Canonical Allele Identifier: CA404040343

Gene: DNM2

Linked Data

• MyVariant Identifiers: chr19:g.10930675T>G (hg19) ; chr19:g.10819999T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10819999T>G , CM000681.2:g.10819999T>G	GRCh38
NC_000019.9:g.10930675T>G , CM000681.1:g.10930675T>G	GRCh37
NC_000019.8:g.10791675T>G	NCBI36
NG_008792.1:g.106921T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000681972.1:n.1122T>G
ENST00000355667.11:c.1691T>G	ENSP00000347890.6:p.Met564Arg
ENST00000389253.9:c.1691T>G MANE Select	ENSP00000373905.4:p.Met564Arg
ENST00000355667.10:c.1691T>G	ENSP00000347890.6:p.Met564Arg
ENST00000359692.10:c.1679T>G	ENSP00000352721.6:p.Met560Arg
ENST00000389253.8:c.1691T>G	ENSP00000373905.3:p.Met564Arg
ENST00000408974.8:c.1679T>G	ENSP00000386192.3:p.Met560Arg
ENST00000585892.5:c.1691T>G	ENSP00000468734.1:p.Met564Arg
ENST00000590787.1:n.3190T>G
ENST00000590806.5:n.3879T>G
NM_001005360.2:c.1691T>G	NP_001005360.1:p.Met564Arg
NM_001005361.2:c.1691T>G	NP_001005361.1:p.Met564Arg
NM_001005362.2:c.1679T>G	NP_001005362.1:p.Met560Arg
NM_001190716.1:c.1691T>G	NP_001177645.1:p.Met564Arg
NM_004945.3:c.1679T>G	NP_004936.2:p.Met560Arg
NM_001005361.3:c.1691T>G MANE Select	NP_001005361.1:p.Met564Arg
NM_001190716.2:c.1691T>G	NP_001177645.1:p.Met564Arg
NM_001005360.3:c.1691T>G	NP_001005360.1:p.Met564Arg
NM_001005362.3:c.1679T>G	NP_001005362.1:p.Met560Arg
NM_004945.4:c.1679T>G	NP_004936.2:p.Met560Arg