Canonical Allele Identifier: CA381086979

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987711T>G (hg19) ; chr11:g.64220239T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220239T>G , CM000673.2:g.64220239T>G	GRCh38
NC_000011.9:g.63987711T>G , CM000673.1:g.63987711T>G	GRCh37
NC_000011.8:g.63744287T>G	NCBI36
NG_016360.1:g.18560T>G , LRG_180:g.18560T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1236T>G	ENSP00000279227.5:p.Asp412Glu
ENST00000540554.2:n.2293T>G
ENST00000541252.2:c.684T>G	ENSP00000438885.2:p.Asp228Glu
ENST00000541326.6:n.536T>G
ENST00000544997.6:c.1224T>G	ENSP00000445778.2:p.Asp408Glu
ENST00000546255.2:n.1419T>G
ENST00000698845.1:c.*419T>G	ENSP00000513981.1:n.*419T>G
ENST00000698846.1:n.1361T>G
ENST00000698847.1:c.*629T>G	ENSP00000513982.1:n.*629T>G
ENST00000698848.1:n.413T>G
ENST00000698849.1:n.344T>G
ENST00000698850.1:n.883T>G
ENST00000698852.1:c.1224T>G	ENSP00000513984.1:p.Asp408Glu
ENST00000698853.1:c.*453T>G	ENSP00000513985.1:n.*453T>G
ENST00000698854.1:c.*554T>G	ENSP00000513986.1:n.*554T>G
ENST00000698855.1:n.2876T>G
ENST00000698856.1:n.2461T>G
ENST00000698859.1:n.1388T>G
ENST00000698860.1:c.1236T>G	ENSP00000513988.1:p.Asp412Glu
ENST00000698861.1:c.1224T>G	ENSP00000513989.1:p.Asp408Glu
ENST00000698862.1:c.*520T>G	ENSP00000513990.1:n.*520T>G
ENST00000698863.1:c.1224T>G	ENSP00000513991.1:p.Asp408Glu
ENST00000698864.1:n.1330T>G
ENST00000698865.1:c.1245T>G	ENSP00000513992.1:p.Asp415Glu
ENST00000698866.1:c.*629T>G	ENSP00000513993.1:n.*629T>G
ENST00000698867.1:n.5199T>G
ENST00000698868.1:c.1089T>G	ENSP00000513994.1:p.Asp363Glu
ENST00000698869.1:c.1224T>G	ENSP00000513995.1:p.Asp408Glu
ENST00000698870.1:c.1224T>G	ENSP00000513996.1:p.Asp408Glu
ENST00000698871.1:n.1747T>G
ENST00000698872.1:c.*13T>G	ENSP00000513997.1:n.*13T>G
ENST00000698873.1:c.*419T>G	ENSP00000513998.1:n.*419T>G
ENST00000698874.1:c.684T>G	ENSP00000513999.1:p.Asp228Glu
ENST00000698875.1:n.1084T>G
ENST00000698876.1:n.1163T>G
ENST00000698877.1:n.792T>G
ENST00000698878.1:c.1224T>G	ENSP00000514000.1:p.Asp408Glu
ENST00000698880.1:c.1064T>G
ENST00000345728.10:c.1224T>G MANE Select	ENSP00000339950.5:p.Asp408Glu
ENST00000279227.9:c.1236T>G	ENSP00000279227.5:p.Asp412Glu
ENST00000345728.9:c.1224T>G	ENSP00000339950.5:p.Asp408Glu
ENST00000540957.1:n.377T>G
ENST00000541326.5:n.531T>G
NM_031471.5:c.1224T>G	NP_113659.3:p.Asp408Glu
NM_178443.2:c.1236T>G , LRG_180t1:c.1236T>G	NP_848537.1:p.Asp412Glu
XM_011545294.1:c.1236T>G	XP_011543596.1:p.Asp412Glu
XM_011545295.1:c.696T>G	XP_011543597.1:p.Asp232Glu
XM_011545296.1:c.696T>G	XP_011543598.1:p.Asp232Glu
XM_011545294.3:c.1236T>G	XP_011543596.1:p.Asp412Glu
XM_011545295.2:c.696T>G	XP_011543597.1:p.Asp232Glu
XM_017018398.2:c.1224T>G	XP_016873887.1:p.Asp408Glu
XM_017018399.1:c.684T>G	XP_016873888.1:p.Asp228Glu
NM_031471.6:c.1224T>G MANE Select	NP_113659.3:p.Asp408Glu
NM_001382361.1:c.1224T>G	NP_001369290.1:p.Asp408Glu
NM_001382362.1:c.1236T>G	NP_001369291.1:p.Asp412Glu
NM_001382363.1:c.684T>G	NP_001369292.1:p.Asp228Glu
NM_001382364.1:c.696T>G	NP_001369293.1:p.Asp232Glu
NM_001382448.1:c.1224T>G	NP_001369377.1:p.Asp408Glu
NM_178443.3:c.1236T>G	NP_848537.1:p.Asp412Glu