Canonical Allele Identifier: CA2422815872
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32464760C= , CM000685.2:g.32464760C= GRCh38
NC_000023.10:g.32482877C= , CM000685.1:g.32482877C= GRCh37
NC_000023.9:g.32392798C= NCBI36
NG_012232.1:g.879850G= , LRG_199:g.879850G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682899.1:n.3370-61G=
ENST00000357033.9:c.3163-61G= MANE Select ENSP00000354923.3:n.3163-61G=
ENST00000357033.8:c.3163-61G= ENSP00000354923.3:n.3163-61G=
ENST00000378677.6:c.3151-61G= ENSP00000367948.2:n.3151-61G=
ENST00000420596.5:c.94-99561G= ENSP00000399897.1:n.94-99561G=
ENST00000448370.5:c.94-100050G= ENSP00000388559.1:n.94-100050G=
ENST00000488902.5:n.336-247697G=
ENST00000619831.4:c.3151-61G= ENSP00000479270.1:n.3151-61G=
ENST00000620040.4:c.3163-61G= ENSP00000478150.1:n.3163-61G=
NM_000109.3:c.3139-61G= NP_000100.2:n.3139-61G=
NM_004006.2:c.3163-61G= , LRG_199t1:c.3163-61G= NP_003997.1:n.3163-61G=
NM_004009.3:c.3151-61G= NP_004000.1:n.3151-61G=
NM_004010.3:c.2794-61G= NP_004001.1:n.2794-61G=
XM_006724468.2:c.3163-61G= XP_006724531.1:n.3163-61G=
XM_006724469.2:c.3139-61G= XP_006724532.1:n.3139-61G=
XM_006724470.2:c.3163-61G= XP_006724533.1:n.3163-61G=
XM_006724471.2:c.3163-61G= XP_006724534.1:n.3163-61G=
XM_006724472.2:c.3034-61G= XP_006724535.1:n.3034-61G=
XM_006724473.2:c.3163-61G= XP_006724536.1:n.3163-61G=
XM_006724474.2:c.3163-61G= XP_006724537.1:n.3163-61G=
XM_006724475.2:c.3163-61G= XP_006724538.1:n.3163-61G=
XM_011545467.1:c.3163-61G= XP_011543769.1:n.3163-61G=
XM_011545468.1:c.3163-61G= XP_011543770.1:n.3163-61G=
XM_011545469.1:c.3163-61G= XP_011543771.1:n.3163-61G=
XM_006724469.3:c.3139-61G= XP_006724532.1:n.3139-61G=
XM_006724470.3:c.3163-61G= XP_006724533.1:n.3163-61G=
XM_006724474.3:c.3163-61G= XP_006724537.1:n.3163-61G=
XM_011545468.2:c.3163-61G= XP_011543770.1:n.3163-61G=
XM_017029328.1:c.3163-61G= XP_016884817.1:n.3163-61G=
XM_017029329.1:c.3163-61G= XP_016884818.1:n.3163-61G=
XM_017029330.2:c.3163-61G= XP_016884819.1:n.3163-61G=
NM_000109.4:c.3139-61G= NP_000100.3:n.3139-61G=
NM_004006.3:c.3163-61G= MANE Select NP_003997.2:n.3163-61G=