Canonical Allele Identifier: CA2582429386
Gene: DNM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10772409T>C , CM000681.2:g.10772409T>C GRCh38
NC_000019.9:g.10883085T>C , CM000681.1:g.10883085T>C GRCh37
NC_000019.8:g.10744085T>C NCBI36
NG_008792.1:g.59331T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682285.1:n.424-70T>C
ENST00000682524.1:n.424-70T>C
ENST00000683738.1:n.424-70T>C
ENST00000355667.11:c.236-70T>C ENSP00000347890.6:n.236-70T>C
ENST00000389253.9:c.236-70T>C MANE Select ENSP00000373905.4:n.236-70T>C
ENST00000355667.10:c.236-70T>C ENSP00000347890.6:n.236-70T>C
ENST00000359692.10:c.236-70T>C ENSP00000352721.6:n.236-70T>C
ENST00000389253.8:c.236-70T>C ENSP00000373905.3:n.236-70T>C
ENST00000408974.8:c.236-70T>C ENSP00000386192.3:n.236-70T>C
ENST00000585892.5:c.236-70T>C ENSP00000468734.1:n.236-70T>C
ENST00000586939.5:c.-239-70T>C ENSP00000467430.1:n.-239-70T>C
ENST00000587991.5:n.311-70T>C
ENST00000591266.1:n.519-70T>C
ENST00000591819.1:n.159-70T>C
NM_001005360.2:c.236-70T>C NP_001005360.1:n.236-70T>C
NM_001005361.2:c.236-70T>C NP_001005361.1:n.236-70T>C
NM_001005362.2:c.236-70T>C NP_001005362.1:n.236-70T>C
NM_001190716.1:c.236-70T>C NP_001177645.1:n.236-70T>C
NM_004945.3:c.236-70T>C NP_004936.2:n.236-70T>C
NM_001005361.3:c.236-70T>C MANE Select NP_001005361.1:n.236-70T>C
NM_001190716.2:c.236-70T>C NP_001177645.1:n.236-70T>C
NM_001005360.3:c.236-70T>C NP_001005360.1:n.236-70T>C
NM_001005362.3:c.236-70T>C NP_001005362.1:n.236-70T>C
NM_004945.4:c.236-70T>C NP_004936.2:n.236-70T>C