Canonical Allele Identifier: CA2322607160
Gene: DNM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10786576C= , CM000681.2:g.10786576C= GRCh38
NC_000019.9:g.10897252C= , CM000681.1:g.10897252C= GRCh37
NC_000019.8:g.10758252C= NCBI36
NG_008792.1:g.73498C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682285.1:n.1050C=
ENST00000682524.1:n.1050C=
ENST00000683738.1:n.1050C=
ENST00000355667.11:c.862C= ENSP00000347890.6:p.His288=
ENST00000389253.9:c.862C= MANE Select ENSP00000373905.4:p.His288=
ENST00000355667.10:c.862C= ENSP00000347890.6:p.His288=
ENST00000359692.10:c.862C= ENSP00000352721.6:p.His288=
ENST00000389253.8:c.862C= ENSP00000373905.3:p.His288=
ENST00000408974.8:c.862C= ENSP00000386192.3:p.His288=
ENST00000585892.5:c.862C= ENSP00000468734.1:p.His288=
ENST00000586130.1:n.147C=
ENST00000587485.1:n.368C=
ENST00000587830.2:c.118C= ENSP00000466603.2:p.His40=
ENST00000591701.5:n.222C=
NM_001005360.2:c.862C= NP_001005360.1:p.His288=
NM_001005361.2:c.862C= NP_001005361.1:p.His288=
NM_001005362.2:c.862C= NP_001005362.1:p.His288=
NM_001190716.1:c.862C= NP_001177645.1:p.His288=
NM_004945.3:c.862C= NP_004936.2:p.His288=
NM_001005361.3:c.862C= MANE Select NP_001005361.1:p.His288=
NM_001190716.2:c.862C= NP_001177645.1:p.His288=
NM_001005360.3:c.862C= NP_001005360.1:p.His288=
NM_001005362.3:c.862C= NP_001005362.1:p.His288=
NM_004945.4:c.862C= NP_004936.2:p.His288=