Canonical Allele Identifier: CA1978642795
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64223084C= , CM000673.2:g.64223084C= GRCh38
NC_000011.9:g.63990556C= , CM000673.1:g.63990556C= GRCh37
NC_000011.8:g.63747132C= NCBI36
NG_016360.1:g.21405C= , LRG_180:g.21405C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1719C= ENSP00000279227.5:p.Ile573=
ENST00000540554.2:n.3231C=
ENST00000541252.2:c.1167C= ENSP00000438885.2:p.Ile389=
ENST00000544997.6:c.1707C= ENSP00000445778.2:p.Ile569=
ENST00000545896.2:c.271C= ENSP00000440209.2:p.Arg91=
ENST00000546255.2:n.2011C=
ENST00000698845.1:c.*902C= ENSP00000513981.1:n.*902C=
ENST00000698846.1:n.1953C=
ENST00000698847.1:c.*1112C= ENSP00000513982.1:n.*1112C=
ENST00000698850.1:n.3728C=
ENST00000698852.1:c.1707C= ENSP00000513984.1:p.Ile569=
ENST00000698853.1:c.*936C= ENSP00000513985.1:n.*936C=
ENST00000698854.1:c.*1037C= ENSP00000513986.1:n.*1037C=
ENST00000698855.1:n.3359C=
ENST00000698856.1:n.3053C=
ENST00000698859.1:n.2217C=
ENST00000698860.1:c.1719C= ENSP00000513988.1:p.Ile573=
ENST00000698861.1:c.1707C= ENSP00000513989.1:p.Ile569=
ENST00000698862.1:c.*1003C= ENSP00000513990.1:n.*1003C=
ENST00000698863.1:c.1707C= ENSP00000513991.1:p.Ile569=
ENST00000698864.1:n.2268C=
ENST00000698865.1:c.1728C= ENSP00000513992.1:p.Ile576=
ENST00000698866.1:c.*1495C= ENSP00000513993.1:n.*1495C=
ENST00000698867.1:n.5682C=
ENST00000698868.1:c.1572C= ENSP00000513994.1:p.Ile524=
ENST00000698869.1:c.1473C= ENSP00000513995.1:p.Ile491=
ENST00000698870.1:c.1707C= ENSP00000513996.1:p.Ile569=
ENST00000698871.1:n.2230C=
ENST00000698872.1:c.*496C= ENSP00000513997.1:n.*496C=
ENST00000698873.1:c.*902C= ENSP00000513998.1:n.*902C=
ENST00000698874.1:c.1167C= ENSP00000513999.1:p.Ile389=
ENST00000698875.1:n.1567C=
ENST00000698876.1:n.1755C=
ENST00000698877.1:n.1275C=
ENST00000698878.1:c.1701C= ENSP00000514000.1:p.Ile567=
ENST00000698880.1:c.1575C=
ENST00000345728.10:c.1707C= MANE Select ENSP00000339950.5:p.Ile569=
ENST00000279227.9:c.1719C= ENSP00000279227.5:p.Ile573=
ENST00000345728.9:c.1707C= ENSP00000339950.5:p.Ile569=
ENST00000540554.1:n.343C=
ENST00000545896.1:c.270C= ENSP00000440209.1:p.Ile90=
NM_031471.5:c.1707C= NP_113659.3:p.Ile569=
NM_178443.2:c.1719C= , LRG_180t1:c.1719C= NP_848537.1:p.Ile573=
XM_011545294.1:c.1719C= XP_011543596.1:p.Ile573=
XM_011545295.1:c.1179C= XP_011543597.1:p.Ile393=
XM_011545296.1:c.1179C= XP_011543598.1:p.Ile393=
XM_011545294.3:c.1719C= XP_011543596.1:p.Ile573=
XM_011545295.2:c.1179C= XP_011543597.1:p.Ile393=
XM_017018398.2:c.1707C= XP_016873887.1:p.Ile569=
XM_017018399.1:c.1167C= XP_016873888.1:p.Ile389=
NM_031471.6:c.1707C= MANE Select NP_113659.3:p.Ile569=
NM_001382361.1:c.1707C= NP_001369290.1:p.Ile569=
NM_001382362.1:c.1719C= NP_001369291.1:p.Ile573=
NM_001382363.1:c.1167C= NP_001369292.1:p.Ile389=
NM_001382364.1:c.1179C= NP_001369293.1:p.Ile393=
NM_001382448.1:c.1707C= NP_001369377.1:p.Ile569=
NM_178443.3:c.1719C= NP_848537.1:p.Ile573=