Canonical Allele Identifier: CA2582431002
Gene: DNM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10793639_10793640insG , CM000681.2:g.10793639_10793640insG GRCh38
NC_000019.9:g.10904315_10904316insG , CM000681.1:g.10904315_10904316insG GRCh37
NC_000019.8:g.10765315_10765316insG NCBI36
NG_008792.1:g.80561_80562insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682285.1:n.1181-81_1181-80insG
ENST00000682524.1:n.1181-81_1181-80insG
ENST00000683738.1:n.1181-81_1181-80insG
ENST00000355667.11:c.993-81_993-80insG ENSP00000347890.6:n.993-81_993-80insG
ENST00000389253.9:c.993-81_993-80insG MANE Select ENSP00000373905.4:n.993-81_993-80insG
ENST00000355667.10:c.993-81_993-80insG ENSP00000347890.6:n.993-81_993-80insG
ENST00000359692.10:c.993-81_993-80insG ENSP00000352721.6:n.993-81_993-80insG
ENST00000389253.8:c.993-81_993-80insG ENSP00000373905.3:n.993-81_993-80insG
ENST00000408974.8:c.993-81_993-80insG ENSP00000386192.3:n.993-81_993-80insG
ENST00000585892.5:c.993-81_993-80insG ENSP00000468734.1:n.993-81_993-80insG
ENST00000587485.1:n.499-81_499-80insG
ENST00000587830.2:c.249-81_249-80insG ENSP00000466603.2:n.249-81_249-80insG
ENST00000591701.5:n.353-81_353-80insG
NM_001005360.2:c.993-81_993-80insG NP_001005360.1:n.993-81_993-80insG
NM_001005361.2:c.993-81_993-80insG NP_001005361.1:n.993-81_993-80insG
NM_001005362.2:c.993-81_993-80insG NP_001005362.1:n.993-81_993-80insG
NM_001190716.1:c.993-81_993-80insG NP_001177645.1:n.993-81_993-80insG
NM_004945.3:c.993-81_993-80insG NP_004936.2:n.993-81_993-80insG
NM_001005361.3:c.993-81_993-80insG MANE Select NP_001005361.1:n.993-81_993-80insG
NM_001190716.2:c.993-81_993-80insG NP_001177645.1:n.993-81_993-80insG
NM_001005360.3:c.993-81_993-80insG NP_001005360.1:n.993-81_993-80insG
NM_001005362.3:c.993-81_993-80insG NP_001005362.1:n.993-81_993-80insG
NM_004945.4:c.993-81_993-80insG NP_004936.2:n.993-81_993-80insG