Canonical Allele Identifier: CA6069171

Gene: FERMT3

Linked Data

• ClinVar Variation Id: 726538
• ClinVar RCV Id: RCV001476439
• dbSNP Id: rs200660798
• ExAC: 11:63988060 C / T
• gnomAD v2: 11-63988060-C-T
• gnomAD v3: 11-64220588-C-T
• gnomAD v4: 11-64220588-C-T
• MyVariant Identifiers: chr11:g.63988060C>T (hg19) ; chr11:g.64220588C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220588C>T , CM000673.2:g.64220588C>T	GRCh38
NC_000011.9:g.63988060C>T , CM000673.1:g.63988060C>T	GRCh37
NC_000011.8:g.63744636C>T	NCBI36
NG_016360.1:g.18909C>T , LRG_180:g.18909C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1476C>T	ENSP00000279227.5:p.His492=
ENST00000540554.2:n.2642C>T
ENST00000541252.2:c.924C>T	ENSP00000438885.2:p.His308=
ENST00000541326.6:n.885C>T
ENST00000544997.6:c.1464C>T	ENSP00000445778.2:p.His488=
ENST00000545896.2:c.153C>T	ENSP00000440209.2:p.His51=
ENST00000546255.2:n.1768C>T
ENST00000698845.1:c.*659C>T	ENSP00000513981.1:n.*659C>T
ENST00000698846.1:n.1710C>T
ENST00000698847.1:c.*869C>T	ENSP00000513982.1:n.*869C>T
ENST00000698849.1:n.584C>T
ENST00000698850.1:n.1232C>T
ENST00000698852.1:c.1464C>T	ENSP00000513984.1:p.His488=
ENST00000698853.1:c.*693C>T	ENSP00000513985.1:n.*693C>T
ENST00000698854.1:c.*794C>T	ENSP00000513986.1:n.*794C>T
ENST00000698855.1:n.3116C>T
ENST00000698856.1:n.2810C>T
ENST00000698859.1:n.1628C>T
ENST00000698860.1:c.1476C>T	ENSP00000513988.1:p.His492=
ENST00000698861.1:c.1464C>T	ENSP00000513989.1:p.His488=
ENST00000698862.1:c.*760C>T	ENSP00000513990.1:n.*760C>T
ENST00000698863.1:c.1464C>T	ENSP00000513991.1:p.His488=
ENST00000698864.1:n.1679C>T
ENST00000698865.1:c.1485C>T	ENSP00000513992.1:p.His495=
ENST00000698866.1:c.*978C>T	ENSP00000513993.1:n.*978C>T
ENST00000698867.1:n.5439C>T
ENST00000698868.1:c.1329C>T	ENSP00000513994.1:p.His443=
ENST00000698869.1:c.1311+262C>T	ENSP00000513995.1:n.1311+262C>T
ENST00000698870.1:c.1464C>T	ENSP00000513996.1:p.His488=
ENST00000698871.1:n.1987C>T
ENST00000698872.1:c.*253C>T	ENSP00000513997.1:n.*253C>T
ENST00000698873.1:c.*659C>T	ENSP00000513998.1:n.*659C>T
ENST00000698874.1:c.924C>T	ENSP00000513999.1:p.His308=
ENST00000698875.1:n.1324C>T
ENST00000698876.1:n.1512C>T
ENST00000698877.1:n.1032C>T
ENST00000698878.1:c.1458C>T	ENSP00000514000.1:p.His486=
ENST00000698880.1:c.1332C>T
ENST00000345728.10:c.1464C>T MANE Select	ENSP00000339950.5:p.His488=
ENST00000279227.9:c.1476C>T	ENSP00000279227.5:p.His492=
ENST00000345728.9:c.1464C>T	ENSP00000339950.5:p.His488=
ENST00000541326.5:n.880C>T
ENST00000545896.1:c.152C>T	ENSP00000440209.1:p.Thr51Met
NM_031471.5:c.1464C>T	NP_113659.3:p.His488=
NM_178443.2:c.1476C>T , LRG_180t1:c.1476C>T	NP_848537.1:p.His492=
XM_011545294.1:c.1476C>T	XP_011543596.1:p.His492=
XM_011545295.1:c.936C>T	XP_011543597.1:p.His312=
XM_011545296.1:c.936C>T	XP_011543598.1:p.His312=
XM_011545294.3:c.1476C>T	XP_011543596.1:p.His492=
XM_011545295.2:c.936C>T	XP_011543597.1:p.His312=
XM_017018398.2:c.1464C>T	XP_016873887.1:p.His488=
XM_017018399.1:c.924C>T	XP_016873888.1:p.His308=
NM_031471.6:c.1464C>T MANE Select	NP_113659.3:p.His488=
NM_001382361.1:c.1464C>T	NP_001369290.1:p.His488=
NM_001382362.1:c.1476C>T	NP_001369291.1:p.His492=
NM_001382363.1:c.924C>T	NP_001369292.1:p.His308=
NM_001382364.1:c.936C>T	NP_001369293.1:p.His312=
NM_001382448.1:c.1464C>T	NP_001369377.1:p.His488=
NM_178443.3:c.1476C>T	NP_848537.1:p.His492=