Canonical Allele Identifier: CA2322600605
Gene: DNM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10772499T= , CM000681.2:g.10772499T= GRCh38
NC_000019.9:g.10883175T= , CM000681.1:g.10883175T= GRCh37
NC_000019.8:g.10744175T= NCBI36
NG_008792.1:g.59421T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682285.1:n.444T=
ENST00000682524.1:n.444T=
ENST00000683738.1:n.444T=
ENST00000355667.11:c.256T= ENSP00000347890.6:p.Cys86=
ENST00000389253.9:c.256T= MANE Select ENSP00000373905.4:p.Cys86=
ENST00000355667.10:c.256T= ENSP00000347890.6:p.Cys86=
ENST00000359692.10:c.256T= ENSP00000352721.6:p.Cys86=
ENST00000389253.8:c.256T= ENSP00000373905.3:p.Cys86=
ENST00000408974.8:c.256T= ENSP00000386192.3:p.Cys86=
ENST00000585892.5:c.256T= ENSP00000468734.1:p.Cys86=
ENST00000586939.5:c.-219T= ENSP00000467430.1:n.-219T=
ENST00000587991.5:n.331T=
ENST00000591266.1:n.539T=
ENST00000591819.1:n.179T=
NM_001005360.2:c.256T= NP_001005360.1:p.Cys86=
NM_001005361.2:c.256T= NP_001005361.1:p.Cys86=
NM_001005362.2:c.256T= NP_001005362.1:p.Cys86=
NM_001190716.1:c.256T= NP_001177645.1:p.Cys86=
NM_004945.3:c.256T= NP_004936.2:p.Cys86=
NM_001005361.3:c.256T= MANE Select NP_001005361.1:p.Cys86=
NM_001190716.2:c.256T= NP_001177645.1:p.Cys86=
NM_001005360.3:c.256T= NP_001005360.1:p.Cys86=
NM_001005362.3:c.256T= NP_001005362.1:p.Cys86=
NM_004945.4:c.256T= NP_004936.2:p.Cys86=