Canonical Allele Identifier: CA381087619

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987985C>A (hg19) ; chr11:g.64220513C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220513C>A , CM000673.2:g.64220513C>A	GRCh38
NC_000011.9:g.63987985C>A , CM000673.1:g.63987985C>A	GRCh37
NC_000011.8:g.63744561C>A	NCBI36
NG_016360.1:g.18834C>A , LRG_180:g.18834C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1401C>A	ENSP00000279227.5:p.Thr467=
ENST00000540554.2:n.2567C>A
ENST00000541252.2:c.849C>A	ENSP00000438885.2:p.Thr283=
ENST00000541326.6:n.810C>A
ENST00000544997.6:c.1389C>A	ENSP00000445778.2:p.Thr463=
ENST00000545896.2:c.78C>A	ENSP00000440209.2:p.Thr26=
ENST00000546255.2:n.1693C>A
ENST00000698845.1:c.*584C>A	ENSP00000513981.1:n.*584C>A
ENST00000698846.1:n.1635C>A
ENST00000698847.1:c.*794C>A	ENSP00000513982.1:n.*794C>A
ENST00000698849.1:n.509C>A
ENST00000698850.1:n.1157C>A
ENST00000698852.1:c.1389C>A	ENSP00000513984.1:p.Thr463=
ENST00000698853.1:c.*618C>A	ENSP00000513985.1:n.*618C>A
ENST00000698854.1:c.*719C>A	ENSP00000513986.1:n.*719C>A
ENST00000698855.1:n.3041C>A
ENST00000698856.1:n.2735C>A
ENST00000698859.1:n.1553C>A
ENST00000698860.1:c.1401C>A	ENSP00000513988.1:p.Thr467=
ENST00000698861.1:c.1389C>A	ENSP00000513989.1:p.Thr463=
ENST00000698862.1:c.*685C>A	ENSP00000513990.1:n.*685C>A
ENST00000698863.1:c.1389C>A	ENSP00000513991.1:p.Thr463=
ENST00000698864.1:n.1604C>A
ENST00000698865.1:c.1410C>A	ENSP00000513992.1:p.Thr470=
ENST00000698866.1:c.*903C>A	ENSP00000513993.1:n.*903C>A
ENST00000698867.1:n.5364C>A
ENST00000698868.1:c.1254C>A	ENSP00000513994.1:p.Thr418=
ENST00000698869.1:c.1311+187C>A	ENSP00000513995.1:n.1311+187C>A
ENST00000698870.1:c.1389C>A	ENSP00000513996.1:p.Thr463=
ENST00000698871.1:n.1912C>A
ENST00000698872.1:c.*178C>A	ENSP00000513997.1:n.*178C>A
ENST00000698873.1:c.*584C>A	ENSP00000513998.1:n.*584C>A
ENST00000698874.1:c.849C>A	ENSP00000513999.1:p.Thr283=
ENST00000698875.1:n.1249C>A
ENST00000698876.1:n.1437C>A
ENST00000698877.1:n.957C>A
ENST00000698878.1:c.1383C>A	ENSP00000514000.1:p.Thr461=
ENST00000698880.1:c.1257C>A
ENST00000345728.10:c.1389C>A MANE Select	ENSP00000339950.5:p.Thr463=
ENST00000279227.9:c.1401C>A	ENSP00000279227.5:p.Thr467=
ENST00000345728.9:c.1389C>A	ENSP00000339950.5:p.Thr463=
ENST00000541326.5:n.805C>A
ENST00000545896.1:c.77C>A	ENSP00000440209.1:p.Pro26Gln
NM_031471.5:c.1389C>A	NP_113659.3:p.Thr463=
NM_178443.2:c.1401C>A , LRG_180t1:c.1401C>A	NP_848537.1:p.Thr467=
XM_011545294.1:c.1401C>A	XP_011543596.1:p.Thr467=
XM_011545295.1:c.861C>A	XP_011543597.1:p.Thr287=
XM_011545296.1:c.861C>A	XP_011543598.1:p.Thr287=
XM_011545294.3:c.1401C>A	XP_011543596.1:p.Thr467=
XM_011545295.2:c.861C>A	XP_011543597.1:p.Thr287=
XM_017018398.2:c.1389C>A	XP_016873887.1:p.Thr463=
XM_017018399.1:c.849C>A	XP_016873888.1:p.Thr283=
NM_031471.6:c.1389C>A MANE Select	NP_113659.3:p.Thr463=
NM_001382361.1:c.1389C>A	NP_001369290.1:p.Thr463=
NM_001382362.1:c.1401C>A	NP_001369291.1:p.Thr467=
NM_001382363.1:c.849C>A	NP_001369292.1:p.Thr283=
NM_001382364.1:c.861C>A	NP_001369293.1:p.Thr287=
NM_001382448.1:c.1389C>A	NP_001369377.1:p.Thr463=
NM_178443.3:c.1401C>A	NP_848537.1:p.Thr467=