Canonical Allele Identifier: CA1978639278
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220654G= , CM000673.2:g.64220654G= GRCh38
NC_000011.9:g.63988126G= , CM000673.1:g.63988126G= GRCh37
NC_000011.8:g.63744702G= NCBI36
NG_016360.1:g.18975G= , LRG_180:g.18975G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1542G= ENSP00000279227.5:p.Lys514=
ENST00000540554.2:n.2708G=
ENST00000541252.2:c.990G= ENSP00000438885.2:p.Lys330=
ENST00000541326.6:n.951G=
ENST00000544997.6:c.1530G= ENSP00000445778.2:p.Lys510=
ENST00000545896.2:c.219G= ENSP00000440209.2:p.Lys73=
ENST00000546255.2:n.1834G=
ENST00000698845.1:c.*725G= ENSP00000513981.1:n.*725G=
ENST00000698846.1:n.1776G=
ENST00000698847.1:c.*935G= ENSP00000513982.1:n.*935G=
ENST00000698849.1:n.650G=
ENST00000698850.1:n.1298G=
ENST00000698852.1:c.1530G= ENSP00000513984.1:p.Lys510=
ENST00000698853.1:c.*759G= ENSP00000513985.1:n.*759G=
ENST00000698854.1:c.*860G= ENSP00000513986.1:n.*860G=
ENST00000698855.1:n.3182G=
ENST00000698856.1:n.2876G=
ENST00000698859.1:n.1694G=
ENST00000698860.1:c.1542G= ENSP00000513988.1:p.Lys514=
ENST00000698861.1:c.1530G= ENSP00000513989.1:p.Lys510=
ENST00000698862.1:c.*826G= ENSP00000513990.1:n.*826G=
ENST00000698863.1:c.1530G= ENSP00000513991.1:p.Lys510=
ENST00000698864.1:n.1745G=
ENST00000698865.1:c.1551G= ENSP00000513992.1:p.Lys517=
ENST00000698866.1:c.*1044G= ENSP00000513993.1:n.*1044G=
ENST00000698867.1:n.5505G=
ENST00000698868.1:c.1395G= ENSP00000513994.1:p.Lys465=
ENST00000698869.1:c.1311+328G= ENSP00000513995.1:n.1311+328G=
ENST00000698870.1:c.1530G= ENSP00000513996.1:p.Lys510=
ENST00000698871.1:n.2053G=
ENST00000698872.1:c.*319G= ENSP00000513997.1:n.*319G=
ENST00000698873.1:c.*725G= ENSP00000513998.1:n.*725G=
ENST00000698874.1:c.990G= ENSP00000513999.1:p.Lys330=
ENST00000698875.1:n.1390G=
ENST00000698876.1:n.1578G=
ENST00000698877.1:n.1098G=
ENST00000698878.1:c.1524G= ENSP00000514000.1:p.Lys508=
ENST00000698880.1:c.1398G=
ENST00000345728.10:c.1530G= MANE Select ENSP00000339950.5:p.Lys510=
ENST00000279227.9:c.1542G= ENSP00000279227.5:p.Lys514=
ENST00000345728.9:c.1530G= ENSP00000339950.5:p.Lys510=
ENST00000545896.1:c.218G= ENSP00000440209.1:p.Ser73=
NM_031471.5:c.1530G= NP_113659.3:p.Lys510=
NM_178443.2:c.1542G= , LRG_180t1:c.1542G= NP_848537.1:p.Lys514=
XM_011545294.1:c.1542G= XP_011543596.1:p.Lys514=
XM_011545295.1:c.1002G= XP_011543597.1:p.Lys334=
XM_011545296.1:c.1002G= XP_011543598.1:p.Lys334=
XM_011545294.3:c.1542G= XP_011543596.1:p.Lys514=
XM_011545295.2:c.1002G= XP_011543597.1:p.Lys334=
XM_017018398.2:c.1530G= XP_016873887.1:p.Lys510=
XM_017018399.1:c.990G= XP_016873888.1:p.Lys330=
NM_031471.6:c.1530G= MANE Select NP_113659.3:p.Lys510=
NM_001382361.1:c.1530G= NP_001369290.1:p.Lys510=
NM_001382362.1:c.1542G= NP_001369291.1:p.Lys514=
NM_001382363.1:c.990G= NP_001369292.1:p.Lys330=
NM_001382364.1:c.1002G= NP_001369293.1:p.Lys334=
NM_001382448.1:c.1530G= NP_001369377.1:p.Lys510=
NM_178443.3:c.1542G= NP_848537.1:p.Lys514=