Canonical Allele Identifier: CA6069095

Gene: FERMT3

Linked Data

• ClinVar Variation Id: 1027172
• ClinVar RCV Id: RCV001327731
• dbSNP Id: rs748029046
• ExAC: 11:63987726 C / T
• gnomAD v2: 11-63987726-C-T
• gnomAD v3: 11-64220254-C-T
• gnomAD v4: 11-64220254-C-T
• MyVariant Identifiers: chr11:g.63987726C>T (hg19) ; chr11:g.64220254C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220254C>T , CM000673.2:g.64220254C>T	GRCh38
NC_000011.9:g.63987726C>T , CM000673.1:g.63987726C>T	GRCh37
NC_000011.8:g.63744302C>T	NCBI36
NG_016360.1:g.18575C>T , LRG_180:g.18575C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1251C>T	ENSP00000279227.5:p.Gly417=
ENST00000540554.2:n.2308C>T
ENST00000541252.2:c.699C>T	ENSP00000438885.2:p.Gly233=
ENST00000541326.6:n.551C>T
ENST00000544997.6:c.1239C>T	ENSP00000445778.2:p.Gly413=
ENST00000546255.2:n.1434C>T
ENST00000698845.1:c.*434C>T	ENSP00000513981.1:n.*434C>T
ENST00000698846.1:n.1376C>T
ENST00000698847.1:c.*644C>T	ENSP00000513982.1:n.*644C>T
ENST00000698848.1:n.428C>T
ENST00000698849.1:n.359C>T
ENST00000698850.1:n.898C>T
ENST00000698852.1:c.1239C>T	ENSP00000513984.1:p.Gly413=
ENST00000698853.1:c.*468C>T	ENSP00000513985.1:n.*468C>T
ENST00000698854.1:c.*569C>T	ENSP00000513986.1:n.*569C>T
ENST00000698855.1:n.2891C>T
ENST00000698856.1:n.2476C>T
ENST00000698859.1:n.1403C>T
ENST00000698860.1:c.1251C>T	ENSP00000513988.1:p.Gly417=
ENST00000698861.1:c.1239C>T	ENSP00000513989.1:p.Gly413=
ENST00000698862.1:c.*535C>T	ENSP00000513990.1:n.*535C>T
ENST00000698863.1:c.1239C>T	ENSP00000513991.1:p.Gly413=
ENST00000698864.1:n.1345C>T
ENST00000698865.1:c.1260C>T	ENSP00000513992.1:p.Gly420=
ENST00000698866.1:c.*644C>T	ENSP00000513993.1:n.*644C>T
ENST00000698867.1:n.5214C>T
ENST00000698868.1:c.1104C>T	ENSP00000513994.1:p.Gly368=
ENST00000698869.1:c.1239C>T	ENSP00000513995.1:p.Gly413=
ENST00000698870.1:c.1239C>T	ENSP00000513996.1:p.Gly413=
ENST00000698871.1:n.1762C>T
ENST00000698872.1:c.*28C>T	ENSP00000513997.1:n.*28C>T
ENST00000698873.1:c.*434C>T	ENSP00000513998.1:n.*434C>T
ENST00000698874.1:c.699C>T	ENSP00000513999.1:p.Gly233=
ENST00000698875.1:n.1099C>T
ENST00000698876.1:n.1178C>T
ENST00000698877.1:n.807C>T
ENST00000698878.1:c.1239C>T	ENSP00000514000.1:p.Gly413=
ENST00000698880.1:c.1079C>T
ENST00000345728.10:c.1239C>T MANE Select	ENSP00000339950.5:p.Gly413=
ENST00000279227.9:c.1251C>T	ENSP00000279227.5:p.Gly417=
ENST00000345728.9:c.1239C>T	ENSP00000339950.5:p.Gly413=
ENST00000540957.1:n.392C>T
ENST00000541326.5:n.546C>T
NM_031471.5:c.1239C>T	NP_113659.3:p.Gly413=
NM_178443.2:c.1251C>T , LRG_180t1:c.1251C>T	NP_848537.1:p.Gly417=
XM_011545294.1:c.1251C>T	XP_011543596.1:p.Gly417=
XM_011545295.1:c.711C>T	XP_011543597.1:p.Gly237=
XM_011545296.1:c.711C>T	XP_011543598.1:p.Gly237=
XM_011545294.3:c.1251C>T	XP_011543596.1:p.Gly417=
XM_011545295.2:c.711C>T	XP_011543597.1:p.Gly237=
XM_017018398.2:c.1239C>T	XP_016873887.1:p.Gly413=
XM_017018399.1:c.699C>T	XP_016873888.1:p.Gly233=
NM_031471.6:c.1239C>T MANE Select	NP_113659.3:p.Gly413=
NM_001382361.1:c.1239C>T	NP_001369290.1:p.Gly413=
NM_001382362.1:c.1251C>T	NP_001369291.1:p.Gly417=
NM_001382363.1:c.699C>T	NP_001369292.1:p.Gly233=
NM_001382364.1:c.711C>T	NP_001369293.1:p.Gly237=
NM_001382448.1:c.1239C>T	NP_001369377.1:p.Gly413=
NM_178443.3:c.1251C>T	NP_848537.1:p.Gly417=