Canonical Allele Identifier: CA404048008

Gene: DNM2

Linked Data

• ClinVar Variation Id: 1060207
• ClinVar RCV Id: RCV001369603
• dbSNP Id: rs2146014211
• COSMIC: COSM3783170 ; COSM3783171 ; COSM3783172
• MyVariant Identifiers: chr19:g.10904491A>G (hg19) ; chr19:g.10793815A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10793815A>G , CM000681.2:g.10793815A>G	GRCh38
NC_000019.9:g.10904491A>G , CM000681.1:g.10904491A>G	GRCh37
NC_000019.8:g.10765491A>G	NCBI36
NG_008792.1:g.80737A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682285.1:n.1276A>G
ENST00000682524.1:n.1276A>G
ENST00000683738.1:n.1276A>G
ENST00000355667.11:c.1088A>G	ENSP00000347890.6:p.Asn363Ser
ENST00000389253.9:c.1088A>G MANE Select	ENSP00000373905.4:p.Asn363Ser
ENST00000355667.10:c.1088A>G	ENSP00000347890.6:p.Asn363Ser
ENST00000359692.10:c.1088A>G	ENSP00000352721.6:p.Asn363Ser
ENST00000389253.8:c.1088A>G	ENSP00000373905.3:p.Asn363Ser
ENST00000408974.8:c.1088A>G	ENSP00000386192.3:p.Asn363Ser
ENST00000585892.5:c.1088A>G	ENSP00000468734.1:p.Asn363Ser
ENST00000587830.2:c.344A>G	ENSP00000466603.2:p.Asn115Ser
ENST00000591701.5:n.448A>G
NM_001005360.2:c.1088A>G	NP_001005360.1:p.Asn363Ser
NM_001005361.2:c.1088A>G	NP_001005361.1:p.Asn363Ser
NM_001005362.2:c.1088A>G	NP_001005362.1:p.Asn363Ser
NM_001190716.1:c.1088A>G	NP_001177645.1:p.Asn363Ser
NM_004945.3:c.1088A>G	NP_004936.2:p.Asn363Ser
NM_001005361.3:c.1088A>G MANE Select	NP_001005361.1:p.Asn363Ser
NM_001190716.2:c.1088A>G	NP_001177645.1:p.Asn363Ser
NM_001005360.3:c.1088A>G	NP_001005360.1:p.Asn363Ser
NM_001005362.3:c.1088A>G	NP_001005362.1:p.Asn363Ser
NM_004945.4:c.1088A>G	NP_004936.2:p.Asn363Ser