Canonical Allele Identifier: CA381087684

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987998G>A (hg19) ; chr11:g.64220526G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220526G>A , CM000673.2:g.64220526G>A	GRCh38
NC_000011.9:g.63987998G>A , CM000673.1:g.63987998G>A	GRCh37
NC_000011.8:g.63744574G>A	NCBI36
NG_016360.1:g.18847G>A , LRG_180:g.18847G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1414G>A	ENSP00000279227.5:p.Ala472Thr
ENST00000540554.2:n.2580G>A
ENST00000541252.2:c.862G>A	ENSP00000438885.2:p.Ala288Thr
ENST00000541326.6:n.823G>A
ENST00000544997.6:c.1402G>A	ENSP00000445778.2:p.Ala468Thr
ENST00000545896.2:c.91G>A	ENSP00000440209.2:p.Ala31Thr
ENST00000546255.2:n.1706G>A
ENST00000698845.1:c.*597G>A	ENSP00000513981.1:n.*597G>A
ENST00000698846.1:n.1648G>A
ENST00000698847.1:c.*807G>A	ENSP00000513982.1:n.*807G>A
ENST00000698849.1:n.522G>A
ENST00000698850.1:n.1170G>A
ENST00000698852.1:c.1402G>A	ENSP00000513984.1:p.Ala468Thr
ENST00000698853.1:c.*631G>A	ENSP00000513985.1:n.*631G>A
ENST00000698854.1:c.*732G>A	ENSP00000513986.1:n.*732G>A
ENST00000698855.1:n.3054G>A
ENST00000698856.1:n.2748G>A
ENST00000698859.1:n.1566G>A
ENST00000698860.1:c.1414G>A	ENSP00000513988.1:p.Ala472Thr
ENST00000698861.1:c.1402G>A	ENSP00000513989.1:p.Ala468Thr
ENST00000698862.1:c.*698G>A	ENSP00000513990.1:n.*698G>A
ENST00000698863.1:c.1402G>A	ENSP00000513991.1:p.Ala468Thr
ENST00000698864.1:n.1617G>A
ENST00000698865.1:c.1423G>A	ENSP00000513992.1:p.Ala475Thr
ENST00000698866.1:c.*916G>A	ENSP00000513993.1:n.*916G>A
ENST00000698867.1:n.5377G>A
ENST00000698868.1:c.1267G>A	ENSP00000513994.1:p.Ala423Thr
ENST00000698869.1:c.1311+200G>A	ENSP00000513995.1:n.1311+200G>A
ENST00000698870.1:c.1402G>A	ENSP00000513996.1:p.Ala468Thr
ENST00000698871.1:n.1925G>A
ENST00000698872.1:c.*191G>A	ENSP00000513997.1:n.*191G>A
ENST00000698873.1:c.*597G>A	ENSP00000513998.1:n.*597G>A
ENST00000698874.1:c.862G>A	ENSP00000513999.1:p.Ala288Thr
ENST00000698875.1:n.1262G>A
ENST00000698876.1:n.1450G>A
ENST00000698877.1:n.970G>A
ENST00000698878.1:c.1396G>A	ENSP00000514000.1:p.Ala466Thr
ENST00000698880.1:c.1270G>A
ENST00000345728.10:c.1402G>A MANE Select	ENSP00000339950.5:p.Ala468Thr
ENST00000279227.9:c.1414G>A	ENSP00000279227.5:p.Ala472Thr
ENST00000345728.9:c.1402G>A	ENSP00000339950.5:p.Ala468Thr
ENST00000541326.5:n.818G>A
ENST00000545896.1:c.90G>A	ENSP00000440209.1:p.Arg30=
NM_031471.5:c.1402G>A	NP_113659.3:p.Ala468Thr
NM_178443.2:c.1414G>A , LRG_180t1:c.1414G>A	NP_848537.1:p.Ala472Thr
XM_011545294.1:c.1414G>A	XP_011543596.1:p.Ala472Thr
XM_011545295.1:c.874G>A	XP_011543597.1:p.Ala292Thr
XM_011545296.1:c.874G>A	XP_011543598.1:p.Ala292Thr
XM_011545294.3:c.1414G>A	XP_011543596.1:p.Ala472Thr
XM_011545295.2:c.874G>A	XP_011543597.1:p.Ala292Thr
XM_017018398.2:c.1402G>A	XP_016873887.1:p.Ala468Thr
XM_017018399.1:c.862G>A	XP_016873888.1:p.Ala288Thr
NM_031471.6:c.1402G>A MANE Select	NP_113659.3:p.Ala468Thr
NM_001382361.1:c.1402G>A	NP_001369290.1:p.Ala468Thr
NM_001382362.1:c.1414G>A	NP_001369291.1:p.Ala472Thr
NM_001382363.1:c.862G>A	NP_001369292.1:p.Ala288Thr
NM_001382364.1:c.874G>A	NP_001369293.1:p.Ala292Thr
NM_001382448.1:c.1402G>A	NP_001369377.1:p.Ala468Thr
NM_178443.3:c.1414G>A	NP_848537.1:p.Ala472Thr