Canonical Allele Identifier: CA328458499
Gene: DMD HGNC NCBI

Linked Data

dbSNP Id: rs752054832

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.31627411del , CM000685.2:g.31627411del GRCh38
NC_000023.10:g.31645528del , CM000685.1:g.31645528del GRCh37
NC_000023.9:g.31555449del NCBI36
NG_012232.1:g.1717200del , LRG_199:g.1717200del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358062.7:c.3063+263del ENSP00000350765.3:n.3063+263del
ENST00000682238.1:c.837+263del ENSP00000508124.1:n.837+263del
ENST00000683450.1:n.1682+263del
ENST00000683851.1:n.2141del
ENST00000683957.1:n.1709+263del
ENST00000684130.1:c.837+263del ENSP00000508037.1:n.837+263del
ENST00000357033.9:c.8217+263del MANE Select ENSP00000354923.3:n.8217+263del
ENST00000619831.5:c.4185+263del ENSP00000479270.2:n.4185+263del
ENST00000620040.5:c.837+263del ENSP00000478150.2:n.837+263del
ENST00000680961.1:c.837+263del ENSP00000506386.1:n.837+263del
ENST00000681646.1:n.1878+263del
ENST00000357033.8:c.8217+263del ENSP00000354923.3:n.8217+263del
ENST00000358062.6:c.1305+263del ENSP00000350765.2:n.1305+263del
ENST00000359836.5:c.837+263del ENSP00000352894.1:n.837+263del
ENST00000378677.6:c.8205+263del ENSP00000367948.2:n.8205+263del
ENST00000378707.7:c.837+263del ENSP00000367979.3:n.837+263del
ENST00000474231.5:c.837+263del ENSP00000417123.1:n.837+263del
ENST00000541735.5:c.837+263del ENSP00000444119.1:n.837+263del
ENST00000619831.4:c.8202+263del ENSP00000479270.1:n.8202+263del
ENST00000620040.4:c.8214+263del ENSP00000478150.1:n.8214+263del
NM_000109.3:c.8193+263del NP_000100.2:n.8193+263del
NM_004006.2:c.8217+263del , LRG_199t1:c.8217+263del NP_003997.1:n.8217+263del
NM_004009.3:c.8205+263del NP_004000.1:n.8205+263del
NM_004010.3:c.7848+263del NP_004001.1:n.7848+263del
NM_004011.3:c.4194+263del NP_004002.2:n.4194+263del
NM_004012.3:c.4185+263del NP_004003.1:n.4185+263del
NM_004013.2:c.837+263del NP_004004.1:n.837+263del
NM_004020.3:c.837+263del NP_004011.2:n.837+263del
NM_004021.2:c.837+263del NP_004012.1:n.837+263del
NM_004022.2:c.837+263del NP_004013.1:n.837+263del
NM_004023.2:c.837+263del NP_004014.1:n.837+263del
XM_006724468.2:c.8217+263del XP_006724531.1:n.8217+263del
XM_006724469.2:c.8193+263del XP_006724532.1:n.8193+263del
XM_006724470.2:c.8217+263del XP_006724533.1:n.8217+263del
XM_006724471.2:c.8217+263del XP_006724534.1:n.8217+263del
XM_006724472.2:c.8088+263del XP_006724535.1:n.8088+263del
XM_006724473.2:c.8079+263del XP_006724536.1:n.8079+263del
XM_006724474.2:c.8217+263del XP_006724537.1:n.8217+263del
XM_006724475.2:c.8217+263del XP_006724538.1:n.8217+263del
XM_011545467.1:c.8094+263del XP_011543769.1:n.8094+263del
XM_011545468.1:c.8217+263del XP_011543770.1:n.8217+263del
XM_006724469.3:c.8193+263del XP_006724532.1:n.8193+263del
XM_006724470.3:c.8217+263del XP_006724533.1:n.8217+263del
XM_006724474.3:c.8217+263del XP_006724537.1:n.8217+263del
XM_011545468.2:c.8217+263del XP_011543770.1:n.8217+263del
XM_017029328.1:c.8217+263del XP_016884817.1:n.8217+263del
XM_017029331.1:c.2391+263del XP_016884820.1:n.2391+263del
NM_000109.4:c.8193+263del NP_000100.3:n.8193+263del
NM_004006.3:c.8217+263del MANE Select NP_003997.2:n.8217+263del
NM_004011.4:c.4194+263del NP_004002.3:n.4194+263del
NM_004012.4:c.4185+263del NP_004003.2:n.4185+263del
NM_004021.3:c.837+263del NP_004012.2:n.837+263del
NM_004023.3:c.837+263del NP_004014.2:n.837+263del
NM_004013.3:c.837+263del NP_004004.2:n.837+263del
NM_004020.4:c.837+263del NP_004011.3:n.837+263del
NM_004022.3:c.837+263del NP_004013.2:n.837+263del