Canonical Allele Identifier: CA1978642961
Gene: FERMT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64223152A= , CM000673.2:g.64223152A= GRCh38
NC_000011.9:g.63990624A= , CM000673.1:g.63990624A= GRCh37
NC_000011.8:g.63747200A= NCBI36
NG_016360.1:g.21473A= , LRG_180:g.21473A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1787A= ENSP00000279227.5:p.Asn596=
ENST00000540554.2:n.3299A=
ENST00000541252.2:c.1235A= ENSP00000438885.2:p.Asn412=
ENST00000544997.6:c.1775A= ENSP00000445778.2:p.Asn592=
ENST00000545896.2:c.339A= ENSP00000440209.2:p.Gln113=
ENST00000546255.2:n.2079A=
ENST00000698845.1:c.*970A= ENSP00000513981.1:n.*970A=
ENST00000698846.1:n.2021A=
ENST00000698847.1:c.*1180A= ENSP00000513982.1:n.*1180A=
ENST00000698850.1:n.3796A=
ENST00000698852.1:c.1775A= ENSP00000513984.1:p.Asn592=
ENST00000698853.1:c.*1004A= ENSP00000513985.1:n.*1004A=
ENST00000698854.1:c.*1105A= ENSP00000513986.1:n.*1105A=
ENST00000698855.1:n.3427A=
ENST00000698856.1:n.3121A=
ENST00000698859.1:n.2285A=
ENST00000698860.1:c.1787A= ENSP00000513988.1:p.Asn596=
ENST00000698861.1:c.1775A= ENSP00000513989.1:p.Asn592=
ENST00000698862.1:c.*1071A= ENSP00000513990.1:n.*1071A=
ENST00000698863.1:c.1775A= ENSP00000513991.1:p.Asn592=
ENST00000698864.1:n.2336A=
ENST00000698865.1:c.1796A= ENSP00000513992.1:p.Asn599=
ENST00000698866.1:c.*1563A= ENSP00000513993.1:n.*1563A=
ENST00000698867.1:n.5750A=
ENST00000698868.1:c.1640A= ENSP00000513994.1:p.Asn547=
ENST00000698869.1:c.1541A= ENSP00000513995.1:p.Asn514=
ENST00000698870.1:c.1775A= ENSP00000513996.1:p.Asn592=
ENST00000698871.1:n.2298A=
ENST00000698872.1:c.*564A= ENSP00000513997.1:n.*564A=
ENST00000698873.1:c.*970A= ENSP00000513998.1:n.*970A=
ENST00000698874.1:c.1235A= ENSP00000513999.1:p.Asn412=
ENST00000698875.1:n.1635A=
ENST00000698876.1:n.1823A=
ENST00000698877.1:n.1343A=
ENST00000698878.1:c.1769A= ENSP00000514000.1:p.Asn590=
ENST00000698880.1:c.1643A=
ENST00000345728.10:c.1775A= MANE Select ENSP00000339950.5:p.Asn592=
ENST00000279227.9:c.1787A= ENSP00000279227.5:p.Asn596=
ENST00000345728.9:c.1775A= ENSP00000339950.5:p.Asn592=
ENST00000545896.1:c.338A= ENSP00000440209.1:p.Asn113=
NM_031471.5:c.1775A= NP_113659.3:p.Asn592=
NM_178443.2:c.1787A= , LRG_180t1:c.1787A= NP_848537.1:p.Asn596=
XM_011545294.1:c.1787A= XP_011543596.1:p.Asn596=
XM_011545295.1:c.1247A= XP_011543597.1:p.Asn416=
XM_011545296.1:c.1247A= XP_011543598.1:p.Asn416=
XM_011545294.3:c.1787A= XP_011543596.1:p.Asn596=
XM_011545295.2:c.1247A= XP_011543597.1:p.Asn416=
XM_017018398.2:c.1775A= XP_016873887.1:p.Asn592=
XM_017018399.1:c.1235A= XP_016873888.1:p.Asn412=
NM_031471.6:c.1775A= MANE Select NP_113659.3:p.Asn592=
NM_001382361.1:c.1775A= NP_001369290.1:p.Asn592=
NM_001382362.1:c.1787A= NP_001369291.1:p.Asn596=
NM_001382363.1:c.1235A= NP_001369292.1:p.Asn412=
NM_001382364.1:c.1247A= NP_001369293.1:p.Asn416=
NM_001382448.1:c.1775A= NP_001369377.1:p.Asn592=
NM_178443.3:c.1787A= NP_848537.1:p.Asn596=