Canonical Allele Identifier: CA1978642966
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64223158G= , CM000673.2:g.64223158G= GRCh38
NC_000011.9:g.63990630G= , CM000673.1:g.63990630G= GRCh37
NC_000011.8:g.63747206G= NCBI36
NG_016360.1:g.21479G= , LRG_180:g.21479G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1793G= ENSP00000279227.5:p.Arg598=
ENST00000540554.2:n.3305G=
ENST00000541252.2:c.1241G= ENSP00000438885.2:p.Arg414=
ENST00000544997.6:c.1781G= ENSP00000445778.2:p.Arg594=
ENST00000545896.2:c.345G= ENSP00000440209.2:p.Ala115=
ENST00000546255.2:n.2085G=
ENST00000698845.1:c.*976G= ENSP00000513981.1:n.*976G=
ENST00000698846.1:n.2027G=
ENST00000698847.1:c.*1186G= ENSP00000513982.1:n.*1186G=
ENST00000698850.1:n.3802G=
ENST00000698852.1:c.1781G= ENSP00000513984.1:p.Arg594=
ENST00000698853.1:c.*1010G= ENSP00000513985.1:n.*1010G=
ENST00000698854.1:c.*1111G= ENSP00000513986.1:n.*1111G=
ENST00000698855.1:n.3433G=
ENST00000698856.1:n.3127G=
ENST00000698859.1:n.2291G=
ENST00000698860.1:c.1793G= ENSP00000513988.1:p.Arg598=
ENST00000698861.1:c.1781G= ENSP00000513989.1:p.Arg594=
ENST00000698862.1:c.*1077G= ENSP00000513990.1:n.*1077G=
ENST00000698863.1:c.1781G= ENSP00000513991.1:p.Arg594=
ENST00000698864.1:n.2342G=
ENST00000698865.1:c.1802G= ENSP00000513992.1:p.Arg601=
ENST00000698866.1:c.*1569G= ENSP00000513993.1:n.*1569G=
ENST00000698867.1:n.5756G=
ENST00000698868.1:c.1646G= ENSP00000513994.1:p.Arg549=
ENST00000698869.1:c.1547G= ENSP00000513995.1:p.Arg516=
ENST00000698870.1:c.1781G= ENSP00000513996.1:p.Arg594=
ENST00000698871.1:n.2304G=
ENST00000698872.1:c.*570G= ENSP00000513997.1:n.*570G=
ENST00000698873.1:c.*976G= ENSP00000513998.1:n.*976G=
ENST00000698874.1:c.1241G= ENSP00000513999.1:p.Arg414=
ENST00000698875.1:n.1641G=
ENST00000698876.1:n.1829G=
ENST00000698877.1:n.1349G=
ENST00000698878.1:c.1775G= ENSP00000514000.1:p.Arg592=
ENST00000698880.1:c.1649G=
ENST00000345728.10:c.1781G= MANE Select ENSP00000339950.5:p.Arg594=
ENST00000279227.9:c.1793G= ENSP00000279227.5:p.Arg598=
ENST00000345728.9:c.1781G= ENSP00000339950.5:p.Arg594=
ENST00000545896.1:c.344G= ENSP00000440209.1:p.Arg115=
NM_031471.5:c.1781G= NP_113659.3:p.Arg594=
NM_178443.2:c.1793G= , LRG_180t1:c.1793G= NP_848537.1:p.Arg598=
XM_011545294.1:c.1793G= XP_011543596.1:p.Arg598=
XM_011545295.1:c.1253G= XP_011543597.1:p.Arg418=
XM_011545296.1:c.1253G= XP_011543598.1:p.Arg418=
XM_011545294.3:c.1793G= XP_011543596.1:p.Arg598=
XM_011545295.2:c.1253G= XP_011543597.1:p.Arg418=
XM_017018398.2:c.1781G= XP_016873887.1:p.Arg594=
XM_017018399.1:c.1241G= XP_016873888.1:p.Arg414=
NM_031471.6:c.1781G= MANE Select NP_113659.3:p.Arg594=
NM_001382361.1:c.1781G= NP_001369290.1:p.Arg594=
NM_001382362.1:c.1793G= NP_001369291.1:p.Arg598=
NM_001382363.1:c.1241G= NP_001369292.1:p.Arg414=
NM_001382364.1:c.1253G= NP_001369293.1:p.Arg418=
NM_001382448.1:c.1781G= NP_001369377.1:p.Arg594=
NM_178443.3:c.1793G= NP_848537.1:p.Arg598=