Canonical Allele Identifier: CA381088436

Gene: FERMT3

Linked Data

• dbSNP Id: rs1452741056
• gnomAD v2: 11-63988113-G-A
• gnomAD v3: 11-64220641-G-A
• gnomAD v4: 11-64220641-G-A
• MyVariant Identifiers: chr11:g.63988113G>A (hg19) ; chr11:g.64220641G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220641G>A , CM000673.2:g.64220641G>A	GRCh38
NC_000011.9:g.63988113G>A , CM000673.1:g.63988113G>A	GRCh37
NC_000011.8:g.63744689G>A	NCBI36
NG_016360.1:g.18962G>A , LRG_180:g.18962G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1529G>A	ENSP00000279227.5:p.Arg510His
ENST00000540554.2:n.2695G>A
ENST00000541252.2:c.977G>A	ENSP00000438885.2:p.Arg326His
ENST00000541326.6:n.938G>A
ENST00000544997.6:c.1517G>A	ENSP00000445778.2:p.Arg506His
ENST00000545896.2:c.206G>A	ENSP00000440209.2:p.Arg69His
ENST00000546255.2:n.1821G>A
ENST00000698845.1:c.*712G>A	ENSP00000513981.1:n.*712G>A
ENST00000698846.1:n.1763G>A
ENST00000698847.1:c.*922G>A	ENSP00000513982.1:n.*922G>A
ENST00000698849.1:n.637G>A
ENST00000698850.1:n.1285G>A
ENST00000698852.1:c.1517G>A	ENSP00000513984.1:p.Arg506His
ENST00000698853.1:c.*746G>A	ENSP00000513985.1:n.*746G>A
ENST00000698854.1:c.*847G>A	ENSP00000513986.1:n.*847G>A
ENST00000698855.1:n.3169G>A
ENST00000698856.1:n.2863G>A
ENST00000698859.1:n.1681G>A
ENST00000698860.1:c.1529G>A	ENSP00000513988.1:p.Arg510His
ENST00000698861.1:c.1517G>A	ENSP00000513989.1:p.Arg506His
ENST00000698862.1:c.*813G>A	ENSP00000513990.1:n.*813G>A
ENST00000698863.1:c.1517G>A	ENSP00000513991.1:p.Arg506His
ENST00000698864.1:n.1732G>A
ENST00000698865.1:c.1538G>A	ENSP00000513992.1:p.Arg513His
ENST00000698866.1:c.*1031G>A	ENSP00000513993.1:n.*1031G>A
ENST00000698867.1:n.5492G>A
ENST00000698868.1:c.1382G>A	ENSP00000513994.1:p.Arg461His
ENST00000698869.1:c.1311+315G>A	ENSP00000513995.1:n.1311+315G>A
ENST00000698870.1:c.1517G>A	ENSP00000513996.1:p.Arg506His
ENST00000698871.1:n.2040G>A
ENST00000698872.1:c.*306G>A	ENSP00000513997.1:n.*306G>A
ENST00000698873.1:c.*712G>A	ENSP00000513998.1:n.*712G>A
ENST00000698874.1:c.977G>A	ENSP00000513999.1:p.Arg326His
ENST00000698875.1:n.1377G>A
ENST00000698876.1:n.1565G>A
ENST00000698877.1:n.1085G>A
ENST00000698878.1:c.1511G>A	ENSP00000514000.1:p.Arg504His
ENST00000698880.1:c.1385G>A
ENST00000345728.10:c.1517G>A MANE Select	ENSP00000339950.5:p.Arg506His
ENST00000279227.9:c.1529G>A	ENSP00000279227.5:p.Arg510His
ENST00000345728.9:c.1517G>A	ENSP00000339950.5:p.Arg506His
ENST00000545896.1:c.205G>A	ENSP00000440209.1:p.Val69Ile
NM_031471.5:c.1517G>A	NP_113659.3:p.Arg506His
NM_178443.2:c.1529G>A , LRG_180t1:c.1529G>A	NP_848537.1:p.Arg510His
XM_011545294.1:c.1529G>A	XP_011543596.1:p.Arg510His
XM_011545295.1:c.989G>A	XP_011543597.1:p.Arg330His
XM_011545296.1:c.989G>A	XP_011543598.1:p.Arg330His
XM_011545294.3:c.1529G>A	XP_011543596.1:p.Arg510His
XM_011545295.2:c.989G>A	XP_011543597.1:p.Arg330His
XM_017018398.2:c.1517G>A	XP_016873887.1:p.Arg506His
XM_017018399.1:c.977G>A	XP_016873888.1:p.Arg326His
NM_031471.6:c.1517G>A MANE Select	NP_113659.3:p.Arg506His
NM_001382361.1:c.1517G>A	NP_001369290.1:p.Arg506His
NM_001382362.1:c.1529G>A	NP_001369291.1:p.Arg510His
NM_001382363.1:c.977G>A	NP_001369292.1:p.Arg326His
NM_001382364.1:c.989G>A	NP_001369293.1:p.Arg330His
NM_001382448.1:c.1517G>A	NP_001369377.1:p.Arg506His
NM_178443.3:c.1529G>A	NP_848537.1:p.Arg510His