Canonical Allele Identifier: CA412652453
Gene: DMD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.31260967A>G , CM000685.2:g.31260967A>G GRCh38
NC_000023.10:g.31279084A>G , CM000685.1:g.31279084A>G GRCh37
NC_000023.9:g.31189005A>G NCBI36
NG_012232.1:g.2083643T>C , LRG_199:g.2083643T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358062.7:c.4120T>C ENSP00000350765.3:p.Tyr1374His
ENST00000680162.2:c.70T>C ENSP00000506634.2:p.Tyr24His
ENST00000680768.2:c.70T>C ENSP00000506359.2:p.Tyr24His
ENST00000682238.1:c.1894T>C ENSP00000508124.1:p.Tyr632His
ENST00000682322.1:c.70T>C ENSP00000507690.1:p.Tyr24His
ENST00000682600.1:c.70T>C ENSP00000507640.1:p.Tyr24His
ENST00000683509.1:n.791T>C
ENST00000683675.1:n.373T>C
ENST00000683709.1:n.792T>C
ENST00000683957.1:n.2766T>C
ENST00000684130.1:c.1894T>C ENSP00000508037.1:p.Tyr632His
ENST00000343523.7:c.1129T>C ENSP00000340057.4:p.Tyr377His
ENST00000357033.9:c.9274T>C MANE Select ENSP00000354923.3:p.Tyr3092His
ENST00000619831.5:c.5242T>C ENSP00000479270.2:p.Tyr1748His
ENST00000620040.5:c.1894T>C ENSP00000478150.2:p.Tyr632His
ENST00000679641.1:c.70T>C ENSP00000506135.1:p.Tyr24His
ENST00000680216.1:c.50T>C
ENST00000680355.1:c.70T>C ENSP00000506257.1:p.Tyr24His
ENST00000680557.1:c.70T>C ENSP00000505164.1:p.Tyr24His
ENST00000680768.1:c.13T>C ENSP00000506359.1:p.Tyr5His
ENST00000680961.1:c.1894T>C ENSP00000506386.1:p.Tyr632His
ENST00000681153.1:c.70T>C ENSP00000505124.1:p.Tyr24His
ENST00000681334.1:c.70T>C ENSP00000506066.1:p.Tyr24His
ENST00000681646.1:n.2935T>C
ENST00000681654.1:n.204T>C
ENST00000681870.1:c.70T>C ENSP00000506709.1:p.Tyr24His
ENST00000343523.6:c.1087T>C ENSP00000340057.3:p.Tyr363His
ENST00000357033.8:c.9274T>C ENSP00000354923.3:p.Tyr3092His
ENST00000358062.6:c.2362T>C ENSP00000350765.2:p.Tyr788His
ENST00000359836.5:c.1894T>C ENSP00000352894.1:p.Tyr632His
ENST00000361471.8:c.70T>C ENSP00000354464.4:p.Tyr24His
ENST00000378677.6:c.9262T>C ENSP00000367948.2:p.Tyr3088His
ENST00000378680.6:c.70T>C ENSP00000367951.2:p.Tyr24His
ENST00000378702.8:c.70T>C ENSP00000367974.4:p.Tyr24His
ENST00000378707.7:c.1894T>C ENSP00000367979.3:p.Tyr632His
ENST00000378723.7:c.70T>C ENSP00000367997.3:p.Tyr24His
ENST00000469142.1:n.293T>C
ENST00000474231.5:c.1894T>C ENSP00000417123.1:p.Tyr632His
ENST00000541735.5:c.1894T>C ENSP00000444119.1:p.Tyr632His
ENST00000619831.4:c.9259T>C ENSP00000479270.1:p.Tyr3087His
ENST00000620040.4:c.9271T>C ENSP00000478150.1:p.Tyr3091His
NM_000109.3:c.9250T>C NP_000100.2:p.Tyr3084His
NM_004006.2:c.9274T>C , LRG_199t1:c.9274T>C NP_003997.1:p.Tyr3092His
NM_004009.3:c.9262T>C NP_004000.1:p.Tyr3088His
NM_004010.3:c.8905T>C NP_004001.1:p.Tyr2969His
NM_004011.3:c.5251T>C NP_004002.2:p.Tyr1751His
NM_004012.3:c.5242T>C NP_004003.1:p.Tyr1748His
NM_004013.2:c.1894T>C NP_004004.1:p.Tyr632His
NM_004014.2:c.1087T>C NP_004005.1:p.Tyr363His
NM_004015.2:c.70T>C NP_004006.1:p.Tyr24His
NM_004016.2:c.70T>C NP_004007.1:p.Tyr24His
NM_004017.2:c.70T>C NP_004008.1:p.Tyr24His
NM_004018.2:c.70T>C NP_004009.1:p.Tyr24His
NM_004019.2:c.70T>C NP_004010.1:p.Tyr24His
NM_004020.3:c.1894T>C NP_004011.2:p.Tyr632His
NM_004021.2:c.1894T>C NP_004012.1:p.Tyr632His
NM_004022.2:c.1894T>C NP_004013.1:p.Tyr632His
NM_004023.2:c.1894T>C NP_004014.1:p.Tyr632His
XM_006724468.2:c.9274T>C XP_006724531.1:p.Tyr3092His
XM_006724469.2:c.9250T>C XP_006724532.1:p.Tyr3084His
XM_006724470.2:c.9274T>C XP_006724533.1:p.Tyr3092His
XM_006724471.2:c.9274T>C XP_006724534.1:p.Tyr3092His
XM_006724472.2:c.9145T>C XP_006724535.1:p.Tyr3049His
XM_006724473.2:c.9136T>C XP_006724536.1:p.Tyr3046His
XM_006724474.2:c.9274T>C XP_006724537.1:p.Tyr3092His
XM_006724475.2:c.9274T>C XP_006724538.1:p.Tyr3092His
XM_011545467.1:c.9151T>C XP_011543769.1:p.Tyr3051His
XM_011545468.1:c.9274T>C XP_011543770.1:p.Tyr3092His
XM_006724469.3:c.9250T>C XP_006724532.1:p.Tyr3084His
XM_006724470.3:c.9274T>C XP_006724533.1:p.Tyr3092His
XM_006724474.3:c.9274T>C XP_006724537.1:p.Tyr3092His
XM_011545468.2:c.9274T>C XP_011543770.1:p.Tyr3092His
XM_017029328.1:c.9274T>C XP_016884817.1:p.Tyr3092His
XM_017029331.1:c.3448T>C XP_016884820.1:p.Tyr1150His
NM_000109.4:c.9250T>C NP_000100.3:p.Tyr3084His
NM_004006.3:c.9274T>C MANE Select NP_003997.2:p.Tyr3092His
NM_004011.4:c.5251T>C NP_004002.3:p.Tyr1751His
NM_004012.4:c.5242T>C NP_004003.2:p.Tyr1748His
NM_004015.3:c.70T>C NP_004006.1:p.Tyr24His
NM_004016.3:c.70T>C NP_004007.1:p.Tyr24His
NM_004017.3:c.70T>C NP_004008.1:p.Tyr24His
NM_004018.3:c.70T>C NP_004009.1:p.Tyr24His
NM_004019.3:c.70T>C NP_004010.1:p.Tyr24His
NM_004021.3:c.1894T>C NP_004012.2:p.Tyr632His
NM_004023.3:c.1894T>C NP_004014.2:p.Tyr632His
NM_004013.3:c.1894T>C NP_004004.2:p.Tyr632His
NM_004014.3:c.1087T>C NP_004005.2:p.Tyr363His
NM_004020.4:c.1894T>C NP_004011.3:p.Tyr632His
NM_004022.3:c.1894T>C NP_004013.2:p.Tyr632His