Canonical Allele Identifier: CA2695232717
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32287692del , CM000685.2:g.32287692del GRCh38
NC_000023.10:g.32305809del , CM000685.1:g.32305809del GRCh37
NC_000023.9:g.32215730del NCBI36
NG_012232.1:g.1056918del , LRG_199:g.1056918del

Transcript Alleles

HGVS Amino-acid change
ENST00000358062.7:c.973del ENSP00000350765.3:p.Asp325IlefsTer30
ENST00000357033.9:c.6127del MANE Select ENSP00000354923.3:p.Asp2043IlefsTer30
ENST00000619831.5:c.2095del ENSP00000479270.2:p.Asp699IlefsTer30
ENST00000357033.8:c.6127del ENSP00000354923.3:p.Asp2043IlefsTer30
ENST00000378677.6:c.6115del ENSP00000367948.2:p.Asp2039IlefsTer30
ENST00000488902.5:n.336-70629del
ENST00000619831.4:c.6115del ENSP00000479270.1:p.Asp2039IlefsTer30
ENST00000620040.4:c.6127del ENSP00000478150.1:p.Asp2043IlefsTer30
NM_000109.3:c.6103del NP_000100.2:p.Asp2035IlefsTer30
NM_004006.2:c.6127del , LRG_199t1:c.6127del NP_003997.1:p.Asp2043IlefsTer30
NM_004009.3:c.6115del NP_004000.1:p.Asp2039IlefsTer30
NM_004010.3:c.5758del NP_004001.1:p.Asp1920IlefsTer30
NM_004011.3:c.2104del NP_004002.2:p.Asp702IlefsTer30
NM_004012.3:c.2095del NP_004003.1:p.Asp699IlefsTer30
XM_006724468.2:c.6127del XP_006724531.1:p.Asp2043IlefsTer30
XM_006724469.2:c.6103del XP_006724532.1:p.Asp2035IlefsTer30
XM_006724470.2:c.6127del XP_006724533.1:p.Asp2043IlefsTer30
XM_006724471.2:c.6127del XP_006724534.1:p.Asp2043IlefsTer30
XM_006724472.2:c.5998del XP_006724535.1:p.Asp2000IlefsTer30
XM_006724473.2:c.5989del XP_006724536.1:p.Asp1997IlefsTer30
XM_006724474.2:c.6127del XP_006724537.1:p.Asp2043IlefsTer30
XM_006724475.2:c.6127del XP_006724538.1:p.Asp2043IlefsTer30
XM_011545467.1:c.6004del XP_011543769.1:p.Asp2002IlefsTer30
XM_011545468.1:c.6127del XP_011543770.1:p.Asp2043IlefsTer30
XM_006724469.3:c.6103del XP_006724532.1:p.Asp2035IlefsTer30
XM_006724470.3:c.6127del XP_006724533.1:p.Asp2043IlefsTer30
XM_006724474.3:c.6127del XP_006724537.1:p.Asp2043IlefsTer30
XM_011545468.2:c.6127del XP_011543770.1:p.Asp2043IlefsTer30
XM_017029328.1:c.6127del XP_016884817.1:p.Asp2043IlefsTer30
XM_017029329.1:c.6127del XP_016884818.1:p.Asp2043IlefsTer30
XM_017029330.2:c.6127del XP_016884819.1:p.Asp2043IlefsTer30
XM_017029331.1:c.301del XP_016884820.1:p.Asp101IlefsTer30
NM_000109.4:c.6103del NP_000100.3:p.Asp2035IlefsTer30
NM_004006.3:c.6127del MANE Select NP_003997.2:p.Asp2043IlefsTer30
NM_004011.4:c.2104del NP_004002.3:p.Asp702IlefsTer30
NM_004012.4:c.2095del NP_004003.2:p.Asp699IlefsTer30