Canonical Allele Identifier: CA381089706

Gene: FERMT3

Linked Data

• gnomAD v4: 11-64223101-T-A
• MyVariant Identifiers: chr11:g.63990573T>A (hg19) ; chr11:g.64223101T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223101T>A , CM000673.2:g.64223101T>A	GRCh38
NC_000011.9:g.63990573T>A , CM000673.1:g.63990573T>A	GRCh37
NC_000011.8:g.63747149T>A	NCBI36
NG_016360.1:g.21422T>A , LRG_180:g.21422T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000279227.10:c.1736T>A	ENSP00000279227.5:p.Ile579Asn
ENST00000540554.2:n.3248T>A
ENST00000541252.2:c.1184T>A	ENSP00000438885.2:p.Ile395Asn
ENST00000544997.6:c.1724T>A	ENSP00000445778.2:p.Ile575Asn
ENST00000545896.2:c.288T>A	ENSP00000440209.2:p.Asp96Glu
ENST00000546255.2:n.2028T>A
ENST00000698845.1:c.*919T>A	ENSP00000513981.1:n.*919T>A
ENST00000698846.1:n.1970T>A
ENST00000698847.1:c.*1129T>A	ENSP00000513982.1:n.*1129T>A
ENST00000698850.1:n.3745T>A
ENST00000698852.1:c.1724T>A	ENSP00000513984.1:p.Ile575Asn
ENST00000698853.1:c.*953T>A	ENSP00000513985.1:n.*953T>A
ENST00000698854.1:c.*1054T>A	ENSP00000513986.1:n.*1054T>A
ENST00000698855.1:n.3376T>A
ENST00000698856.1:n.3070T>A
ENST00000698859.1:n.2234T>A
ENST00000698860.1:c.1736T>A	ENSP00000513988.1:p.Ile579Asn
ENST00000698861.1:c.1724T>A	ENSP00000513989.1:p.Ile575Asn
ENST00000698862.1:c.*1020T>A	ENSP00000513990.1:n.*1020T>A
ENST00000698863.1:c.1724T>A	ENSP00000513991.1:p.Ile575Asn
ENST00000698864.1:n.2285T>A
ENST00000698865.1:c.1745T>A	ENSP00000513992.1:p.Ile582Asn
ENST00000698866.1:c.*1512T>A	ENSP00000513993.1:n.*1512T>A
ENST00000698867.1:n.5699T>A
ENST00000698868.1:c.1589T>A	ENSP00000513994.1:p.Ile530Asn
ENST00000698869.1:c.1490T>A	ENSP00000513995.1:p.Ile497Asn
ENST00000698870.1:c.1724T>A	ENSP00000513996.1:p.Ile575Asn
ENST00000698871.1:n.2247T>A
ENST00000698872.1:c.*513T>A	ENSP00000513997.1:n.*513T>A
ENST00000698873.1:c.*919T>A	ENSP00000513998.1:n.*919T>A
ENST00000698874.1:c.1184T>A	ENSP00000513999.1:p.Ile395Asn
ENST00000698875.1:n.1584T>A
ENST00000698876.1:n.1772T>A
ENST00000698877.1:n.1292T>A
ENST00000698878.1:c.1718T>A	ENSP00000514000.1:p.Ile573Asn
ENST00000698880.1:c.1592T>A
ENST00000345728.10:c.1724T>A MANE Select	ENSP00000339950.5:p.Ile575Asn
ENST00000279227.9:c.1736T>A	ENSP00000279227.5:p.Ile579Asn
ENST00000345728.9:c.1724T>A	ENSP00000339950.5:p.Ile575Asn
ENST00000540554.1:n.360T>A
ENST00000545896.1:c.287T>A	ENSP00000440209.1:p.Ile96Asn
NM_031471.5:c.1724T>A	NP_113659.3:p.Ile575Asn
NM_178443.2:c.1736T>A , LRG_180t1:c.1736T>A	NP_848537.1:p.Ile579Asn
XM_011545294.1:c.1736T>A	XP_011543596.1:p.Ile579Asn
XM_011545295.1:c.1196T>A	XP_011543597.1:p.Ile399Asn
XM_011545296.1:c.1196T>A	XP_011543598.1:p.Ile399Asn
XM_011545294.3:c.1736T>A	XP_011543596.1:p.Ile579Asn
XM_011545295.2:c.1196T>A	XP_011543597.1:p.Ile399Asn
XM_017018398.2:c.1724T>A	XP_016873887.1:p.Ile575Asn
XM_017018399.1:c.1184T>A	XP_016873888.1:p.Ile395Asn
NM_031471.6:c.1724T>A MANE Select	NP_113659.3:p.Ile575Asn
NM_001382361.1:c.1724T>A	NP_001369290.1:p.Ile575Asn
NM_001382362.1:c.1736T>A	NP_001369291.1:p.Ile579Asn
NM_001382363.1:c.1184T>A	NP_001369292.1:p.Ile395Asn
NM_001382364.1:c.1196T>A	NP_001369293.1:p.Ile399Asn
NM_001382448.1:c.1724T>A	NP_001369377.1:p.Ile575Asn
NM_178443.3:c.1736T>A	NP_848537.1:p.Ile579Asn