Canonical Allele Identifier: CA381089848

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990600T>G (hg19) ; chr11:g.64223128T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223128T>G , CM000673.2:g.64223128T>G	GRCh38
NC_000011.9:g.63990600T>G , CM000673.1:g.63990600T>G	GRCh37
NC_000011.8:g.63747176T>G	NCBI36
NG_016360.1:g.21449T>G , LRG_180:g.21449T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1763T>G	ENSP00000279227.5:p.Val588Gly
ENST00000540554.2:n.3275T>G
ENST00000541252.2:c.1211T>G	ENSP00000438885.2:p.Val404Gly
ENST00000544997.6:c.1751T>G	ENSP00000445778.2:p.Val584Gly
ENST00000545896.2:c.315T>G	ENSP00000440209.2:p.Arg105=
ENST00000546255.2:n.2055T>G
ENST00000698845.1:c.*946T>G	ENSP00000513981.1:n.*946T>G
ENST00000698846.1:n.1997T>G
ENST00000698847.1:c.*1156T>G	ENSP00000513982.1:n.*1156T>G
ENST00000698850.1:n.3772T>G
ENST00000698852.1:c.1751T>G	ENSP00000513984.1:p.Val584Gly
ENST00000698853.1:c.*980T>G	ENSP00000513985.1:n.*980T>G
ENST00000698854.1:c.*1081T>G	ENSP00000513986.1:n.*1081T>G
ENST00000698855.1:n.3403T>G
ENST00000698856.1:n.3097T>G
ENST00000698859.1:n.2261T>G
ENST00000698860.1:c.1763T>G	ENSP00000513988.1:p.Val588Gly
ENST00000698861.1:c.1751T>G	ENSP00000513989.1:p.Val584Gly
ENST00000698862.1:c.*1047T>G	ENSP00000513990.1:n.*1047T>G
ENST00000698863.1:c.1751T>G	ENSP00000513991.1:p.Val584Gly
ENST00000698864.1:n.2312T>G
ENST00000698865.1:c.1772T>G	ENSP00000513992.1:p.Val591Gly
ENST00000698866.1:c.*1539T>G	ENSP00000513993.1:n.*1539T>G
ENST00000698867.1:n.5726T>G
ENST00000698868.1:c.1616T>G	ENSP00000513994.1:p.Val539Gly
ENST00000698869.1:c.1517T>G	ENSP00000513995.1:p.Val506Gly
ENST00000698870.1:c.1751T>G	ENSP00000513996.1:p.Val584Gly
ENST00000698871.1:n.2274T>G
ENST00000698872.1:c.*540T>G	ENSP00000513997.1:n.*540T>G
ENST00000698873.1:c.*946T>G	ENSP00000513998.1:n.*946T>G
ENST00000698874.1:c.1211T>G	ENSP00000513999.1:p.Val404Gly
ENST00000698875.1:n.1611T>G
ENST00000698876.1:n.1799T>G
ENST00000698877.1:n.1319T>G
ENST00000698878.1:c.1745T>G	ENSP00000514000.1:p.Val582Gly
ENST00000698880.1:c.1619T>G
ENST00000345728.10:c.1751T>G MANE Select	ENSP00000339950.5:p.Val584Gly
ENST00000279227.9:c.1763T>G	ENSP00000279227.5:p.Val588Gly
ENST00000345728.9:c.1751T>G	ENSP00000339950.5:p.Val584Gly
ENST00000545896.1:c.314T>G	ENSP00000440209.1:p.Val105Gly
NM_031471.5:c.1751T>G	NP_113659.3:p.Val584Gly
NM_178443.2:c.1763T>G , LRG_180t1:c.1763T>G	NP_848537.1:p.Val588Gly
XM_011545294.1:c.1763T>G	XP_011543596.1:p.Val588Gly
XM_011545295.1:c.1223T>G	XP_011543597.1:p.Val408Gly
XM_011545296.1:c.1223T>G	XP_011543598.1:p.Val408Gly
XM_011545294.3:c.1763T>G	XP_011543596.1:p.Val588Gly
XM_011545295.2:c.1223T>G	XP_011543597.1:p.Val408Gly
XM_017018398.2:c.1751T>G	XP_016873887.1:p.Val584Gly
XM_017018399.1:c.1211T>G	XP_016873888.1:p.Val404Gly
NM_031471.6:c.1751T>G MANE Select	NP_113659.3:p.Val584Gly
NM_001382361.1:c.1751T>G	NP_001369290.1:p.Val584Gly
NM_001382362.1:c.1763T>G	NP_001369291.1:p.Val588Gly
NM_001382363.1:c.1211T>G	NP_001369292.1:p.Val404Gly
NM_001382364.1:c.1223T>G	NP_001369293.1:p.Val408Gly
NM_001382448.1:c.1751T>G	NP_001369377.1:p.Val584Gly
NM_178443.3:c.1763T>G	NP_848537.1:p.Val588Gly