Canonical Allele Identifier: CA412652710
Gene: DMD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.31178687T>C , CM000685.2:g.31178687T>C GRCh38
NC_000023.10:g.31196804T>C , CM000685.1:g.31196804T>C GRCh37
NC_000023.9:g.31106725T>C NCBI36
NG_012232.1:g.2165923A>G , LRG_199:g.2165923A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358062.7:c.5051A>G ENSP00000350765.3:p.Glu1684Gly
ENST00000475732.3:n.2552A>G
ENST00000680162.2:c.1001A>G ENSP00000506634.2:p.Glu334Gly
ENST00000680768.2:c.1001A>G ENSP00000506359.2:p.Glu334Gly
ENST00000681989.1:n.1003A>G
ENST00000682238.1:c.2825A>G ENSP00000508124.1:p.Glu942Gly
ENST00000682322.1:c.1001A>G ENSP00000507690.1:p.Glu334Gly
ENST00000682600.1:c.1001A>G ENSP00000507640.1:p.Glu334Gly
ENST00000682769.1:n.836A>G
ENST00000683509.1:n.1722A>G
ENST00000683675.1:n.1304A>G
ENST00000683709.1:n.1723A>G
ENST00000683957.1:n.3697A>G
ENST00000684130.1:c.2825A>G ENSP00000508037.1:p.Glu942Gly
ENST00000343523.7:c.2060A>G ENSP00000340057.4:p.Glu687Gly
ENST00000357033.9:c.10205A>G MANE Select ENSP00000354923.3:p.Glu3402Gly
ENST00000475732.2:n.571A>G
ENST00000619831.5:c.6173A>G ENSP00000479270.2:p.Glu2058Gly
ENST00000620040.5:c.2825A>G ENSP00000478150.2:p.Glu942Gly
ENST00000679641.1:c.*207A>G ENSP00000506135.1:n.*207A>G
ENST00000679706.1:c.162A>G
ENST00000680162.1:c.878A>G ENSP00000506634.1:p.Glu293Gly
ENST00000680355.1:c.1001A>G ENSP00000506257.1:p.Glu334Gly
ENST00000680557.1:c.603+25274A>G ENSP00000505164.1:n.603+25274A>G
ENST00000680768.1:c.944A>G ENSP00000506359.1:p.Glu315Gly
ENST00000680961.1:c.*207A>G ENSP00000506386.1:n.*207A>G
ENST00000681153.1:c.1001A>G ENSP00000505124.1:p.Glu334Gly
ENST00000681654.1:n.1135A>G
ENST00000343523.6:c.2018A>G ENSP00000340057.3:p.Glu673Gly
ENST00000357033.8:c.10205A>G ENSP00000354923.3:p.Glu3402Gly
ENST00000358062.6:c.3293A>G ENSP00000350765.2:p.Glu1098Gly
ENST00000359836.5:c.2825A>G ENSP00000352894.1:p.Glu942Gly
ENST00000361471.8:c.1001A>G ENSP00000354464.4:p.Glu334Gly
ENST00000378677.6:c.10193A>G ENSP00000367948.2:p.Glu3398Gly
ENST00000378680.6:c.1001A>G ENSP00000367951.2:p.Glu334Gly
ENST00000378702.8:c.1001A>G ENSP00000367974.4:p.Glu334Gly
ENST00000378705.3:c.575A>G ENSP00000367977.3:p.Glu192Gly
ENST00000378707.7:c.2825A>G ENSP00000367979.3:p.Glu942Gly
ENST00000378723.7:c.1001A>G ENSP00000367997.3:p.Glu334Gly
ENST00000474231.5:c.2825A>G ENSP00000417123.1:p.Glu942Gly
ENST00000475732.1:n.421A>G
ENST00000541735.5:c.2825A>G ENSP00000444119.1:p.Glu942Gly
ENST00000619831.4:c.10190A>G ENSP00000479270.1:p.Glu3397Gly
ENST00000620040.4:c.10202A>G ENSP00000478150.1:p.Glu3401Gly
NM_000109.3:c.10181A>G NP_000100.2:p.Glu3394Gly
NM_004006.2:c.10205A>G , LRG_199t1:c.10205A>G NP_003997.1:p.Glu3402Gly
NM_004009.3:c.10193A>G NP_004000.1:p.Glu3398Gly
NM_004010.3:c.9836A>G NP_004001.1:p.Glu3279Gly
NM_004011.3:c.6182A>G NP_004002.2:p.Glu2061Gly
NM_004012.3:c.6173A>G NP_004003.1:p.Glu2058Gly
NM_004013.2:c.2825A>G NP_004004.1:p.Glu942Gly
NM_004014.2:c.2018A>G NP_004005.1:p.Glu673Gly
NM_004015.2:c.1001A>G NP_004006.1:p.Glu334Gly
NM_004016.2:c.1001A>G NP_004007.1:p.Glu334Gly
NM_004017.2:c.1001A>G NP_004008.1:p.Glu334Gly
NM_004018.2:c.1001A>G NP_004009.1:p.Glu334Gly
NM_004019.2:c.1001A>G NP_004010.1:p.Glu334Gly
NM_004020.3:c.2825A>G NP_004011.2:p.Glu942Gly
NM_004021.2:c.2825A>G NP_004012.1:p.Glu942Gly
NM_004022.2:c.2825A>G NP_004013.1:p.Glu942Gly
NM_004023.2:c.2825A>G NP_004014.1:p.Glu942Gly
XM_006724468.2:c.10205A>G XP_006724531.1:p.Glu3402Gly
XM_006724469.2:c.10181A>G XP_006724532.1:p.Glu3394Gly
XM_006724470.2:c.10205A>G XP_006724533.1:p.Glu3402Gly
XM_006724471.2:c.10205A>G XP_006724534.1:p.Glu3402Gly
XM_006724472.2:c.10076A>G XP_006724535.1:p.Glu3359Gly
XM_006724473.2:c.10067A>G XP_006724536.1:p.Glu3356Gly
XM_006724474.2:c.10205A>G XP_006724537.1:p.Glu3402Gly
XM_006724475.2:c.10205A>G XP_006724538.1:p.Glu3402Gly
XM_011545467.1:c.10082A>G XP_011543769.1:p.Glu3361Gly
XM_006724469.3:c.10181A>G XP_006724532.1:p.Glu3394Gly
XM_006724470.3:c.10205A>G XP_006724533.1:p.Glu3402Gly
XM_006724474.3:c.10205A>G XP_006724537.1:p.Glu3402Gly
XM_017029328.1:c.10205A>G XP_016884817.1:p.Glu3402Gly
XM_017029331.1:c.4379A>G XP_016884820.1:p.Glu1460Gly
NM_000109.4:c.10181A>G NP_000100.3:p.Glu3394Gly
NM_004006.3:c.10205A>G MANE Select NP_003997.2:p.Glu3402Gly
NM_004011.4:c.6182A>G NP_004002.3:p.Glu2061Gly
NM_004012.4:c.6173A>G NP_004003.2:p.Glu2058Gly
NM_004015.3:c.1001A>G NP_004006.1:p.Glu334Gly
NM_004016.3:c.1001A>G NP_004007.1:p.Glu334Gly
NM_004017.3:c.1001A>G NP_004008.1:p.Glu334Gly
NM_004018.3:c.1001A>G NP_004009.1:p.Glu334Gly
NM_004019.3:c.1001A>G NP_004010.1:p.Glu334Gly
NM_004021.3:c.2825A>G NP_004012.2:p.Glu942Gly
NM_004023.3:c.2825A>G NP_004014.2:p.Glu942Gly
NM_004013.3:c.2825A>G NP_004004.2:p.Glu942Gly
NM_004014.3:c.2018A>G NP_004005.2:p.Glu673Gly
NM_004020.4:c.2825A>G NP_004011.3:p.Glu942Gly
NM_004022.3:c.2825A>G NP_004013.2:p.Glu942Gly