Canonical Allele Identifier: CA10377848
Gene: DMD HGNC NCBI

Linked Data

dbSNP Id: rs770906691
gnomAD v2: X-31279075-A-T
gnomAD v4: X-31260958-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.31260958A>T , CM000685.2:g.31260958A>T GRCh38
NC_000023.10:g.31279075A>T , CM000685.1:g.31279075A>T GRCh37
NC_000023.9:g.31188996A>T NCBI36
NG_012232.1:g.2083652T>A , LRG_199:g.2083652T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000358062.7:c.4129T>A ENSP00000350765.3:p.Leu1377Ile
ENST00000680162.2:c.79T>A ENSP00000506634.2:p.Leu27Ile
ENST00000680768.2:c.79T>A ENSP00000506359.2:p.Leu27Ile
ENST00000682238.1:c.1903T>A ENSP00000508124.1:p.Leu635Ile
ENST00000682322.1:c.79T>A ENSP00000507690.1:p.Leu27Ile
ENST00000682600.1:c.79T>A ENSP00000507640.1:p.Leu27Ile
ENST00000683509.1:n.800T>A
ENST00000683675.1:n.382T>A
ENST00000683709.1:n.801T>A
ENST00000683957.1:n.2775T>A
ENST00000684130.1:c.1903T>A ENSP00000508037.1:p.Leu635Ile
ENST00000343523.7:c.1138T>A ENSP00000340057.4:p.Leu380Ile
ENST00000357033.9:c.9283T>A MANE Select ENSP00000354923.3:p.Leu3095Ile
ENST00000619831.5:c.5251T>A ENSP00000479270.2:p.Leu1751Ile
ENST00000620040.5:c.1903T>A ENSP00000478150.2:p.Leu635Ile
ENST00000679641.1:c.79T>A ENSP00000506135.1:p.Leu27Ile
ENST00000680216.1:c.59T>A
ENST00000680355.1:c.79T>A ENSP00000506257.1:p.Leu27Ile
ENST00000680557.1:c.79T>A ENSP00000505164.1:p.Leu27Ile
ENST00000680768.1:c.22T>A ENSP00000506359.1:p.Leu8Ile
ENST00000680961.1:c.1903T>A ENSP00000506386.1:p.Leu635Ile
ENST00000681153.1:c.79T>A ENSP00000505124.1:p.Leu27Ile
ENST00000681334.1:c.79T>A ENSP00000506066.1:p.Leu27Ile
ENST00000681646.1:n.2944T>A
ENST00000681654.1:n.213T>A
ENST00000681870.1:c.79T>A ENSP00000506709.1:p.Leu27Ile
ENST00000343523.6:c.1096T>A ENSP00000340057.3:p.Leu366Ile
ENST00000357033.8:c.9283T>A ENSP00000354923.3:p.Leu3095Ile
ENST00000358062.6:c.2371T>A ENSP00000350765.2:p.Leu791Ile
ENST00000359836.5:c.1903T>A ENSP00000352894.1:p.Leu635Ile
ENST00000361471.8:c.79T>A ENSP00000354464.4:p.Leu27Ile
ENST00000378677.6:c.9271T>A ENSP00000367948.2:p.Leu3091Ile
ENST00000378680.6:c.79T>A ENSP00000367951.2:p.Leu27Ile
ENST00000378702.8:c.79T>A ENSP00000367974.4:p.Leu27Ile
ENST00000378707.7:c.1903T>A ENSP00000367979.3:p.Leu635Ile
ENST00000378723.7:c.79T>A ENSP00000367997.3:p.Leu27Ile
ENST00000469142.1:n.302T>A
ENST00000474231.5:c.1903T>A ENSP00000417123.1:p.Leu635Ile
ENST00000541735.5:c.1903T>A ENSP00000444119.1:p.Leu635Ile
ENST00000619831.4:c.9268T>A ENSP00000479270.1:p.Leu3090Ile
ENST00000620040.4:c.9280T>A ENSP00000478150.1:p.Leu3094Ile
NM_000109.3:c.9259T>A NP_000100.2:p.Leu3087Ile
NM_004006.2:c.9283T>A , LRG_199t1:c.9283T>A NP_003997.1:p.Leu3095Ile
NM_004009.3:c.9271T>A NP_004000.1:p.Leu3091Ile
NM_004010.3:c.8914T>A NP_004001.1:p.Leu2972Ile
NM_004011.3:c.5260T>A NP_004002.2:p.Leu1754Ile
NM_004012.3:c.5251T>A NP_004003.1:p.Leu1751Ile
NM_004013.2:c.1903T>A NP_004004.1:p.Leu635Ile
NM_004014.2:c.1096T>A NP_004005.1:p.Leu366Ile
NM_004015.2:c.79T>A NP_004006.1:p.Leu27Ile
NM_004016.2:c.79T>A NP_004007.1:p.Leu27Ile
NM_004017.2:c.79T>A NP_004008.1:p.Leu27Ile
NM_004018.2:c.79T>A NP_004009.1:p.Leu27Ile
NM_004019.2:c.79T>A NP_004010.1:p.Leu27Ile
NM_004020.3:c.1903T>A NP_004011.2:p.Leu635Ile
NM_004021.2:c.1903T>A NP_004012.1:p.Leu635Ile
NM_004022.2:c.1903T>A NP_004013.1:p.Leu635Ile
NM_004023.2:c.1903T>A NP_004014.1:p.Leu635Ile
XM_006724468.2:c.9283T>A XP_006724531.1:p.Leu3095Ile
XM_006724469.2:c.9259T>A XP_006724532.1:p.Leu3087Ile
XM_006724470.2:c.9283T>A XP_006724533.1:p.Leu3095Ile
XM_006724471.2:c.9283T>A XP_006724534.1:p.Leu3095Ile
XM_006724472.2:c.9154T>A XP_006724535.1:p.Leu3052Ile
XM_006724473.2:c.9145T>A XP_006724536.1:p.Leu3049Ile
XM_006724474.2:c.9283T>A XP_006724537.1:p.Leu3095Ile
XM_006724475.2:c.9283T>A XP_006724538.1:p.Leu3095Ile
XM_011545467.1:c.9160T>A XP_011543769.1:p.Leu3054Ile
XM_011545468.1:c.9283T>A XP_011543770.1:p.Leu3095Ile
XM_006724469.3:c.9259T>A XP_006724532.1:p.Leu3087Ile
XM_006724470.3:c.9283T>A XP_006724533.1:p.Leu3095Ile
XM_006724474.3:c.9283T>A XP_006724537.1:p.Leu3095Ile
XM_011545468.2:c.9283T>A XP_011543770.1:p.Leu3095Ile
XM_017029328.1:c.9283T>A XP_016884817.1:p.Leu3095Ile
XM_017029331.1:c.3457T>A XP_016884820.1:p.Leu1153Ile
NM_000109.4:c.9259T>A NP_000100.3:p.Leu3087Ile
NM_004006.3:c.9283T>A MANE Select NP_003997.2:p.Leu3095Ile
NM_004011.4:c.5260T>A NP_004002.3:p.Leu1754Ile
NM_004012.4:c.5251T>A NP_004003.2:p.Leu1751Ile
NM_004015.3:c.79T>A NP_004006.1:p.Leu27Ile
NM_004016.3:c.79T>A NP_004007.1:p.Leu27Ile
NM_004017.3:c.79T>A NP_004008.1:p.Leu27Ile
NM_004018.3:c.79T>A NP_004009.1:p.Leu27Ile
NM_004019.3:c.79T>A NP_004010.1:p.Leu27Ile
NM_004021.3:c.1903T>A NP_004012.2:p.Leu635Ile
NM_004023.3:c.1903T>A NP_004014.2:p.Leu635Ile
NM_004013.3:c.1903T>A NP_004004.2:p.Leu635Ile
NM_004014.3:c.1096T>A NP_004005.2:p.Leu366Ile
NM_004020.4:c.1903T>A NP_004011.3:p.Leu635Ile
NM_004022.3:c.1903T>A NP_004013.2:p.Leu635Ile