Canonical Allele Identifier: CA2322612570
Gene: DNM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10798450A= , CM000681.2:g.10798450A= GRCh38
NC_000019.9:g.10909126A= , CM000681.1:g.10909126A= GRCh37
NC_000019.8:g.10770126A= NCBI36
NG_008792.1:g.85372A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682285.1:n.1524-36A=
ENST00000683738.1:n.1663-36A=
ENST00000355667.11:c.1336-36A= ENSP00000347890.6:n.1336-36A=
ENST00000389253.9:c.1336-36A= MANE Select ENSP00000373905.4:n.1336-36A=
ENST00000355667.10:c.1336-36A= ENSP00000347890.6:n.1336-36A=
ENST00000359692.10:c.1336-36A= ENSP00000352721.6:n.1336-36A=
ENST00000389253.8:c.1336-36A= ENSP00000373905.3:n.1336-36A=
ENST00000408974.8:c.1336-36A= ENSP00000386192.3:n.1336-36A=
ENST00000585892.5:c.1336-36A= ENSP00000468734.1:n.1336-36A=
ENST00000587329.1:n.64A=
ENST00000587830.2:c.592-36A= ENSP00000466603.2:n.592-36A=
ENST00000593220.1:n.485-36A=
NM_001005360.2:c.1336-36A= NP_001005360.1:n.1336-36A=
NM_001005361.2:c.1336-36A= NP_001005361.1:n.1336-36A=
NM_001005362.2:c.1336-36A= NP_001005362.1:n.1336-36A=
NM_001190716.1:c.1336-36A= NP_001177645.1:n.1336-36A=
NM_004945.3:c.1336-36A= NP_004936.2:n.1336-36A=
NM_001005361.3:c.1336-36A= MANE Select NP_001005361.1:n.1336-36A=
NM_001190716.2:c.1336-36A= NP_001177645.1:n.1336-36A=
NM_001005360.3:c.1336-36A= NP_001005360.1:n.1336-36A=
NM_001005362.3:c.1336-36A= NP_001005362.1:n.1336-36A=
NM_004945.4:c.1336-36A= NP_004936.2:n.1336-36A=