Canonical Allele Identifier: CA2534609456
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32697900_32697902del , CM000685.2:g.32697900_32697902del GRCh38
NC_000023.10:g.32716017_32716019del , CM000685.1:g.32716017_32716019del GRCh37
NC_000023.9:g.32625938_32625940del NCBI36
NG_012232.1:g.646708_646710del , LRG_199:g.646708_646710del

Transcript Alleles

HGVS Amino-acid change
ENST00000682071.1:c.559_561del ENSP00000508133.1:p.Ser187del
ENST00000682870.1:n.1113_1115del
ENST00000682899.1:n.1135_1137del
ENST00000682924.1:c.928_930del ENSP00000508187.1:p.Ser310del
ENST00000683985.1:n.1135_1137del
ENST00000684165.1:n.1135_1137del
ENST00000684237.1:c.831+1210_831+1212del ENSP00000507277.1:n.831+1210_831+1212del
ENST00000684292.1:n.1135_1137del
ENST00000288447.9:c.904_906del ENSP00000288447.4:p.Ser302del
ENST00000357033.9:c.928_930del MANE Select ENSP00000354923.3:p.Ser310del
ENST00000288447.8:c.904_906del ENSP00000288447.4:p.Ser302del
ENST00000357033.8:c.928_930del ENSP00000354923.3:p.Ser310del
ENST00000378677.6:c.916_918del ENSP00000367948.2:p.Ser306del
ENST00000420596.5:c.93+322237_93+322239del ENSP00000399897.1:n.93+322237_93+322239de...
ENST00000447523.1:c.247-124056_247-124054del ENSP00000395904.1:n.247-124056_247-124054...
ENST00000448370.5:c.93+322237_93+322239del ENSP00000388559.1:n.93+322237_93+322239de...
ENST00000480751.1:n.86+118566_86+118568del
ENST00000488902.5:n.335+322237_335+322239del
ENST00000619831.4:c.916_918del ENSP00000479270.1:p.Ser306del
ENST00000620040.4:c.928_930del ENSP00000478150.1:p.Ser310del
NM_000109.3:c.904_906del NP_000100.2:p.Ser302del
NM_004006.2:c.928_930del , LRG_199t1:c.928_930del NP_003997.1:p.Ser310del
NM_004009.3:c.916_918del NP_004000.1:p.Ser306del
NM_004010.3:c.559_561del NP_004001.1:p.Ser187del
XM_006724468.2:c.928_930del XP_006724531.1:p.Ser310del
XM_006724469.2:c.904_906del XP_006724532.1:p.Ser302del
XM_006724470.2:c.928_930del XP_006724533.1:p.Ser310del
XM_006724471.2:c.928_930del XP_006724534.1:p.Ser310del
XM_006724472.2:c.831+1210_831+1212del XP_006724535.1:n.831+1210_831+1212del
XM_006724473.2:c.928_930del XP_006724536.1:p.Ser310del
XM_006724474.2:c.928_930del XP_006724537.1:p.Ser310del
XM_006724475.2:c.928_930del XP_006724538.1:p.Ser310del
XM_011545467.1:c.928_930del XP_011543769.1:p.Ser310del
XM_011545468.1:c.928_930del XP_011543770.1:p.Ser310del
XM_011545469.1:c.928_930del XP_011543771.1:p.Ser310del
XM_006724469.3:c.904_906del XP_006724532.1:p.Ser302del
XM_006724470.3:c.928_930del XP_006724533.1:p.Ser310del
XM_006724474.3:c.928_930del XP_006724537.1:p.Ser310del
XM_011545468.2:c.928_930del XP_011543770.1:p.Ser310del
XM_017029328.1:c.928_930del XP_016884817.1:p.Ser310del
XM_017029329.1:c.928_930del XP_016884818.1:p.Ser310del
XM_017029330.2:c.928_930del XP_016884819.1:p.Ser310del
NM_000109.4:c.904_906del NP_000100.3:p.Ser302del
NM_004006.3:c.928_930del MANE Select NP_003997.2:p.Ser310del