Canonical Allele Identifier: CA475151753

Gene: FERMT3

Linked Data

• dbSNP Id: rs1946751427
• gnomAD v4: 11-64223054-G-A
• MyVariant Identifiers: chr11:g.63990526G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223054G>A , CM000673.2:g.64223054G>A	GRCh38
NC_000011.9:g.63990526G>A , CM000673.1:g.63990526G>A	GRCh37
NC_000011.8:g.63747102G>A	NCBI36
NG_016360.1:g.21375G>A , LRG_180:g.21375G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1689G>A	ENSP00000279227.5:p.Lys563=
ENST00000540554.2:n.3201G>A
ENST00000541252.2:c.1137G>A	ENSP00000438885.2:p.Lys379=
ENST00000544997.6:c.1677G>A	ENSP00000445778.2:p.Lys559=
ENST00000545896.2:c.241G>A	ENSP00000440209.2:p.Gly81Arg
ENST00000546255.2:n.1981G>A
ENST00000698845.1:c.*872G>A	ENSP00000513981.1:n.*872G>A
ENST00000698846.1:n.1923G>A
ENST00000698847.1:c.*1082G>A	ENSP00000513982.1:n.*1082G>A
ENST00000698850.1:n.3698G>A
ENST00000698852.1:c.1677G>A	ENSP00000513984.1:p.Lys559=
ENST00000698853.1:c.*906G>A	ENSP00000513985.1:n.*906G>A
ENST00000698854.1:c.*1007G>A	ENSP00000513986.1:n.*1007G>A
ENST00000698855.1:n.3329G>A
ENST00000698856.1:n.3023G>A
ENST00000698859.1:n.2187G>A
ENST00000698860.1:c.1689G>A	ENSP00000513988.1:p.Lys563=
ENST00000698861.1:c.1677G>A	ENSP00000513989.1:p.Lys559=
ENST00000698862.1:c.*973G>A	ENSP00000513990.1:n.*973G>A
ENST00000698863.1:c.1677G>A	ENSP00000513991.1:p.Lys559=
ENST00000698864.1:n.2238G>A
ENST00000698865.1:c.1698G>A	ENSP00000513992.1:p.Lys566=
ENST00000698866.1:c.*1465G>A	ENSP00000513993.1:n.*1465G>A
ENST00000698867.1:n.5652G>A
ENST00000698868.1:c.1542G>A	ENSP00000513994.1:p.Lys514=
ENST00000698869.1:c.1443G>A	ENSP00000513995.1:p.Lys481=
ENST00000698870.1:c.1677G>A	ENSP00000513996.1:p.Lys559=
ENST00000698871.1:n.2200G>A
ENST00000698872.1:c.*466G>A	ENSP00000513997.1:n.*466G>A
ENST00000698873.1:c.*872G>A	ENSP00000513998.1:n.*872G>A
ENST00000698874.1:c.1137G>A	ENSP00000513999.1:p.Lys379=
ENST00000698875.1:n.1537G>A
ENST00000698876.1:n.1725G>A
ENST00000698877.1:n.1245G>A
ENST00000698878.1:c.1671G>A	ENSP00000514000.1:p.Lys557=
ENST00000698880.1:c.1545G>A
ENST00000345728.10:c.1677G>A MANE Select	ENSP00000339950.5:p.Lys559=
ENST00000279227.9:c.1689G>A	ENSP00000279227.5:p.Lys563=
ENST00000345728.9:c.1677G>A	ENSP00000339950.5:p.Lys559=
ENST00000540554.1:n.313G>A
ENST00000545896.1:c.240G>A	ENSP00000440209.1:p.Lys80=
NM_031471.5:c.1677G>A	NP_113659.3:p.Lys559=
NM_178443.2:c.1689G>A , LRG_180t1:c.1689G>A	NP_848537.1:p.Lys563=
XM_011545294.1:c.1689G>A	XP_011543596.1:p.Lys563=
XM_011545295.1:c.1149G>A	XP_011543597.1:p.Lys383=
XM_011545296.1:c.1149G>A	XP_011543598.1:p.Lys383=
XM_011545294.3:c.1689G>A	XP_011543596.1:p.Lys563=
XM_011545295.2:c.1149G>A	XP_011543597.1:p.Lys383=
XM_017018398.2:c.1677G>A	XP_016873887.1:p.Lys559=
XM_017018399.1:c.1137G>A	XP_016873888.1:p.Lys379=
NM_031471.6:c.1677G>A MANE Select	NP_113659.3:p.Lys559=
NM_001382361.1:c.1677G>A	NP_001369290.1:p.Lys559=
NM_001382362.1:c.1689G>A	NP_001369291.1:p.Lys563=
NM_001382363.1:c.1137G>A	NP_001369292.1:p.Lys379=
NM_001382364.1:c.1149G>A	NP_001369293.1:p.Lys383=
NM_001382448.1:c.1677G>A	NP_001369377.1:p.Lys559=
NM_178443.3:c.1689G>A	NP_848537.1:p.Lys563=