Canonical Allele Identifier: CA412653221
Gene: DMD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.31180470A>T , CM000685.2:g.31180470A>T GRCh38
NC_000023.10:g.31198587A>T , CM000685.1:g.31198587A>T GRCh37
NC_000023.9:g.31108508A>T NCBI36
NG_012232.1:g.2164140T>A , LRG_199:g.2164140T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000358062.7:c.4832T>A ENSP00000350765.3:p.Leu1611Gln
ENST00000475732.3:n.2333T>A
ENST00000680162.2:c.782T>A ENSP00000506634.2:p.Leu261Gln
ENST00000680768.2:c.782T>A ENSP00000506359.2:p.Leu261Gln
ENST00000681989.1:n.784T>A
ENST00000682238.1:c.2606T>A ENSP00000508124.1:p.Leu869Gln
ENST00000682322.1:c.782T>A ENSP00000507690.1:p.Leu261Gln
ENST00000682600.1:c.782T>A ENSP00000507640.1:p.Leu261Gln
ENST00000682769.1:n.617T>A
ENST00000683509.1:n.1503T>A
ENST00000683675.1:n.1085T>A
ENST00000683709.1:n.1504T>A
ENST00000683957.1:n.3478T>A
ENST00000684130.1:c.2606T>A ENSP00000508037.1:p.Leu869Gln
ENST00000343523.7:c.1841T>A ENSP00000340057.4:p.Leu614Gln
ENST00000357033.9:c.9986T>A MANE Select ENSP00000354923.3:p.Leu3329Gln
ENST00000475732.2:n.352T>A
ENST00000619831.5:c.5954T>A ENSP00000479270.2:p.Leu1985Gln
ENST00000620040.5:c.2606T>A ENSP00000478150.2:p.Leu869Gln
ENST00000679641.1:c.615T>A ENSP00000506135.1:p.Ser205=
ENST00000680162.1:c.659T>A ENSP00000506634.1:p.Leu220Gln
ENST00000680355.1:c.782T>A ENSP00000506257.1:p.Leu261Gln
ENST00000680557.1:c.603+23491T>A ENSP00000505164.1:n.603+23491T>A
ENST00000680768.1:c.725T>A ENSP00000506359.1:p.Leu242Gln
ENST00000680961.1:c.2439T>A ENSP00000506386.1:p.Ser813=
ENST00000681153.1:c.782T>A ENSP00000505124.1:p.Leu261Gln
ENST00000681654.1:n.916T>A
ENST00000343523.6:c.1799T>A ENSP00000340057.3:p.Leu600Gln
ENST00000357033.8:c.9986T>A ENSP00000354923.3:p.Leu3329Gln
ENST00000358062.6:c.3074T>A ENSP00000350765.2:p.Leu1025Gln
ENST00000359836.5:c.2606T>A ENSP00000352894.1:p.Leu869Gln
ENST00000361471.8:c.782T>A ENSP00000354464.4:p.Leu261Gln
ENST00000378677.6:c.9974T>A ENSP00000367948.2:p.Leu3325Gln
ENST00000378680.6:c.782T>A ENSP00000367951.2:p.Leu261Gln
ENST00000378702.8:c.782T>A ENSP00000367974.4:p.Leu261Gln
ENST00000378705.3:c.356T>A ENSP00000367977.3:p.Leu119Gln
ENST00000378707.7:c.2606T>A ENSP00000367979.3:p.Leu869Gln
ENST00000378723.7:c.782T>A ENSP00000367997.3:p.Leu261Gln
ENST00000474231.5:c.2606T>A ENSP00000417123.1:p.Leu869Gln
ENST00000475732.1:n.202T>A
ENST00000541735.5:c.2606T>A ENSP00000444119.1:p.Leu869Gln
ENST00000619831.4:c.9971T>A ENSP00000479270.1:p.Leu3324Gln
ENST00000620040.4:c.9983T>A ENSP00000478150.1:p.Leu3328Gln
NM_000109.3:c.9962T>A NP_000100.2:p.Leu3321Gln
NM_004006.2:c.9986T>A , LRG_199t1:c.9986T>A NP_003997.1:p.Leu3329Gln
NM_004009.3:c.9974T>A NP_004000.1:p.Leu3325Gln
NM_004010.3:c.9617T>A NP_004001.1:p.Leu3206Gln
NM_004011.3:c.5963T>A NP_004002.2:p.Leu1988Gln
NM_004012.3:c.5954T>A NP_004003.1:p.Leu1985Gln
NM_004013.2:c.2606T>A NP_004004.1:p.Leu869Gln
NM_004014.2:c.1799T>A NP_004005.1:p.Leu600Gln
NM_004015.2:c.782T>A NP_004006.1:p.Leu261Gln
NM_004016.2:c.782T>A NP_004007.1:p.Leu261Gln
NM_004017.2:c.782T>A NP_004008.1:p.Leu261Gln
NM_004018.2:c.782T>A NP_004009.1:p.Leu261Gln
NM_004019.2:c.782T>A NP_004010.1:p.Leu261Gln
NM_004020.3:c.2606T>A NP_004011.2:p.Leu869Gln
NM_004021.2:c.2606T>A NP_004012.1:p.Leu869Gln
NM_004022.2:c.2606T>A NP_004013.1:p.Leu869Gln
NM_004023.2:c.2606T>A NP_004014.1:p.Leu869Gln
XM_006724468.2:c.9986T>A XP_006724531.1:p.Leu3329Gln
XM_006724469.2:c.9962T>A XP_006724532.1:p.Leu3321Gln
XM_006724470.2:c.9986T>A XP_006724533.1:p.Leu3329Gln
XM_006724471.2:c.9986T>A XP_006724534.1:p.Leu3329Gln
XM_006724472.2:c.9857T>A XP_006724535.1:p.Leu3286Gln
XM_006724473.2:c.9848T>A XP_006724536.1:p.Leu3283Gln
XM_006724474.2:c.9986T>A XP_006724537.1:p.Leu3329Gln
XM_006724475.2:c.9986T>A XP_006724538.1:p.Leu3329Gln
XM_011545467.1:c.9863T>A XP_011543769.1:p.Leu3288Gln
XM_006724469.3:c.9962T>A XP_006724532.1:p.Leu3321Gln
XM_006724470.3:c.9986T>A XP_006724533.1:p.Leu3329Gln
XM_006724474.3:c.9986T>A XP_006724537.1:p.Leu3329Gln
XM_017029328.1:c.9986T>A XP_016884817.1:p.Leu3329Gln
XM_017029331.1:c.4160T>A XP_016884820.1:p.Leu1387Gln
NM_000109.4:c.9962T>A NP_000100.3:p.Leu3321Gln
NM_004006.3:c.9986T>A MANE Select NP_003997.2:p.Leu3329Gln
NM_004011.4:c.5963T>A NP_004002.3:p.Leu1988Gln
NM_004012.4:c.5954T>A NP_004003.2:p.Leu1985Gln
NM_004015.3:c.782T>A NP_004006.1:p.Leu261Gln
NM_004016.3:c.782T>A NP_004007.1:p.Leu261Gln
NM_004017.3:c.782T>A NP_004008.1:p.Leu261Gln
NM_004018.3:c.782T>A NP_004009.1:p.Leu261Gln
NM_004019.3:c.782T>A NP_004010.1:p.Leu261Gln
NM_004021.3:c.2606T>A NP_004012.2:p.Leu869Gln
NM_004023.3:c.2606T>A NP_004014.2:p.Leu869Gln
NM_004013.3:c.2606T>A NP_004004.2:p.Leu869Gln
NM_004014.3:c.1799T>A NP_004005.2:p.Leu600Gln
NM_004020.4:c.2606T>A NP_004011.3:p.Leu869Gln
NM_004022.3:c.2606T>A NP_004013.2:p.Leu869Gln