Canonical Allele Identifier: CA2322600544
Gene: DNM2 HGNC NCBI

Linked Data

dbSNP Id: rs2071010527

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10772311C>T , CM000681.2:g.10772311C>T GRCh38
NC_000019.9:g.10882987C>T , CM000681.1:g.10882987C>T GRCh37
NC_000019.8:g.10743987C>T NCBI36
NG_008792.1:g.59233C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682285.1:n.424-168C>T
ENST00000682524.1:n.424-168C>T
ENST00000683738.1:n.424-168C>T
ENST00000355667.11:c.236-168C>T ENSP00000347890.6:n.236-168C>T
ENST00000389253.9:c.236-168C>T MANE Select ENSP00000373905.4:n.236-168C>T
ENST00000355667.10:c.236-168C>T ENSP00000347890.6:n.236-168C>T
ENST00000359692.10:c.236-168C>T ENSP00000352721.6:n.236-168C>T
ENST00000389253.8:c.236-168C>T ENSP00000373905.3:n.236-168C>T
ENST00000408974.8:c.236-168C>T ENSP00000386192.3:n.236-168C>T
ENST00000585892.5:c.236-168C>T ENSP00000468734.1:n.236-168C>T
ENST00000586939.5:c.-239-168C>T ENSP00000467430.1:n.-239-168C>T
ENST00000587991.5:n.311-168C>T
ENST00000591266.1:n.519-168C>T
ENST00000591819.1:n.159-168C>T
NM_001005360.2:c.236-168C>T NP_001005360.1:n.236-168C>T
NM_001005361.2:c.236-168C>T NP_001005361.1:n.236-168C>T
NM_001005362.2:c.236-168C>T NP_001005362.1:n.236-168C>T
NM_001190716.1:c.236-168C>T NP_001177645.1:n.236-168C>T
NM_004945.3:c.236-168C>T NP_004936.2:n.236-168C>T
NM_001005361.3:c.236-168C>T MANE Select NP_001005361.1:n.236-168C>T
NM_001190716.2:c.236-168C>T NP_001177645.1:n.236-168C>T
NM_001005360.3:c.236-168C>T NP_001005360.1:n.236-168C>T
NM_001005362.3:c.236-168C>T NP_001005362.1:n.236-168C>T
NM_004945.4:c.236-168C>T NP_004936.2:n.236-168C>T