Canonical Allele Identifier: CA16616478
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 409933
dbSNP Id: rs1060502653

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.31204118_31204127del , CM000685.2:g.31204118_31204127del GRCh38
NC_000023.10:g.31222235_31222244del , CM000685.1:g.31222235_31222244del GRCh37
NC_000023.9:g.31132156_31132165del NCBI36
NG_012232.1:g.2140488_2140497del , LRG_199:g.2140488_2140497del

Transcript Alleles

HGVS Amino-acid change
ENST00000358062.7:c.4496-4_4501del
ENST00000680162.2:c.446-4_451del
ENST00000680768.2:c.446-4_451del
ENST00000681989.1:n.448-4_453del
ENST00000682238.1:c.2270-4_2275del
ENST00000682322.1:c.446-4_451del
ENST00000682600.1:c.446-4_451del
ENST00000682769.1:n.448-4_453del
ENST00000683509.1:n.1167-4_1172del
ENST00000683675.1:n.749-4_754del
ENST00000683709.1:n.1168-4_1173del
ENST00000683957.1:n.3142-4_3147del
ENST00000684130.1:c.2270-4_2275del
ENST00000343523.7:c.1505-4_1510del
ENST00000357033.9:c.9650-4_9655del
ENST00000619831.5:c.5618-4_5623del
ENST00000620040.5:c.2270-4_2275del
ENST00000679641.1:c.446-4_451del
ENST00000680162.1:c.323-4_328del
ENST00000680355.1:c.446-4_451del
ENST00000680557.1:c.446-4_451del
ENST00000680768.1:c.389-4_394del
ENST00000680961.1:c.2270-4_2275del
ENST00000681153.1:c.446-4_451del
ENST00000681334.1:c.446-4_451del
ENST00000681654.1:n.580-4_585del
ENST00000343523.6:c.1463-4_1468del
ENST00000357033.8:c.9650-4_9655del
ENST00000358062.6:c.2738-4_2743del
ENST00000359836.5:c.2270-4_2275del
ENST00000361471.8:c.446-4_451del
ENST00000378677.6:c.9638-4_9643del
ENST00000378680.6:c.446-4_451del
ENST00000378702.8:c.446-4_451del
ENST00000378705.3:c.20-4_25del
ENST00000378707.7:c.2270-4_2275del
ENST00000378723.7:c.446-4_451del
ENST00000474231.5:c.2270-4_2275del
ENST00000541735.5:c.2270-4_2275del
ENST00000619831.4:c.9635-4_9640del
ENST00000620040.4:c.9647-4_9652del
NM_000109.3:c.9626-4_9631del
NM_004006.2:c.9650-4_9655del , LRG_199t1:c.9650-4_9655del
NM_004009.3:c.9638-4_9643del
NM_004010.3:c.9281-4_9286del
NM_004011.3:c.5627-4_5632del
NM_004012.3:c.5618-4_5623del
NM_004013.2:c.2270-4_2275del
NM_004014.2:c.1463-4_1468del
NM_004015.2:c.446-4_451del
NM_004016.2:c.446-4_451del
NM_004017.2:c.446-4_451del
NM_004018.2:c.446-4_451del
NM_004019.2:c.446-4_451del
NM_004020.3:c.2270-4_2275del
NM_004021.2:c.2270-4_2275del
NM_004022.2:c.2270-4_2275del
NM_004023.2:c.2270-4_2275del
XM_006724468.2:c.9650-4_9655del
XM_006724469.2:c.9626-4_9631del
XM_006724470.2:c.9650-4_9655del
XM_006724471.2:c.9650-4_9655del
XM_006724472.2:c.9521-4_9526del
XM_006724473.2:c.9512-4_9517del
XM_006724474.2:c.9650-4_9655del
XM_006724475.2:c.9650-4_9655del
XM_011545467.1:c.9527-4_9532del
XM_011545468.1:c.9650-4_9655del
XM_006724469.3:c.9626-4_9631del
XM_006724470.3:c.9650-4_9655del
XM_006724474.3:c.9650-4_9655del
XM_011545468.2:c.9650-4_9655del
XM_017029328.1:c.9650-4_9655del
XM_017029331.1:c.3824-4_3829del
NM_000109.4:c.9626-4_9631del
NM_004006.3:c.9650-4_9655del
NM_004011.4:c.5627-4_5632del
NM_004012.4:c.5618-4_5623del
NM_004015.3:c.446-4_451del
NM_004016.3:c.446-4_451del
NM_004017.3:c.446-4_451del
NM_004018.3:c.446-4_451del
NM_004019.3:c.446-4_451del
NM_004021.3:c.2270-4_2275del
NM_004023.3:c.2270-4_2275del
NM_004013.3:c.2270-4_2275del
NM_004014.3:c.1463-4_1468del
NM_004020.4:c.2270-4_2275del
NM_004022.3:c.2270-4_2275del