Canonical Allele Identifier: CA645619678

Gene: DNM2

Linked Data

• COSMIC: COSM5751912 ; COSM5751913 ; COSM5751914

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10793816_10793817insA , CM000681.2:g.10793816_10793817insA	GRCh38
NC_000019.9:g.10904492_10904493insA , CM000681.1:g.10904492_10904493insA	GRCh37
NC_000019.8:g.10765492_10765493insA	NCBI36
NG_008792.1:g.80738_80739insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000682285.1:n.1277_1278insA
ENST00000682524.1:n.1277_1278insA
ENST00000683738.1:n.1277_1278insA
ENST00000355667.11:c.1089_1090insA	ENSP00000347890.6:p.Arg364ThrfsTer10
ENST00000389253.9:c.1089_1090insA MANE Select	ENSP00000373905.4:p.Arg364ThrfsTer10
ENST00000355667.10:c.1089_1090insA	ENSP00000347890.6:p.Arg364ThrfsTer10
ENST00000359692.10:c.1089_1090insA	ENSP00000352721.6:p.Arg364ThrfsTer10
ENST00000389253.8:c.1089_1090insA	ENSP00000373905.3:p.Arg364ThrfsTer10
ENST00000408974.8:c.1089_1090insA	ENSP00000386192.3:p.Arg364ThrfsTer10
ENST00000585892.5:c.1089_1090insA	ENSP00000468734.1:p.Arg364ThrfsTer10
ENST00000587830.2:c.345_346insA	ENSP00000466603.2:p.Arg116ThrfsTer10
ENST00000591701.5:n.449_450insA
NM_001005360.2:c.1089_1090insA	NP_001005360.1:p.Arg364ThrfsTer10
NM_001005361.2:c.1089_1090insA	NP_001005361.1:p.Arg364ThrfsTer10
NM_001005362.2:c.1089_1090insA	NP_001005362.1:p.Arg364ThrfsTer10
NM_001190716.1:c.1089_1090insA	NP_001177645.1:p.Arg364ThrfsTer10
NM_004945.3:c.1089_1090insA	NP_004936.2:p.Arg364ThrfsTer10
NM_001005361.3:c.1089_1090insA MANE Select	NP_001005361.1:p.Arg364ThrfsTer10
NM_001190716.2:c.1089_1090insA	NP_001177645.1:p.Arg364ThrfsTer10
NM_001005360.3:c.1089_1090insA	NP_001005360.1:p.Arg364ThrfsTer10
NM_001005362.3:c.1089_1090insA	NP_001005362.1:p.Arg364ThrfsTer10
NM_004945.4:c.1089_1090insA	NP_004936.2:p.Arg364ThrfsTer10