Canonical Allele Identifier: CA1978638747
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64220397A= , CM000673.2:g.64220397A= GRCh38
NC_000011.9:g.63987869A= , CM000673.1:g.63987869A= GRCh37
NC_000011.8:g.63744445A= NCBI36
NG_016360.1:g.18718A= , LRG_180:g.18718A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1324-39A= ENSP00000279227.5:n.1324-39A=
ENST00000540554.2:n.2451A=
ENST00000541252.2:c.772-39A= ENSP00000438885.2:n.772-39A=
ENST00000541326.6:n.694A=
ENST00000544997.6:c.1312-39A= ENSP00000445778.2:n.1312-39A=
ENST00000546255.2:n.1577A=
ENST00000698845.1:c.*507-39A= ENSP00000513981.1:n.*507-39A=
ENST00000698846.1:n.1519A=
ENST00000698847.1:c.*717-39A= ENSP00000513982.1:n.*717-39A=
ENST00000698848.1:n.571A=
ENST00000698849.1:n.432-39A=
ENST00000698850.1:n.1041A=
ENST00000698852.1:c.1312-39A= ENSP00000513984.1:n.1312-39A=
ENST00000698853.1:c.*541-39A= ENSP00000513985.1:n.*541-39A=
ENST00000698854.1:c.*642-39A= ENSP00000513986.1:n.*642-39A=
ENST00000698855.1:n.2964-39A=
ENST00000698856.1:n.2619A=
ENST00000698859.1:n.1476-39A=
ENST00000698860.1:c.1324-39A= ENSP00000513988.1:n.1324-39A=
ENST00000698861.1:c.1312-39A= ENSP00000513989.1:n.1312-39A=
ENST00000698862.1:c.*608-39A= ENSP00000513990.1:n.*608-39A=
ENST00000698863.1:c.1312-39A= ENSP00000513991.1:n.1312-39A=
ENST00000698864.1:n.1488A=
ENST00000698865.1:c.1333-39A= ENSP00000513992.1:n.1333-39A=
ENST00000698866.1:c.*787A= ENSP00000513993.1:n.*787A=
ENST00000698867.1:n.5287-39A=
ENST00000698868.1:c.1177-39A= ENSP00000513994.1:n.1177-39A=
ENST00000698869.1:c.1311+71A= ENSP00000513995.1:n.1311+71A=
ENST00000698870.1:c.1312-39A= ENSP00000513996.1:n.1312-39A=
ENST00000698871.1:n.1835-39A=
ENST00000698872.1:c.*101-39A= ENSP00000513997.1:n.*101-39A=
ENST00000698873.1:c.*507-39A= ENSP00000513998.1:n.*507-39A=
ENST00000698874.1:c.772-39A= ENSP00000513999.1:n.772-39A=
ENST00000698875.1:n.1172-39A=
ENST00000698876.1:n.1321A=
ENST00000698877.1:n.880-39A=
ENST00000698878.1:c.1312-45A= ENSP00000514000.1:n.1312-45A=
ENST00000698880.1:c.1152-11A=
ENST00000345728.10:c.1312-39A= MANE Select ENSP00000339950.5:n.1312-39A=
ENST00000279227.9:c.1324-39A= ENSP00000279227.5:n.1324-39A=
ENST00000345728.9:c.1312-39A= ENSP00000339950.5:n.1312-39A=
ENST00000540957.1:n.535A=
ENST00000541326.5:n.689A=
NM_031471.5:c.1312-39A= NP_113659.3:n.1312-39A=
NM_178443.2:c.1324-39A= , LRG_180t1:c.1324-39A= NP_848537.1:n.1324-39A=
XM_011545294.1:c.1324-39A= XP_011543596.1:n.1324-39A=
XM_011545295.1:c.784-39A= XP_011543597.1:n.784-39A=
XM_011545296.1:c.784-39A= XP_011543598.1:n.784-39A=
XM_011545294.3:c.1324-39A= XP_011543596.1:n.1324-39A=
XM_011545295.2:c.784-39A= XP_011543597.1:n.784-39A=
XM_017018398.2:c.1312-39A= XP_016873887.1:n.1312-39A=
XM_017018399.1:c.772-39A= XP_016873888.1:n.772-39A=
NM_031471.6:c.1312-39A= MANE Select NP_113659.3:n.1312-39A=
NM_001382361.1:c.1312-39A= NP_001369290.1:n.1312-39A=
NM_001382362.1:c.1324-39A= NP_001369291.1:n.1324-39A=
NM_001382363.1:c.772-39A= NP_001369292.1:n.772-39A=
NM_001382364.1:c.784-39A= NP_001369293.1:n.784-39A=
NM_001382448.1:c.1312-39A= NP_001369377.1:n.1312-39A=
NM_178443.3:c.1324-39A= NP_848537.1:n.1324-39A=