Canonical Allele Identifier: CA6069276

Gene: FERMT3

Linked Data

• ClinVar Variation Id: 1540416
• ClinVar RCV Id: RCV002171988
• dbSNP Id: rs112045200
• ExAC: 11:63990598 C / T
• gnomAD v2: 11-63990598-C-T
• gnomAD v3: 11-64223126-C-T
• gnomAD v4: 11-64223126-C-T
• COSMIC: COSM5512800 ; COSM5512801
• MyVariant Identifiers: chr11:g.63990598C>T (hg19) ; chr11:g.64223126C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223126C>T , CM000673.2:g.64223126C>T	GRCh38
NC_000011.9:g.63990598C>T , CM000673.1:g.63990598C>T	GRCh37
NC_000011.8:g.63747174C>T	NCBI36
NG_016360.1:g.21447C>T , LRG_180:g.21447C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1761C>T	ENSP00000279227.5:p.Asp587=
ENST00000540554.2:n.3273C>T
ENST00000541252.2:c.1209C>T	ENSP00000438885.2:p.Asp403=
ENST00000544997.6:c.1749C>T	ENSP00000445778.2:p.Asp583=
ENST00000545896.2:c.313C>T	ENSP00000440209.2:p.Arg105Cys
ENST00000546255.2:n.2053C>T
ENST00000698845.1:c.*944C>T	ENSP00000513981.1:n.*944C>T
ENST00000698846.1:n.1995C>T
ENST00000698847.1:c.*1154C>T	ENSP00000513982.1:n.*1154C>T
ENST00000698850.1:n.3770C>T
ENST00000698852.1:c.1749C>T	ENSP00000513984.1:p.Asp583=
ENST00000698853.1:c.*978C>T	ENSP00000513985.1:n.*978C>T
ENST00000698854.1:c.*1079C>T	ENSP00000513986.1:n.*1079C>T
ENST00000698855.1:n.3401C>T
ENST00000698856.1:n.3095C>T
ENST00000698859.1:n.2259C>T
ENST00000698860.1:c.1761C>T	ENSP00000513988.1:p.Asp587=
ENST00000698861.1:c.1749C>T	ENSP00000513989.1:p.Asp583=
ENST00000698862.1:c.*1045C>T	ENSP00000513990.1:n.*1045C>T
ENST00000698863.1:c.1749C>T	ENSP00000513991.1:p.Asp583=
ENST00000698864.1:n.2310C>T
ENST00000698865.1:c.1770C>T	ENSP00000513992.1:p.Asp590=
ENST00000698866.1:c.*1537C>T	ENSP00000513993.1:n.*1537C>T
ENST00000698867.1:n.5724C>T
ENST00000698868.1:c.1614C>T	ENSP00000513994.1:p.Asp538=
ENST00000698869.1:c.1515C>T	ENSP00000513995.1:p.Asp505=
ENST00000698870.1:c.1749C>T	ENSP00000513996.1:p.Asp583=
ENST00000698871.1:n.2272C>T
ENST00000698872.1:c.*538C>T	ENSP00000513997.1:n.*538C>T
ENST00000698873.1:c.*944C>T	ENSP00000513998.1:n.*944C>T
ENST00000698874.1:c.1209C>T	ENSP00000513999.1:p.Asp403=
ENST00000698875.1:n.1609C>T
ENST00000698876.1:n.1797C>T
ENST00000698877.1:n.1317C>T
ENST00000698878.1:c.1743C>T	ENSP00000514000.1:p.Asp581=
ENST00000698880.1:c.1617C>T
ENST00000345728.10:c.1749C>T MANE Select	ENSP00000339950.5:p.Asp583=
ENST00000279227.9:c.1761C>T	ENSP00000279227.5:p.Asp587=
ENST00000345728.9:c.1749C>T	ENSP00000339950.5:p.Asp583=
ENST00000545896.1:c.312C>T	ENSP00000440209.1:p.Asp104=
NM_031471.5:c.1749C>T	NP_113659.3:p.Asp583=
NM_178443.2:c.1761C>T , LRG_180t1:c.1761C>T	NP_848537.1:p.Asp587=
XM_011545294.1:c.1761C>T	XP_011543596.1:p.Asp587=
XM_011545295.1:c.1221C>T	XP_011543597.1:p.Asp407=
XM_011545296.1:c.1221C>T	XP_011543598.1:p.Asp407=
XM_011545294.3:c.1761C>T	XP_011543596.1:p.Asp587=
XM_011545295.2:c.1221C>T	XP_011543597.1:p.Asp407=
XM_017018398.2:c.1749C>T	XP_016873887.1:p.Asp583=
XM_017018399.1:c.1209C>T	XP_016873888.1:p.Asp403=
NM_031471.6:c.1749C>T MANE Select	NP_113659.3:p.Asp583=
NM_001382361.1:c.1749C>T	NP_001369290.1:p.Asp583=
NM_001382362.1:c.1761C>T	NP_001369291.1:p.Asp587=
NM_001382363.1:c.1209C>T	NP_001369292.1:p.Asp403=
NM_001382364.1:c.1221C>T	NP_001369293.1:p.Asp407=
NM_001382448.1:c.1749C>T	NP_001369377.1:p.Asp583=
NM_178443.3:c.1761C>T	NP_848537.1:p.Asp587=