Canonical Allele Identifier: CA2695232435
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.31773979del , CM000685.2:g.31773979del GRCh38
NC_000023.10:g.31792096del , CM000685.1:g.31792096del GRCh37
NC_000023.9:g.31702017del NCBI36
NG_012232.1:g.1570631del , LRG_199:g.1570631del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358062.7:c.2369del ENSP00000350765.3:p.Glu790GlyfsTer2
ENST00000682238.1:c.143del ENSP00000508124.1:p.Glu48GlyfsTer2
ENST00000683117.1:n.1184del
ENST00000683450.1:n.1106del
ENST00000683851.1:n.1184del
ENST00000683957.1:n.1015del
ENST00000684130.1:c.143del ENSP00000508037.1:p.Glu48GlyfsTer2
ENST00000357033.9:c.7523del MANE Select ENSP00000354923.3:p.Glu2508GlyfsTer2
ENST00000619831.5:c.3491del ENSP00000479270.2:p.Glu1164GlyfsTer2
ENST00000620040.5:c.143del ENSP00000478150.2:p.Glu48GlyfsTer2
ENST00000680961.1:c.143del ENSP00000506386.1:p.Glu48GlyfsTer2
ENST00000681646.1:n.1184del
ENST00000681839.1:c.512del ENSP00000505228.1:p.Glu171GlyfsTer2
ENST00000357033.8:c.7523del ENSP00000354923.3:p.Glu2508GlyfsTer2
ENST00000358062.6:c.611del ENSP00000350765.2:p.Glu204GlyfsTer2
ENST00000359836.5:c.143del ENSP00000352894.1:p.Glu48GlyfsTer2
ENST00000378677.6:c.7511del ENSP00000367948.2:p.Glu2504GlyfsTer2
ENST00000378707.7:c.143del ENSP00000367979.3:p.Glu48GlyfsTer2
ENST00000471779.1:c.280del ENSP00000417075.1:n.280del
ENST00000474231.5:c.143del ENSP00000417123.1:p.Glu48GlyfsTer2
ENST00000541735.5:c.143del ENSP00000444119.1:p.Glu48GlyfsTer2
ENST00000619831.4:c.7508del ENSP00000479270.1:p.Glu2503GlyfsTer2
ENST00000620040.4:c.7520del ENSP00000478150.1:p.Glu2507GlyfsTer2
NM_000109.3:c.7499del NP_000100.2:p.Glu2500GlyfsTer2
NM_004006.2:c.7523del , LRG_199t1:c.7523del NP_003997.1:p.Glu2508GlyfsTer2
NM_004009.3:c.7511del NP_004000.1:p.Glu2504GlyfsTer2
NM_004010.3:c.7154del NP_004001.1:p.Glu2385GlyfsTer2
NM_004011.3:c.3500del NP_004002.2:p.Glu1167GlyfsTer2
NM_004012.3:c.3491del NP_004003.1:p.Glu1164GlyfsTer2
NM_004013.2:c.143del NP_004004.1:p.Glu48GlyfsTer2
NM_004020.3:c.143del NP_004011.2:p.Glu48GlyfsTer2
NM_004021.2:c.143del NP_004012.1:p.Glu48GlyfsTer2
NM_004022.2:c.143del NP_004013.1:p.Glu48GlyfsTer2
NM_004023.2:c.143del NP_004014.1:p.Glu48GlyfsTer2
XM_006724468.2:c.7523del XP_006724531.1:p.Glu2508GlyfsTer2
XM_006724469.2:c.7499del XP_006724532.1:p.Glu2500GlyfsTer2
XM_006724470.2:c.7523del XP_006724533.1:p.Glu2508GlyfsTer2
XM_006724471.2:c.7523del XP_006724534.1:p.Glu2508GlyfsTer2
XM_006724472.2:c.7394del XP_006724535.1:p.Glu2465GlyfsTer2
XM_006724473.2:c.7385del XP_006724536.1:p.Glu2462GlyfsTer2
XM_006724474.2:c.7523del XP_006724537.1:p.Glu2508GlyfsTer2
XM_006724475.2:c.7523del XP_006724538.1:p.Glu2508GlyfsTer2
XM_011545467.1:c.7400del XP_011543769.1:p.Glu2467GlyfsTer2
XM_011545468.1:c.7523del XP_011543770.1:p.Glu2508GlyfsTer2
XM_006724469.3:c.7499del XP_006724532.1:p.Glu2500GlyfsTer2
XM_006724470.3:c.7523del XP_006724533.1:p.Glu2508GlyfsTer2
XM_006724474.3:c.7523del XP_006724537.1:p.Glu2508GlyfsTer2
XM_011545468.2:c.7523del XP_011543770.1:p.Glu2508GlyfsTer2
XM_017029328.1:c.7523del XP_016884817.1:p.Glu2508GlyfsTer2
XM_017029331.1:c.1697del XP_016884820.1:p.Glu566GlyfsTer2
NM_000109.4:c.7499del NP_000100.3:p.Glu2500GlyfsTer2
NM_004006.3:c.7523del MANE Select NP_003997.2:p.Glu2508GlyfsTer2
NM_004011.4:c.3500del NP_004002.3:p.Glu1167GlyfsTer2
NM_004012.4:c.3491del NP_004003.2:p.Glu1164GlyfsTer2
NM_004021.3:c.143del NP_004012.2:p.Glu48GlyfsTer2
NM_004023.3:c.143del NP_004014.2:p.Glu48GlyfsTer2
NM_004013.3:c.143del NP_004004.2:p.Glu48GlyfsTer2
NM_004020.4:c.143del NP_004011.3:p.Glu48GlyfsTer2
NM_004022.3:c.143del NP_004013.2:p.Glu48GlyfsTer2