Canonical Allele Identifier: CA9200805
Gene: DNM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10775788G>A , CM000681.2:g.10775788G>A GRCh38
NC_000019.9:g.10886464G>A , CM000681.1:g.10886464G>A GRCh37
NC_000019.8:g.10747464G>A NCBI36
NG_008792.1:g.62710G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682285.1:n.659G>A
ENST00000682524.1:n.659G>A
ENST00000683738.1:n.659G>A
ENST00000355667.11:c.471G>A ENSP00000347890.6:p.Lys157=
ENST00000389253.9:c.471G>A MANE Select ENSP00000373905.4:p.Lys157=
ENST00000355667.10:c.471G>A ENSP00000347890.6:p.Lys157=
ENST00000359692.10:c.471G>A ENSP00000352721.6:p.Lys157=
ENST00000389253.8:c.471G>A ENSP00000373905.3:p.Lys157=
ENST00000408974.8:c.471G>A ENSP00000386192.3:p.Lys157=
ENST00000585892.5:c.471G>A ENSP00000468734.1:p.Lys157=
ENST00000586939.5:c.-4G>A ENSP00000467430.1:n.-4G>A
ENST00000587991.5:n.546G>A
ENST00000591819.1:n.394G>A
NM_001005360.2:c.471G>A NP_001005360.1:p.Lys157=
NM_001005361.2:c.471G>A NP_001005361.1:p.Lys157=
NM_001005362.2:c.471G>A NP_001005362.1:p.Lys157=
NM_001190716.1:c.471G>A NP_001177645.1:p.Lys157=
NM_004945.3:c.471G>A NP_004936.2:p.Lys157=
NM_001005361.3:c.471G>A MANE Select NP_001005361.1:p.Lys157=
NM_001190716.2:c.471G>A NP_001177645.1:p.Lys157=
NM_001005360.3:c.471G>A NP_001005360.1:p.Lys157=
NM_001005362.3:c.471G>A NP_001005362.1:p.Lys157=
NM_004945.4:c.471G>A NP_004936.2:p.Lys157=