Canonical Allele Identifier: CA2559535655
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32697896_32697901del , CM000685.2:g.32697896_32697901del GRCh38
NC_000023.10:g.32716013_32716018del , CM000685.1:g.32716013_32716018del GRCh37
NC_000023.9:g.32625934_32625939del NCBI36
NG_012232.1:g.646711_646716del , LRG_199:g.646711_646716del

Transcript Alleles

HGVS Amino-acid change
ENST00000682071.1:c.562_567del ENSP00000508133.1:p.Asp188_Pro189del
ENST00000682870.1:n.1116_1121del
ENST00000682899.1:n.1138_1143del
ENST00000682924.1:c.931_936del ENSP00000508187.1:p.Asp311_Pro312del
ENST00000683985.1:n.1138_1143del
ENST00000684165.1:n.1138_1143del
ENST00000684237.1:c.831+1213_831+1218del ENSP00000507277.1:n.831+1213_831+1218del
ENST00000684292.1:n.1138_1143del
ENST00000288447.9:c.907_912del ENSP00000288447.4:p.Asp303_Pro304del
ENST00000357033.9:c.931_936del MANE Select ENSP00000354923.3:p.Asp311_Pro312del
ENST00000288447.8:c.907_912del ENSP00000288447.4:p.Asp303_Pro304del
ENST00000357033.8:c.931_936del ENSP00000354923.3:p.Asp311_Pro312del
ENST00000378677.6:c.919_924del ENSP00000367948.2:p.Asp307_Pro308del
ENST00000420596.5:c.93+322240_93+322245del ENSP00000399897.1:n.93+322240_93+322245de...
ENST00000447523.1:c.247-124053_247-124048del ENSP00000395904.1:n.247-124053_247-124048...
ENST00000448370.5:c.93+322240_93+322245del ENSP00000388559.1:n.93+322240_93+322245de...
ENST00000480751.1:n.86+118569_86+118574del
ENST00000488902.5:n.335+322240_335+322245del
ENST00000619831.4:c.919_924del ENSP00000479270.1:p.Asp307_Pro308del
ENST00000620040.4:c.931_936del ENSP00000478150.1:p.Asp311_Pro312del
NM_000109.3:c.907_912del NP_000100.2:p.Asp303_Pro304del
NM_004006.2:c.931_936del , LRG_199t1:c.931_936del NP_003997.1:p.Asp311_Pro312del
NM_004009.3:c.919_924del NP_004000.1:p.Asp307_Pro308del
NM_004010.3:c.562_567del NP_004001.1:p.Asp188_Pro189del
XM_006724468.2:c.931_936del XP_006724531.1:p.Asp311_Pro312del
XM_006724469.2:c.907_912del XP_006724532.1:p.Asp303_Pro304del
XM_006724470.2:c.931_936del XP_006724533.1:p.Asp311_Pro312del
XM_006724471.2:c.931_936del XP_006724534.1:p.Asp311_Pro312del
XM_006724472.2:c.831+1213_831+1218del XP_006724535.1:n.831+1213_831+1218del
XM_006724473.2:c.931_936del XP_006724536.1:p.Asp311_Pro312del
XM_006724474.2:c.931_936del XP_006724537.1:p.Asp311_Pro312del
XM_006724475.2:c.931_936del XP_006724538.1:p.Asp311_Pro312del
XM_011545467.1:c.931_936del XP_011543769.1:p.Asp311_Pro312del
XM_011545468.1:c.931_936del XP_011543770.1:p.Asp311_Pro312del
XM_011545469.1:c.931_936del XP_011543771.1:p.Asp311_Pro312del
XM_006724469.3:c.907_912del XP_006724532.1:p.Asp303_Pro304del
XM_006724470.3:c.931_936del XP_006724533.1:p.Asp311_Pro312del
XM_006724474.3:c.931_936del XP_006724537.1:p.Asp311_Pro312del
XM_011545468.2:c.931_936del XP_011543770.1:p.Asp311_Pro312del
XM_017029328.1:c.931_936del XP_016884817.1:p.Asp311_Pro312del
XM_017029329.1:c.931_936del XP_016884818.1:p.Asp311_Pro312del
XM_017029330.2:c.931_936del XP_016884819.1:p.Asp311_Pro312del
NM_000109.4:c.907_912del NP_000100.3:p.Asp303_Pro304del
NM_004006.3:c.931_936del MANE Select NP_003997.2:p.Asp311_Pro312del