Canonical Allele Identifier: CA404047828

Gene: DNM2

Linked Data

• dbSNP Id: rs759996048
• gnomAD v2: 19-10904407-A-G
• gnomAD v4: 19-10793731-A-G
• MyVariant Identifiers: chr19:g.10904407A>G (hg19) ; chr19:g.10793731A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10793731A>G , CM000681.2:g.10793731A>G	GRCh38
NC_000019.9:g.10904407A>G , CM000681.1:g.10904407A>G	GRCh37
NC_000019.8:g.10765407A>G	NCBI36
NG_008792.1:g.80653A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682285.1:n.1192A>G
ENST00000682524.1:n.1192A>G
ENST00000683738.1:n.1192A>G
ENST00000355667.11:c.1004A>G	ENSP00000347890.6:p.Gln335Arg
ENST00000389253.9:c.1004A>G MANE Select	ENSP00000373905.4:p.Gln335Arg
ENST00000355667.10:c.1004A>G	ENSP00000347890.6:p.Gln335Arg
ENST00000359692.10:c.1004A>G	ENSP00000352721.6:p.Gln335Arg
ENST00000389253.8:c.1004A>G	ENSP00000373905.3:p.Gln335Arg
ENST00000408974.8:c.1004A>G	ENSP00000386192.3:p.Gln335Arg
ENST00000585892.5:c.1004A>G	ENSP00000468734.1:p.Gln335Arg
ENST00000587485.1:n.510A>G
ENST00000587830.2:c.260A>G	ENSP00000466603.2:p.Gln87Arg
ENST00000591701.5:n.364A>G
NM_001005360.2:c.1004A>G	NP_001005360.1:p.Gln335Arg
NM_001005361.2:c.1004A>G	NP_001005361.1:p.Gln335Arg
NM_001005362.2:c.1004A>G	NP_001005362.1:p.Gln335Arg
NM_001190716.1:c.1004A>G	NP_001177645.1:p.Gln335Arg
NM_004945.3:c.1004A>G	NP_004936.2:p.Gln335Arg
NM_001005361.3:c.1004A>G MANE Select	NP_001005361.1:p.Gln335Arg
NM_001190716.2:c.1004A>G	NP_001177645.1:p.Gln335Arg
NM_001005360.3:c.1004A>G	NP_001005360.1:p.Gln335Arg
NM_001005362.3:c.1004A>G	NP_001005362.1:p.Gln335Arg
NM_004945.4:c.1004A>G	NP_004936.2:p.Gln335Arg