Canonical Allele Identifier: CA381087464

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987940C>A (hg19) ; chr11:g.64220468C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220468C>A , CM000673.2:g.64220468C>A	GRCh38
NC_000011.9:g.63987940C>A , CM000673.1:g.63987940C>A	GRCh37
NC_000011.8:g.63744516C>A	NCBI36
NG_016360.1:g.18789C>A , LRG_180:g.18789C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1356C>A	ENSP00000279227.5:p.Cys452Ter
ENST00000540554.2:n.2522C>A
ENST00000541252.2:c.804C>A	ENSP00000438885.2:p.Cys268Ter
ENST00000541326.6:n.765C>A
ENST00000544997.6:c.1344C>A	ENSP00000445778.2:p.Cys448Ter
ENST00000545896.2:c.33C>A	ENSP00000440209.2:p.Cys11Ter
ENST00000546255.2:n.1648C>A
ENST00000698845.1:c.*539C>A	ENSP00000513981.1:n.*539C>A
ENST00000698846.1:n.1590C>A
ENST00000698847.1:c.*749C>A	ENSP00000513982.1:n.*749C>A
ENST00000698848.1:n.642C>A
ENST00000698849.1:n.464C>A
ENST00000698850.1:n.1112C>A
ENST00000698852.1:c.1344C>A	ENSP00000513984.1:p.Cys448Ter
ENST00000698853.1:c.*573C>A	ENSP00000513985.1:n.*573C>A
ENST00000698854.1:c.*674C>A	ENSP00000513986.1:n.*674C>A
ENST00000698855.1:n.2996C>A
ENST00000698856.1:n.2690C>A
ENST00000698859.1:n.1508C>A
ENST00000698860.1:c.1356C>A	ENSP00000513988.1:p.Cys452Ter
ENST00000698861.1:c.1344C>A	ENSP00000513989.1:p.Cys448Ter
ENST00000698862.1:c.*640C>A	ENSP00000513990.1:n.*640C>A
ENST00000698863.1:c.1344C>A	ENSP00000513991.1:p.Cys448Ter
ENST00000698864.1:n.1559C>A
ENST00000698865.1:c.1365C>A	ENSP00000513992.1:p.Cys455Ter
ENST00000698866.1:c.*858C>A	ENSP00000513993.1:n.*858C>A
ENST00000698867.1:n.5319C>A
ENST00000698868.1:c.1209C>A	ENSP00000513994.1:p.Cys403Ter
ENST00000698869.1:c.1311+142C>A	ENSP00000513995.1:n.1311+142C>A
ENST00000698870.1:c.1344C>A	ENSP00000513996.1:p.Cys448Ter
ENST00000698871.1:n.1867C>A
ENST00000698872.1:c.*133C>A	ENSP00000513997.1:n.*133C>A
ENST00000698873.1:c.*539C>A	ENSP00000513998.1:n.*539C>A
ENST00000698874.1:c.804C>A	ENSP00000513999.1:p.Cys268Ter
ENST00000698875.1:n.1204C>A
ENST00000698876.1:n.1392C>A
ENST00000698877.1:n.912C>A
ENST00000698878.1:c.1338C>A	ENSP00000514000.1:p.Cys446Ter
ENST00000698880.1:c.1212C>A
ENST00000345728.10:c.1344C>A MANE Select	ENSP00000339950.5:p.Cys448Ter
ENST00000279227.9:c.1356C>A	ENSP00000279227.5:p.Cys452Ter
ENST00000345728.9:c.1344C>A	ENSP00000339950.5:p.Cys448Ter
ENST00000541326.5:n.760C>A
ENST00000545896.1:c.32C>A	ENSP00000440209.1:p.Ala11Asp
NM_031471.5:c.1344C>A	NP_113659.3:p.Cys448Ter
NM_178443.2:c.1356C>A , LRG_180t1:c.1356C>A	NP_848537.1:p.Cys452Ter
XM_011545294.1:c.1356C>A	XP_011543596.1:p.Cys452Ter
XM_011545295.1:c.816C>A	XP_011543597.1:p.Cys272Ter
XM_011545296.1:c.816C>A	XP_011543598.1:p.Cys272Ter
XM_011545294.3:c.1356C>A	XP_011543596.1:p.Cys452Ter
XM_011545295.2:c.816C>A	XP_011543597.1:p.Cys272Ter
XM_017018398.2:c.1344C>A	XP_016873887.1:p.Cys448Ter
XM_017018399.1:c.804C>A	XP_016873888.1:p.Cys268Ter
NM_031471.6:c.1344C>A MANE Select	NP_113659.3:p.Cys448Ter
NM_001382361.1:c.1344C>A	NP_001369290.1:p.Cys448Ter
NM_001382362.1:c.1356C>A	NP_001369291.1:p.Cys452Ter
NM_001382363.1:c.804C>A	NP_001369292.1:p.Cys268Ter
NM_001382364.1:c.816C>A	NP_001369293.1:p.Cys272Ter
NM_001382448.1:c.1344C>A	NP_001369377.1:p.Cys448Ter
NM_178443.3:c.1356C>A	NP_848537.1:p.Cys452Ter