Canonical Allele Identifier: CA1978642826
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64223090C= , CM000673.2:g.64223090C= GRCh38
NC_000011.9:g.63990562C= , CM000673.1:g.63990562C= GRCh37
NC_000011.8:g.63747138C= NCBI36
NG_016360.1:g.21411C= , LRG_180:g.21411C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1725C= ENSP00000279227.5:p.Asn575=
ENST00000540554.2:n.3237C=
ENST00000541252.2:c.1173C= ENSP00000438885.2:p.Asn391=
ENST00000544997.6:c.1713C= ENSP00000445778.2:p.Asn571=
ENST00000545896.2:c.277C= ENSP00000440209.2:p.Gln93=
ENST00000546255.2:n.2017C=
ENST00000698845.1:c.*908C= ENSP00000513981.1:n.*908C=
ENST00000698846.1:n.1959C=
ENST00000698847.1:c.*1118C= ENSP00000513982.1:n.*1118C=
ENST00000698850.1:n.3734C=
ENST00000698852.1:c.1713C= ENSP00000513984.1:p.Asn571=
ENST00000698853.1:c.*942C= ENSP00000513985.1:n.*942C=
ENST00000698854.1:c.*1043C= ENSP00000513986.1:n.*1043C=
ENST00000698855.1:n.3365C=
ENST00000698856.1:n.3059C=
ENST00000698859.1:n.2223C=
ENST00000698860.1:c.1725C= ENSP00000513988.1:p.Asn575=
ENST00000698861.1:c.1713C= ENSP00000513989.1:p.Asn571=
ENST00000698862.1:c.*1009C= ENSP00000513990.1:n.*1009C=
ENST00000698863.1:c.1713C= ENSP00000513991.1:p.Asn571=
ENST00000698864.1:n.2274C=
ENST00000698865.1:c.1734C= ENSP00000513992.1:p.Asn578=
ENST00000698866.1:c.*1501C= ENSP00000513993.1:n.*1501C=
ENST00000698867.1:n.5688C=
ENST00000698868.1:c.1578C= ENSP00000513994.1:p.Asn526=
ENST00000698869.1:c.1479C= ENSP00000513995.1:p.Asn493=
ENST00000698870.1:c.1713C= ENSP00000513996.1:p.Asn571=
ENST00000698871.1:n.2236C=
ENST00000698872.1:c.*502C= ENSP00000513997.1:n.*502C=
ENST00000698873.1:c.*908C= ENSP00000513998.1:n.*908C=
ENST00000698874.1:c.1173C= ENSP00000513999.1:p.Asn391=
ENST00000698875.1:n.1573C=
ENST00000698876.1:n.1761C=
ENST00000698877.1:n.1281C=
ENST00000698878.1:c.1707C= ENSP00000514000.1:p.Asn569=
ENST00000698880.1:c.1581C=
ENST00000345728.10:c.1713C= MANE Select ENSP00000339950.5:p.Asn571=
ENST00000279227.9:c.1725C= ENSP00000279227.5:p.Asn575=
ENST00000345728.9:c.1713C= ENSP00000339950.5:p.Asn571=
ENST00000540554.1:n.349C=
ENST00000545896.1:c.276C= ENSP00000440209.1:p.Asn92=
NM_031471.5:c.1713C= NP_113659.3:p.Asn571=
NM_178443.2:c.1725C= , LRG_180t1:c.1725C= NP_848537.1:p.Asn575=
XM_011545294.1:c.1725C= XP_011543596.1:p.Asn575=
XM_011545295.1:c.1185C= XP_011543597.1:p.Asn395=
XM_011545296.1:c.1185C= XP_011543598.1:p.Asn395=
XM_011545294.3:c.1725C= XP_011543596.1:p.Asn575=
XM_011545295.2:c.1185C= XP_011543597.1:p.Asn395=
XM_017018398.2:c.1713C= XP_016873887.1:p.Asn571=
XM_017018399.1:c.1173C= XP_016873888.1:p.Asn391=
NM_031471.6:c.1713C= MANE Select NP_113659.3:p.Asn571=
NM_001382361.1:c.1713C= NP_001369290.1:p.Asn571=
NM_001382362.1:c.1725C= NP_001369291.1:p.Asn575=
NM_001382363.1:c.1173C= NP_001369292.1:p.Asn391=
NM_001382364.1:c.1185C= NP_001369293.1:p.Asn395=
NM_001382448.1:c.1713C= NP_001369377.1:p.Asn571=
NM_178443.3:c.1725C= NP_848537.1:p.Asn575=