Canonical Allele Identifier: CA505492335

Gene: DNM2

Linked Data

• MyVariant Identifiers: chr19:g.10883156A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10772480A>G , CM000681.2:g.10772480A>G	GRCh38
NC_000019.9:g.10883156A>G , CM000681.1:g.10883156A>G	GRCh37
NC_000019.8:g.10744156A>G	NCBI36
NG_008792.1:g.59402A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682285.1:n.425A>G
ENST00000682524.1:n.425A>G
ENST00000683738.1:n.425A>G
ENST00000355667.11:c.237A>G	ENSP00000347890.6:p.Glu79=
ENST00000389253.9:c.237A>G MANE Select	ENSP00000373905.4:p.Glu79=
ENST00000355667.10:c.237A>G	ENSP00000347890.6:p.Glu79=
ENST00000359692.10:c.237A>G	ENSP00000352721.6:p.Glu79=
ENST00000389253.8:c.237A>G	ENSP00000373905.3:p.Glu79=
ENST00000408974.8:c.237A>G	ENSP00000386192.3:p.Glu79=
ENST00000585892.5:c.237A>G	ENSP00000468734.1:p.Glu79=
ENST00000586939.5:c.-238A>G	ENSP00000467430.1:n.-238A>G
ENST00000587991.5:n.312A>G
ENST00000591266.1:n.520A>G
ENST00000591819.1:n.160A>G
NM_001005360.2:c.237A>G	NP_001005360.1:p.Glu79=
NM_001005361.2:c.237A>G	NP_001005361.1:p.Glu79=
NM_001005362.2:c.237A>G	NP_001005362.1:p.Glu79=
NM_001190716.1:c.237A>G	NP_001177645.1:p.Glu79=
NM_004945.3:c.237A>G	NP_004936.2:p.Glu79=
NM_001005361.3:c.237A>G MANE Select	NP_001005361.1:p.Glu79=
NM_001190716.2:c.237A>G	NP_001177645.1:p.Glu79=
NM_001005360.3:c.237A>G	NP_001005360.1:p.Glu79=
NM_001005362.3:c.237A>G	NP_001005362.1:p.Glu79=
NM_004945.4:c.237A>G	NP_004936.2:p.Glu79=