Canonical Allele Identifier: CA2499226669
Gene: DMD HGNC NCBI

Linked Data

dbSNP Id: rs796065325

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.33211299del , CM000685.2:g.33211299del GRCh38
NC_000023.10:g.33229416del , CM000685.1:g.33229416del GRCh37
NC_000023.9:g.33139337del NCBI36
NG_012232.1:g.133312del , LRG_199:g.133312del

Transcript Alleles

HGVS Amino-acid change
ENST00000463609.2:n.199del
ENST00000682071.1:c.-517del ENSP00000508133.1:n.-517del
ENST00000682307.1:n.199del
ENST00000682437.1:n.199del
ENST00000682439.1:n.199del
ENST00000682584.1:n.199del
ENST00000682870.1:n.200del
ENST00000682899.1:n.222del
ENST00000682924.1:c.15del ENSP00000508187.1:p.Glu6LysfsTer2
ENST00000683309.1:n.199del
ENST00000683658.1:n.198del
ENST00000683985.1:n.222del
ENST00000684056.1:n.199del
ENST00000684165.1:n.222del
ENST00000684237.1:c.15del ENSP00000507277.1:p.Glu6LysfsTer2
ENST00000684292.1:n.222del
ENST00000684357.1:n.199del
ENST00000684660.1:n.200del
ENST00000288447.9:c.7+127961del ENSP00000288447.4:n.7+127961del
ENST00000357033.9:c.15del MANE Select ENSP00000354923.3:p.Glu6LysfsTer2
ENST00000288447.8:c.7+127961del ENSP00000288447.4:n.7+127961del
ENST00000357033.8:c.15del ENSP00000354923.3:p.Glu6LysfsTer2
ENST00000420596.5:c.15del ENSP00000399897.1:p.Glu6LysfsTer2
ENST00000448370.5:c.15del ENSP00000388559.1:p.Glu6LysfsTer2
ENST00000463609.1:n.135del
ENST00000488902.5:n.257del
ENST00000620040.4:c.15del ENSP00000478150.1:p.Glu6LysfsTer2
NM_000109.3:c.7+127961del NP_000100.2:n.7+127961del
NM_004006.2:c.15del , LRG_199t1:c.15del NP_003997.1:p.Glu6LysfsTer2
XM_006724468.2:c.15del XP_006724531.1:p.Glu6LysfsTer2
XM_006724469.2:c.7+127961del XP_006724532.1:n.7+127961del
XM_006724470.2:c.15del XP_006724533.1:p.Glu6LysfsTer2
XM_006724471.2:c.15del XP_006724534.1:p.Glu6LysfsTer2
XM_006724472.2:c.15del XP_006724535.1:p.Glu6LysfsTer2
XM_006724473.2:c.15del XP_006724536.1:p.Glu6LysfsTer2
XM_006724474.2:c.15del XP_006724537.1:p.Glu6LysfsTer2
XM_006724475.2:c.15del XP_006724538.1:p.Glu6LysfsTer2
XM_011545467.1:c.15del XP_011543769.1:p.Glu6LysfsTer2
XM_011545468.1:c.15del XP_011543770.1:p.Glu6LysfsTer2
XM_011545469.1:c.15del XP_011543771.1:p.Glu6LysfsTer2
XM_006724469.3:c.7+127961del XP_006724532.1:n.7+127961del
XM_006724470.3:c.15del XP_006724533.1:p.Glu6LysfsTer2
XM_006724474.3:c.15del XP_006724537.1:p.Glu6LysfsTer2
XM_011545468.2:c.15del XP_011543770.1:p.Glu6LysfsTer2
XM_017029328.1:c.15del XP_016884817.1:p.Glu6LysfsTer2
XM_017029329.1:c.15del XP_016884818.1:p.Glu6LysfsTer2
XM_017029330.2:c.15del XP_016884819.1:p.Glu6LysfsTer2
NM_000109.4:c.7+127961del NP_000100.3:n.7+127961del
NM_004006.3:c.15del MANE Select NP_003997.2:p.Glu6LysfsTer2