Canonical Allele Identifier: CA2322624779

Gene: DNM2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10823862C= , CM000681.2:g.10823862C=	GRCh38
NC_000019.9:g.10934538C= , CM000681.1:g.10934538C=	GRCh37
NC_000019.8:g.10795538C=	NCBI36
NG_008792.1:g.110784C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001005361.3:c.1856C= MANE Select	NP_001005361.1:p.Ser619=
ENST00000389253.9:c.1856C= MANE Select	ENSP00000373905.4:p.Ser619=
NM_001005360.2:c.1856C=	NP_001005360.1:p.Ser619=
NM_001005360.3:c.1856C=	NP_001005360.1:p.Ser619=
NM_001005361.2:c.1856C=	NP_001005361.1:p.Ser619=
NM_001005362.2:c.1844C=	NP_001005362.1:p.Ser615=
NM_001005362.3:c.1844C=	NP_001005362.1:p.Ser615=
NM_001190716.1:c.1856C=	NP_001177645.1:p.Ser619=
NM_001190716.2:c.1856C=	NP_001177645.1:p.Ser619=
NM_004945.3:c.1844C=	NP_004936.2:p.Ser615=
NM_004945.4:c.1844C=	NP_004936.2:p.Ser615=
ENST00000355667.10:c.1856C=	ENSP00000347890.6:p.Ser619=
ENST00000355667.11:c.1856C=	ENSP00000347890.6:p.Ser619=
ENST00000359692.10:c.1844C=	ENSP00000352721.6:p.Ser615=
ENST00000389253.8:c.1856C=	ENSP00000373905.3:p.Ser619=
ENST00000408974.8:c.1844C=	ENSP00000386192.3:p.Ser615=
ENST00000585892.5:c.1856C=	ENSP00000468734.1:p.Ser619=
ENST00000590787.1:n.3355C=
ENST00000590806.5:n.4044C=
ENST00000593203.1:n.639C=
ENST00000681972.1:n.1287C=