Canonical Allele Identifier: CA381086977

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987710A>T (hg19) ; chr11:g.64220238A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220238A>T , CM000673.2:g.64220238A>T	GRCh38
NC_000011.9:g.63987710A>T , CM000673.1:g.63987710A>T	GRCh37
NC_000011.8:g.63744286A>T	NCBI36
NG_016360.1:g.18559A>T , LRG_180:g.18559A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1235A>T	ENSP00000279227.5:p.Asp412Val
ENST00000540554.2:n.2292A>T
ENST00000541252.2:c.683A>T	ENSP00000438885.2:p.Asp228Val
ENST00000541326.6:n.535A>T
ENST00000544997.6:c.1223A>T	ENSP00000445778.2:p.Asp408Val
ENST00000546255.2:n.1418A>T
ENST00000698845.1:c.*418A>T	ENSP00000513981.1:n.*418A>T
ENST00000698846.1:n.1360A>T
ENST00000698847.1:c.*628A>T	ENSP00000513982.1:n.*628A>T
ENST00000698848.1:n.412A>T
ENST00000698849.1:n.343A>T
ENST00000698850.1:n.882A>T
ENST00000698852.1:c.1223A>T	ENSP00000513984.1:p.Asp408Val
ENST00000698853.1:c.*452A>T	ENSP00000513985.1:n.*452A>T
ENST00000698854.1:c.*553A>T	ENSP00000513986.1:n.*553A>T
ENST00000698855.1:n.2875A>T
ENST00000698856.1:n.2460A>T
ENST00000698859.1:n.1387A>T
ENST00000698860.1:c.1235A>T	ENSP00000513988.1:p.Asp412Val
ENST00000698861.1:c.1223A>T	ENSP00000513989.1:p.Asp408Val
ENST00000698862.1:c.*519A>T	ENSP00000513990.1:n.*519A>T
ENST00000698863.1:c.1223A>T	ENSP00000513991.1:p.Asp408Val
ENST00000698864.1:n.1329A>T
ENST00000698865.1:c.1244A>T	ENSP00000513992.1:p.Asp415Val
ENST00000698866.1:c.*628A>T	ENSP00000513993.1:n.*628A>T
ENST00000698867.1:n.5198A>T
ENST00000698868.1:c.1088A>T	ENSP00000513994.1:p.Asp363Val
ENST00000698869.1:c.1223A>T	ENSP00000513995.1:p.Asp408Val
ENST00000698870.1:c.1223A>T	ENSP00000513996.1:p.Asp408Val
ENST00000698871.1:n.1746A>T
ENST00000698872.1:c.*12A>T	ENSP00000513997.1:n.*12A>T
ENST00000698873.1:c.*418A>T	ENSP00000513998.1:n.*418A>T
ENST00000698874.1:c.683A>T	ENSP00000513999.1:p.Asp228Val
ENST00000698875.1:n.1083A>T
ENST00000698876.1:n.1162A>T
ENST00000698877.1:n.791A>T
ENST00000698878.1:c.1223A>T	ENSP00000514000.1:p.Asp408Val
ENST00000698880.1:c.1063A>T
ENST00000345728.10:c.1223A>T MANE Select	ENSP00000339950.5:p.Asp408Val
ENST00000279227.9:c.1235A>T	ENSP00000279227.5:p.Asp412Val
ENST00000345728.9:c.1223A>T	ENSP00000339950.5:p.Asp408Val
ENST00000540957.1:n.376A>T
ENST00000541326.5:n.530A>T
NM_031471.5:c.1223A>T	NP_113659.3:p.Asp408Val
NM_178443.2:c.1235A>T , LRG_180t1:c.1235A>T	NP_848537.1:p.Asp412Val
XM_011545294.1:c.1235A>T	XP_011543596.1:p.Asp412Val
XM_011545295.1:c.695A>T	XP_011543597.1:p.Asp232Val
XM_011545296.1:c.695A>T	XP_011543598.1:p.Asp232Val
XM_011545294.3:c.1235A>T	XP_011543596.1:p.Asp412Val
XM_011545295.2:c.695A>T	XP_011543597.1:p.Asp232Val
XM_017018398.2:c.1223A>T	XP_016873887.1:p.Asp408Val
XM_017018399.1:c.683A>T	XP_016873888.1:p.Asp228Val
NM_031471.6:c.1223A>T MANE Select	NP_113659.3:p.Asp408Val
NM_001382361.1:c.1223A>T	NP_001369290.1:p.Asp408Val
NM_001382362.1:c.1235A>T	NP_001369291.1:p.Asp412Val
NM_001382363.1:c.683A>T	NP_001369292.1:p.Asp228Val
NM_001382364.1:c.695A>T	NP_001369293.1:p.Asp232Val
NM_001382448.1:c.1223A>T	NP_001369377.1:p.Asp408Val
NM_178443.3:c.1235A>T	NP_848537.1:p.Asp412Val