Canonical Allele Identifier: CA381087607

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987982C>G (hg19) ; chr11:g.64220510C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220510C>G , CM000673.2:g.64220510C>G	GRCh38
NC_000011.9:g.63987982C>G , CM000673.1:g.63987982C>G	GRCh37
NC_000011.8:g.63744558C>G	NCBI36
NG_016360.1:g.18831C>G , LRG_180:g.18831C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1398C>G	ENSP00000279227.5:p.Tyr466Ter
ENST00000540554.2:n.2564C>G
ENST00000541252.2:c.846C>G	ENSP00000438885.2:p.Tyr282Ter
ENST00000541326.6:n.807C>G
ENST00000544997.6:c.1386C>G	ENSP00000445778.2:p.Tyr462Ter
ENST00000545896.2:c.75C>G	ENSP00000440209.2:p.Tyr25Ter
ENST00000546255.2:n.1690C>G
ENST00000698845.1:c.*581C>G	ENSP00000513981.1:n.*581C>G
ENST00000698846.1:n.1632C>G
ENST00000698847.1:c.*791C>G	ENSP00000513982.1:n.*791C>G
ENST00000698849.1:n.506C>G
ENST00000698850.1:n.1154C>G
ENST00000698852.1:c.1386C>G	ENSP00000513984.1:p.Tyr462Ter
ENST00000698853.1:c.*615C>G	ENSP00000513985.1:n.*615C>G
ENST00000698854.1:c.*716C>G	ENSP00000513986.1:n.*716C>G
ENST00000698855.1:n.3038C>G
ENST00000698856.1:n.2732C>G
ENST00000698859.1:n.1550C>G
ENST00000698860.1:c.1398C>G	ENSP00000513988.1:p.Tyr466Ter
ENST00000698861.1:c.1386C>G	ENSP00000513989.1:p.Tyr462Ter
ENST00000698862.1:c.*682C>G	ENSP00000513990.1:n.*682C>G
ENST00000698863.1:c.1386C>G	ENSP00000513991.1:p.Tyr462Ter
ENST00000698864.1:n.1601C>G
ENST00000698865.1:c.1407C>G	ENSP00000513992.1:p.Tyr469Ter
ENST00000698866.1:c.*900C>G	ENSP00000513993.1:n.*900C>G
ENST00000698867.1:n.5361C>G
ENST00000698868.1:c.1251C>G	ENSP00000513994.1:p.Tyr417Ter
ENST00000698869.1:c.1311+184C>G	ENSP00000513995.1:n.1311+184C>G
ENST00000698870.1:c.1386C>G	ENSP00000513996.1:p.Tyr462Ter
ENST00000698871.1:n.1909C>G
ENST00000698872.1:c.*175C>G	ENSP00000513997.1:n.*175C>G
ENST00000698873.1:c.*581C>G	ENSP00000513998.1:n.*581C>G
ENST00000698874.1:c.846C>G	ENSP00000513999.1:p.Tyr282Ter
ENST00000698875.1:n.1246C>G
ENST00000698876.1:n.1434C>G
ENST00000698877.1:n.954C>G
ENST00000698878.1:c.1380C>G	ENSP00000514000.1:p.Tyr460Ter
ENST00000698880.1:c.1254C>G
ENST00000345728.10:c.1386C>G MANE Select	ENSP00000339950.5:p.Tyr462Ter
ENST00000279227.9:c.1398C>G	ENSP00000279227.5:p.Tyr466Ter
ENST00000345728.9:c.1386C>G	ENSP00000339950.5:p.Tyr462Ter
ENST00000541326.5:n.802C>G
ENST00000545896.1:c.74C>G	ENSP00000440209.1:p.Thr25Arg
NM_031471.5:c.1386C>G	NP_113659.3:p.Tyr462Ter
NM_178443.2:c.1398C>G , LRG_180t1:c.1398C>G	NP_848537.1:p.Tyr466Ter
XM_011545294.1:c.1398C>G	XP_011543596.1:p.Tyr466Ter
XM_011545295.1:c.858C>G	XP_011543597.1:p.Tyr286Ter
XM_011545296.1:c.858C>G	XP_011543598.1:p.Tyr286Ter
XM_011545294.3:c.1398C>G	XP_011543596.1:p.Tyr466Ter
XM_011545295.2:c.858C>G	XP_011543597.1:p.Tyr286Ter
XM_017018398.2:c.1386C>G	XP_016873887.1:p.Tyr462Ter
XM_017018399.1:c.846C>G	XP_016873888.1:p.Tyr282Ter
NM_031471.6:c.1386C>G MANE Select	NP_113659.3:p.Tyr462Ter
NM_001382361.1:c.1386C>G	NP_001369290.1:p.Tyr462Ter
NM_001382362.1:c.1398C>G	NP_001369291.1:p.Tyr466Ter
NM_001382363.1:c.846C>G	NP_001369292.1:p.Tyr282Ter
NM_001382364.1:c.858C>G	NP_001369293.1:p.Tyr286Ter
NM_001382448.1:c.1386C>G	NP_001369377.1:p.Tyr462Ter
NM_178443.3:c.1398C>G	NP_848537.1:p.Tyr466Ter