n.3769A>G
ENST00000698852.1:c.1748A>G	ENSP00000513984.1:p.Asp583Gly
ENST00000698853.1:c.*977A>G	ENSP00000513985.1:n.*977A>G
ENST00000698854.1:c.*1078A>G	ENSP00000513986.1:n.*1078A>G
ENST00000698855.1:n.3400A>G
ENST00000698856.1:n.3094A>G
ENST00000698859.1:n.2258A>G
ENST00000698860.1:c.1760A>G	ENSP00000513988.1:p.Asp587Gly
ENST00000698861.1:c.1748A>G	ENSP00000513989.1:p.Asp583Gly
ENST00000698862.1:c.*1044A>G	ENSP00000513990.1:n.*1044A>G
ENST00000698863.1:c.1748A>G	ENSP00000513991.1:p.Asp583Gly
ENST00000698864.1:n.2309A>G
ENST00000698865.1:c.1769A>G	ENSP00000513992.1:p.Asp590Gly
ENST00000698866.1:c.*1536A>G	ENSP00000513993.1:n.*1536A>G
ENST00000698867.1:n.5723A>G
ENST00000698868.1:c.1613A>G	ENSP00000513994.1:p.Asp538Gly
ENST00000698869.1:c.1514A>G	ENSP00000513995.1:p.Asp505Gly
ENST00000698870.1:c.1748A>G	ENSP00000513996.1:p.Asp583Gly
ENST00000698871.1:n.2271A>G
ENST00000698872.1:c.*537A>G	ENSP00000513997.1:n.*537A>G
ENST00000698873.1:c.*943A>G	ENSP00000513998.1:n.*943A>G
ENST00000698874.1:c.1208A>G	ENSP00000513999.1:p.Asp403Gly
ENST00000698875.1:n.1608A>G
ENST00000698876.1:n.1796A>G
ENST00000698877.1:n.1316A>G
ENST00000698878.1:c.1742A>G	ENSP00000514000.1:p.Asp581Gly
ENST00000698880.1:c.1616A>G
ENST00000345728.10:c.1748A>G MANE Select	ENSP00000339950.5:p.Asp583Gly
ENST00000279227.9:c.1760A>G	ENSP00000279227.5:p.Asp587Gly
ENST00000345728.9:c.1748A>G	ENSP00000339950.5:p.Asp583Gly
ENST00000545896.1:c.311A>G	ENSP00000440209.1:p.Asp104Gly
NM_031471.5:c.1748A>G	NP_113659.3:p.Asp583Gly
NM_178443.2:c.1760A>G , LRG_180t1:c.1760A>G	NP_848537.1:p.Asp587Gly
XM_011545294.1:c.1760A>G	XP_011543596.1:p.Asp587Gly
XM_011545295.1:c.1220A>G	XP_011543597.1:p.Asp407Gly
XM_011545296.1:c.1220A>G	XP_011543598.1:p.Asp407Gly
XM_011545294.3:c.1760A>G	XP_011543596.1:p.Asp587Gly
XM_011545295.2:c.1220A>G	XP_011543597.1:p.Asp407Gly
XM_017018398.2:c.1748A>G	XP_016873887.1:p.Asp583Gly
XM_017018399.1:c.1208A>G	XP_016873888.1:p.Asp403Gly
NM_031471.6:c.1748A>G MANE Select	NP_113659.3:p.Asp583Gly
NM_001382361.1:c.1748A>G	NP_001369290.1:p.Asp583Gly
NM_001382362.1:c.1760A>G	NP_001369291.1:p.Asp587Gly
NM_001382363.1:c.1208A>G	NP_001369292.1:p.Asp403Gly
NM_001382364.1:c.1220A>G	NP_001369293.1:p.Asp407Gly
NM_001382448.1:c.1748A>G	NP_001369377.1:p.Asp583Gly
NM_178443.3:c.1760A>G	NP_848537.1:p.Asp587Gly