Canonical Allele Identifier: CA275404
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 198502
dbSNP Id: rs796065333

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32809595dup , CM000685.2:g.32809595dup GRCh38
NC_000023.10:g.32827712dup , CM000685.1:g.32827712dup GRCh37
NC_000023.9:g.32737633dup NCBI36
NG_012232.1:g.535015dup , LRG_199:g.535015dup

Transcript Alleles

HGVS Amino-acid change
ENST00000682071.1:c.178dup ENSP00000508133.1:p.Trp60LeufsTer3
ENST00000682437.1:n.871dup
ENST00000682870.1:n.732dup
ENST00000682899.1:n.754dup
ENST00000682924.1:c.547dup ENSP00000508187.1:p.Trp183LeufsTer3
ENST00000683309.1:n.731dup
ENST00000683658.1:n.892dup
ENST00000683985.1:n.754dup
ENST00000684056.1:n.731dup
ENST00000684165.1:n.754dup
ENST00000684237.1:c.547dup ENSP00000507277.1:p.Trp183LeufsTer3
ENST00000684292.1:n.754dup
ENST00000684660.1:n.732dup
ENST00000288447.9:c.523dup ENSP00000288447.4:p.Trp175LeufsTer3
ENST00000357033.9:c.547dup MANE Select ENSP00000354923.3:p.Trp183LeufsTer3
ENST00000288447.8:c.523dup ENSP00000288447.4:p.Trp175LeufsTer3
ENST00000357033.8:c.547dup ENSP00000354923.3:p.Trp183LeufsTer3
ENST00000378677.6:c.535dup ENSP00000367948.2:p.Trp179LeufsTer3
ENST00000420596.5:c.93+210544dup ENSP00000399897.1:n.93+210544dup
ENST00000447523.1:c.246+13700dup ENSP00000395904.1:n.246+13700dup
ENST00000448370.5:c.93+210544dup ENSP00000388559.1:n.93+210544dup
ENST00000480751.1:n.86+6873dup
ENST00000488902.5:n.335+210544dup
ENST00000619831.4:c.535dup ENSP00000479270.1:p.Trp179LeufsTer3
ENST00000620040.4:c.547dup ENSP00000478150.1:p.Trp183LeufsTer3
NM_000109.3:c.523dup NP_000100.2:p.Trp175LeufsTer3
NM_004006.2:c.547dup , LRG_199t1:c.547dup NP_003997.1:p.Trp183LeufsTer3
NM_004009.3:c.535dup NP_004000.1:p.Trp179LeufsTer3
NM_004010.3:c.178dup NP_004001.1:p.Trp60LeufsTer3
XM_006724468.2:c.547dup XP_006724531.1:p.Trp183LeufsTer3
XM_006724469.2:c.523dup XP_006724532.1:p.Trp175LeufsTer3
XM_006724470.2:c.547dup XP_006724533.1:p.Trp183LeufsTer3
XM_006724471.2:c.547dup XP_006724534.1:p.Trp183LeufsTer3
XM_006724472.2:c.547dup XP_006724535.1:p.Trp183LeufsTer3
XM_006724473.2:c.547dup XP_006724536.1:p.Trp183LeufsTer3
XM_006724474.2:c.547dup XP_006724537.1:p.Trp183LeufsTer3
XM_006724475.2:c.547dup XP_006724538.1:p.Trp183LeufsTer3
XM_011545467.1:c.547dup XP_011543769.1:p.Trp183LeufsTer3
XM_011545468.1:c.547dup XP_011543770.1:p.Trp183LeufsTer3
XM_011545469.1:c.547dup XP_011543771.1:p.Trp183LeufsTer3
XM_006724469.3:c.523dup XP_006724532.1:p.Trp175LeufsTer3
XM_006724470.3:c.547dup XP_006724533.1:p.Trp183LeufsTer3
XM_006724474.3:c.547dup XP_006724537.1:p.Trp183LeufsTer3
XM_011545468.2:c.547dup XP_011543770.1:p.Trp183LeufsTer3
XM_017029328.1:c.547dup XP_016884817.1:p.Trp183LeufsTer3
XM_017029329.1:c.547dup XP_016884818.1:p.Trp183LeufsTer3
XM_017029330.2:c.547dup XP_016884819.1:p.Trp183LeufsTer3
NM_000109.4:c.523dup NP_000100.3:p.Trp175LeufsTer3
NM_004006.3:c.547dup MANE Select NP_003997.2:p.Trp183LeufsTer3