Canonical Allele Identifier: CA381087540

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987957G>T (hg19) ; chr11:g.64220485G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220485G>T , CM000673.2:g.64220485G>T	GRCh38
NC_000011.9:g.63987957G>T , CM000673.1:g.63987957G>T	GRCh37
NC_000011.8:g.63744533G>T	NCBI36
NG_016360.1:g.18806G>T , LRG_180:g.18806G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1373G>T	ENSP00000279227.5:p.Gly458Val
ENST00000540554.2:n.2539G>T
ENST00000541252.2:c.821G>T	ENSP00000438885.2:p.Gly274Val
ENST00000541326.6:n.782G>T
ENST00000544997.6:c.1361G>T	ENSP00000445778.2:p.Gly454Val
ENST00000545896.2:c.50G>T	ENSP00000440209.2:p.Gly17Val
ENST00000546255.2:n.1665G>T
ENST00000698845.1:c.*556G>T	ENSP00000513981.1:n.*556G>T
ENST00000698846.1:n.1607G>T
ENST00000698847.1:c.*766G>T	ENSP00000513982.1:n.*766G>T
ENST00000698849.1:n.481G>T
ENST00000698850.1:n.1129G>T
ENST00000698852.1:c.1361G>T	ENSP00000513984.1:p.Gly454Val
ENST00000698853.1:c.*590G>T	ENSP00000513985.1:n.*590G>T
ENST00000698854.1:c.*691G>T	ENSP00000513986.1:n.*691G>T
ENST00000698855.1:n.3013G>T
ENST00000698856.1:n.2707G>T
ENST00000698859.1:n.1525G>T
ENST00000698860.1:c.1373G>T	ENSP00000513988.1:p.Gly458Val
ENST00000698861.1:c.1361G>T	ENSP00000513989.1:p.Gly454Val
ENST00000698862.1:c.*657G>T	ENSP00000513990.1:n.*657G>T
ENST00000698863.1:c.1361G>T	ENSP00000513991.1:p.Gly454Val
ENST00000698864.1:n.1576G>T
ENST00000698865.1:c.1382G>T	ENSP00000513992.1:p.Gly461Val
ENST00000698866.1:c.*875G>T	ENSP00000513993.1:n.*875G>T
ENST00000698867.1:n.5336G>T
ENST00000698868.1:c.1226G>T	ENSP00000513994.1:p.Gly409Val
ENST00000698869.1:c.1311+159G>T	ENSP00000513995.1:n.1311+159G>T
ENST00000698870.1:c.1361G>T	ENSP00000513996.1:p.Gly454Val
ENST00000698871.1:n.1884G>T
ENST00000698872.1:c.*150G>T	ENSP00000513997.1:n.*150G>T
ENST00000698873.1:c.*556G>T	ENSP00000513998.1:n.*556G>T
ENST00000698874.1:c.821G>T	ENSP00000513999.1:p.Gly274Val
ENST00000698875.1:n.1221G>T
ENST00000698876.1:n.1409G>T
ENST00000698877.1:n.929G>T
ENST00000698878.1:c.1355G>T	ENSP00000514000.1:p.Gly452Val
ENST00000698880.1:c.1229G>T
ENST00000345728.10:c.1361G>T MANE Select	ENSP00000339950.5:p.Gly454Val
ENST00000279227.9:c.1373G>T	ENSP00000279227.5:p.Gly458Val
ENST00000345728.9:c.1361G>T	ENSP00000339950.5:p.Gly454Val
ENST00000541326.5:n.777G>T
ENST00000545896.1:c.49G>T	ENSP00000440209.1:p.Ala17Ser
NM_031471.5:c.1361G>T	NP_113659.3:p.Gly454Val
NM_178443.2:c.1373G>T , LRG_180t1:c.1373G>T	NP_848537.1:p.Gly458Val
XM_011545294.1:c.1373G>T	XP_011543596.1:p.Gly458Val
XM_011545295.1:c.833G>T	XP_011543597.1:p.Gly278Val
XM_011545296.1:c.833G>T	XP_011543598.1:p.Gly278Val
XM_011545294.3:c.1373G>T	XP_011543596.1:p.Gly458Val
XM_011545295.2:c.833G>T	XP_011543597.1:p.Gly278Val
XM_017018398.2:c.1361G>T	XP_016873887.1:p.Gly454Val
XM_017018399.1:c.821G>T	XP_016873888.1:p.Gly274Val
NM_031471.6:c.1361G>T MANE Select	NP_113659.3:p.Gly454Val
NM_001382361.1:c.1361G>T	NP_001369290.1:p.Gly454Val
NM_001382362.1:c.1373G>T	NP_001369291.1:p.Gly458Val
NM_001382363.1:c.821G>T	NP_001369292.1:p.Gly274Val
NM_001382364.1:c.833G>T	NP_001369293.1:p.Gly278Val
NM_001382448.1:c.1361G>T	NP_001369377.1:p.Gly454Val
NM_178443.3:c.1373G>T	NP_848537.1:p.Gly458Val