Canonical Allele Identifier: CA16043826
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.33020153dup , CM000685.2:g.33020153dup GRCh38
NC_000023.10:g.33038270dup , CM000685.1:g.33038270dup GRCh37
NC_000023.9:g.32948191dup NCBI36
NG_012232.1:g.324457dup , LRG_199:g.324457dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682071.1:c.-291dup ENSP00000508133.1:n.-291dup
ENST00000682307.1:n.263dup
ENST00000682437.1:n.263dup
ENST00000682439.1:n.263dup
ENST00000682584.1:n.263dup
ENST00000682870.1:n.264dup
ENST00000682899.1:n.286dup
ENST00000682924.1:c.79dup ENSP00000508187.1:p.Ala27GlyfsTer5
ENST00000683309.1:n.263dup
ENST00000683658.1:n.424dup
ENST00000683985.1:n.286dup
ENST00000684056.1:n.263dup
ENST00000684165.1:n.286dup
ENST00000684237.1:c.79dup ENSP00000507277.1:p.Ala27GlyfsTer5
ENST00000684292.1:n.286dup
ENST00000684357.1:n.263dup
ENST00000684660.1:n.264dup
ENST00000288447.9:c.55dup ENSP00000288447.4:p.Ala19GlyfsTer5
ENST00000357033.9:c.79dup MANE Select ENSP00000354923.3:p.Ala27GlyfsTer5
ENST00000288447.8:c.55dup ENSP00000288447.4:p.Ala19GlyfsTer5
ENST00000357033.8:c.79dup ENSP00000354923.3:p.Ala27GlyfsTer5
ENST00000378677.6:c.67dup ENSP00000367948.2:p.Ala23GlyfsTer5
ENST00000420596.5:c.79dup ENSP00000399897.1:p.Ala27GlyfsTer5
ENST00000448370.5:c.79dup ENSP00000388559.1:p.Ala27GlyfsTer5
ENST00000472681.1:n.124dup
ENST00000488902.5:n.321dup
ENST00000619831.4:c.67dup ENSP00000479270.1:p.Ala23GlyfsTer5
ENST00000620040.4:c.79dup ENSP00000478150.1:p.Ala27GlyfsTer5
NM_000109.3:c.55dup NP_000100.2:p.Ala19GlyfsTer5
NM_004006.2:c.79dup , LRG_199t1:c.79dup NP_003997.1:p.Ala27GlyfsTer5
NM_004009.3:c.67dup NP_004000.1:p.Ala23GlyfsTer5
NM_004010.3:c.-291dup NP_004001.1:n.-291dup
XM_006724468.2:c.79dup XP_006724531.1:p.Ala27GlyfsTer5
XM_006724469.2:c.55dup XP_006724532.1:p.Ala19GlyfsTer5
XM_006724470.2:c.79dup XP_006724533.1:p.Ala27GlyfsTer5
XM_006724471.2:c.79dup XP_006724534.1:p.Ala27GlyfsTer5
XM_006724472.2:c.79dup XP_006724535.1:p.Ala27GlyfsTer5
XM_006724473.2:c.79dup XP_006724536.1:p.Ala27GlyfsTer5
XM_006724474.2:c.79dup XP_006724537.1:p.Ala27GlyfsTer5
XM_006724475.2:c.79dup XP_006724538.1:p.Ala27GlyfsTer5
XM_011545467.1:c.79dup XP_011543769.1:p.Ala27GlyfsTer5
XM_011545468.1:c.79dup XP_011543770.1:p.Ala27GlyfsTer5
XM_011545469.1:c.79dup XP_011543771.1:p.Ala27GlyfsTer5
XM_006724469.3:c.55dup XP_006724532.1:p.Ala19GlyfsTer5
XM_006724470.3:c.79dup XP_006724533.1:p.Ala27GlyfsTer5
XM_006724474.3:c.79dup XP_006724537.1:p.Ala27GlyfsTer5
XM_011545468.2:c.79dup XP_011543770.1:p.Ala27GlyfsTer5
XM_017029328.1:c.79dup XP_016884817.1:p.Ala27GlyfsTer5
XM_017029329.1:c.79dup XP_016884818.1:p.Ala27GlyfsTer5
XM_017029330.2:c.79dup XP_016884819.1:p.Ala27GlyfsTer5
NM_000109.4:c.55dup NP_000100.3:p.Ala19GlyfsTer5
NM_004006.3:c.79dup MANE Select NP_003997.2:p.Ala27GlyfsTer5