Canonical Allele Identifier: CA505494730

Gene: DNM2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10831023A>C , CM000681.2:g.10831023A>C	GRCh38
NC_000019.9:g.10941699A>C , CM000681.1:g.10941699A>C	GRCh37
NC_000019.8:g.10802699A>C	NCBI36
NG_008792.1:g.117945A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681972.1:n.2020A>C
ENST00000355667.11:c.2589A>C	ENSP00000347890.6:p.Pro863=
ENST00000389253.9:c.2589A>C MANE Select	ENSP00000373905.4:p.Pro863=
ENST00000355667.10:c.2589A>C	ENSP00000347890.6:p.Pro863=
ENST00000359692.10:c.2577A>C	ENSP00000352721.6:p.Pro859=
ENST00000389253.8:c.2589A>C	ENSP00000373905.3:p.Pro863=
ENST00000408974.8:c.2577A>C	ENSP00000386192.3:p.Pro859=
ENST00000585892.5:c.2586A>C	ENSP00000468734.1:p.Pro862=
ENST00000590806.5:n.4777A>C
ENST00000591818.1:c.41+645A>C	ENSP00000466621.1:n.41+645A>C
ENST00000593203.1:n.1326+645A>C
NM_001005360.2:c.2589A>C	NP_001005360.1:p.Pro863=
NM_001005361.2:c.2589A>C	NP_001005361.1:p.Pro863=
NM_001005362.2:c.2577A>C	NP_001005362.1:p.Pro859=
NM_001190716.1:c.2586A>C	NP_001177645.1:p.Pro862=
NM_004945.3:c.2577A>C	NP_004936.2:p.Pro859=
NM_001005361.3:c.2589A>C MANE Select	NP_001005361.1:p.Pro863=
NM_001190716.2:c.2586A>C	NP_001177645.1:p.Pro862=
NM_001005360.3:c.2589A>C	NP_001005360.1:p.Pro863=
NM_001005362.3:c.2577A>C	NP_001005362.1:p.Pro859=
NM_004945.4:c.2577A>C	NP_004936.2:p.Pro859=