Canonical Allele Identifier: CA1880160912
Gene: DNM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128219039C= , CM000671.2:g.128219039C= GRCh38
NC_000009.11:g.130981318C= , CM000671.1:g.130981318C= GRCh37
NC_000009.10:g.130021139C= NCBI36
NG_029726.1:g.20656C=

Transcript Alleles

HGVS Amino-acid change
ENST00000706053.1:c.386-10C= ENSP00000516205.1:n.386-10C=
ENST00000706054.1:c.21-10C=
ENST00000372923.8:c.386-10C= MANE Select ENSP00000362014.4:n.386-10C=
ENST00000634267.2:c.386-10C= ENSP00000489096.1:n.386-10C=
ENST00000636280.1:c.386-10C= ENSP00000490285.1:n.386-10C=
ENST00000637999.1:c.213-10C=
ENST00000341179.11:c.386-10C= ENSP00000345680.7:n.386-10C=
ENST00000372923.7:c.386-10C= ENSP00000362014.3:n.386-10C=
ENST00000393594.7:c.386-10C= ENSP00000377219.3:n.386-10C=
ENST00000441149.6:n.187-10C=
ENST00000475805.5:c.386-10C= ENSP00000419225.1:n.386-10C=
ENST00000486160.3:c.386-10C= ENSP00000420045.1:n.386-10C=
ENST00000627061.2:c.386-10C= ENSP00000486437.1:n.386-10C=
ENST00000627543.2:c.386-10C= ENSP00000487310.1:n.386-10C=
ENST00000628346.2:c.386-10C= ENSP00000486525.1:n.386-10C=
ENST00000634267.1:c.386-10C= ENSP00000489096.1:n.386-10C=
NM_001005336.2:c.386-10C= NP_001005336.1:n.386-10C=
NM_001288737.1:c.386-10C= NP_001275666.1:n.386-10C=
NM_001288738.1:c.386-10C= NP_001275667.1:n.386-10C=
NM_001288739.1:c.386-10C= NP_001275668.1:n.386-10C=
NM_004408.3:c.386-10C= NP_004399.2:n.386-10C=
XM_005251763.1:c.386-10C= XP_005251820.1:n.386-10C=
XM_005251764.1:c.386-10C= XP_005251821.1:n.386-10C=
XM_005251768.1:c.386-10C= XP_005251825.1:n.386-10C=
XM_005251769.1:c.386-10C= XP_005251826.1:n.386-10C=
XM_006716992.1:c.386-10C= XP_006717055.1:n.386-10C=
XM_006716993.1:c.386-10C= XP_006717056.1:n.386-10C=
XM_011518334.1:c.386-10C= XP_011516636.1:n.386-10C=
XM_011518335.1:c.386-10C= XP_011516637.1:n.386-10C=
XM_011518336.1:c.386-10C= XP_011516638.1:n.386-10C=
XM_011518337.1:c.386-10C= XP_011516639.1:n.386-10C=
XM_011518338.1:c.386-10C= XP_011516640.1:n.386-10C=
XR_242572.1:n.502-10C=
XR_242573.2:n.502-10C=
XR_929729.1:n.502-10C=
XR_929730.1:n.502-10C=
XM_005251763.3:c.386-10C= XP_005251820.1:n.386-10C=
XM_005251768.3:c.386-10C= XP_005251825.1:n.386-10C=
XM_005251769.3:c.386-10C= XP_005251826.1:n.386-10C=
XM_006716992.3:c.386-10C= XP_006717055.1:n.386-10C=
XM_006716993.2:c.386-10C= XP_006717056.1:n.386-10C=
XM_011518335.3:c.386-10C= XP_011516637.1:n.386-10C=
XM_011518336.3:c.386-10C= XP_011516638.1:n.386-10C=
XM_017014369.2:c.386-10C= XP_016869858.1:n.386-10C=
XM_017014370.2:c.386-10C= XP_016869859.1:n.386-10C=
XM_017014371.2:c.386-10C= XP_016869860.1:n.386-10C=
XM_017014372.2:c.386-10C= XP_016869861.1:n.386-10C=
XM_017014373.2:c.386-10C= XP_016869862.1:n.386-10C=
XR_001746219.2:n.478-10C=
XR_001746220.2:n.478-10C=
XR_001746221.2:n.478-10C=
XR_001746222.2:n.478-10C=
NM_001005336.3:c.386-10C= NP_001005336.1:n.386-10C=
NM_001288737.2:c.386-10C= NP_001275666.1:n.386-10C=
NM_001288738.2:c.386-10C= NP_001275667.1:n.386-10C=
NM_001288739.2:c.386-10C= NP_001275668.1:n.386-10C=
NM_001374269.1:c.386-10C= NP_001361198.1:n.386-10C=
NM_004408.4:c.386-10C= MANE Select NP_004399.2:n.386-10C=