Canonical Allele Identifier: CA2322607159
Gene: DNM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10786575C= , CM000681.2:g.10786575C= GRCh38
NC_000019.9:g.10897251C= , CM000681.1:g.10897251C= GRCh37
NC_000019.8:g.10758251C= NCBI36
NG_008792.1:g.73497C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682285.1:n.1049C=
ENST00000682524.1:n.1049C=
ENST00000683738.1:n.1049C=
ENST00000355667.11:c.861C= ENSP00000347890.6:p.Asn287=
ENST00000389253.9:c.861C= MANE Select ENSP00000373905.4:p.Asn287=
ENST00000355667.10:c.861C= ENSP00000347890.6:p.Asn287=
ENST00000359692.10:c.861C= ENSP00000352721.6:p.Asn287=
ENST00000389253.8:c.861C= ENSP00000373905.3:p.Asn287=
ENST00000408974.8:c.861C= ENSP00000386192.3:p.Asn287=
ENST00000585892.5:c.861C= ENSP00000468734.1:p.Asn287=
ENST00000586130.1:n.146C=
ENST00000587485.1:n.367C=
ENST00000587830.2:c.117C= ENSP00000466603.2:p.Asn39=
ENST00000591701.5:n.221C=
NM_001005360.2:c.861C= NP_001005360.1:p.Asn287=
NM_001005361.2:c.861C= NP_001005361.1:p.Asn287=
NM_001005362.2:c.861C= NP_001005362.1:p.Asn287=
NM_001190716.1:c.861C= NP_001177645.1:p.Asn287=
NM_004945.3:c.861C= NP_004936.2:p.Asn287=
NM_001005361.3:c.861C= MANE Select NP_001005361.1:p.Asn287=
NM_001190716.2:c.861C= NP_001177645.1:p.Asn287=
NM_001005360.3:c.861C= NP_001005360.1:p.Asn287=
NM_001005362.3:c.861C= NP_001005362.1:p.Asn287=
NM_004945.4:c.861C= NP_004936.2:p.Asn287=