Canonical Allele Identifier: CA2422932263
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32697901G= , CM000685.2:g.32697901G= GRCh38
NC_000023.10:g.32716018G= , CM000685.1:g.32716018G= GRCh37
NC_000023.9:g.32625939G= NCBI36
NG_012232.1:g.646709C= , LRG_199:g.646709C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682071.1:c.560C= ENSP00000508133.1:p.Ser187=
ENST00000682870.1:n.1114C=
ENST00000682899.1:n.1136C=
ENST00000682924.1:c.929C= ENSP00000508187.1:p.Ser310=
ENST00000683985.1:n.1136C=
ENST00000684165.1:n.1136C=
ENST00000684237.1:c.831+1211C= ENSP00000507277.1:n.831+1211C=
ENST00000684292.1:n.1136C=
ENST00000288447.9:c.905C= ENSP00000288447.4:p.Ser302=
ENST00000357033.9:c.929C= MANE Select ENSP00000354923.3:p.Ser310=
ENST00000288447.8:c.905C= ENSP00000288447.4:p.Ser302=
ENST00000357033.8:c.929C= ENSP00000354923.3:p.Ser310=
ENST00000378677.6:c.917C= ENSP00000367948.2:p.Ser306=
ENST00000420596.5:c.93+322238C= ENSP00000399897.1:n.93+322238C=
ENST00000447523.1:c.247-124055C= ENSP00000395904.1:n.247-124055C=
ENST00000448370.5:c.93+322238C= ENSP00000388559.1:n.93+322238C=
ENST00000480751.1:n.86+118567C=
ENST00000488902.5:n.335+322238C=
ENST00000619831.4:c.917C= ENSP00000479270.1:p.Ser306=
ENST00000620040.4:c.929C= ENSP00000478150.1:p.Ser310=
NM_000109.3:c.905C= NP_000100.2:p.Ser302=
NM_004006.2:c.929C= , LRG_199t1:c.929C= NP_003997.1:p.Ser310=
NM_004009.3:c.917C= NP_004000.1:p.Ser306=
NM_004010.3:c.560C= NP_004001.1:p.Ser187=
XM_006724468.2:c.929C= XP_006724531.1:p.Ser310=
XM_006724469.2:c.905C= XP_006724532.1:p.Ser302=
XM_006724470.2:c.929C= XP_006724533.1:p.Ser310=
XM_006724471.2:c.929C= XP_006724534.1:p.Ser310=
XM_006724472.2:c.831+1211C= XP_006724535.1:n.831+1211C=
XM_006724473.2:c.929C= XP_006724536.1:p.Ser310=
XM_006724474.2:c.929C= XP_006724537.1:p.Ser310=
XM_006724475.2:c.929C= XP_006724538.1:p.Ser310=
XM_011545467.1:c.929C= XP_011543769.1:p.Ser310=
XM_011545468.1:c.929C= XP_011543770.1:p.Ser310=
XM_011545469.1:c.929C= XP_011543771.1:p.Ser310=
XM_006724469.3:c.905C= XP_006724532.1:p.Ser302=
XM_006724470.3:c.929C= XP_006724533.1:p.Ser310=
XM_006724474.3:c.929C= XP_006724537.1:p.Ser310=
XM_011545468.2:c.929C= XP_011543770.1:p.Ser310=
XM_017029328.1:c.929C= XP_016884817.1:p.Ser310=
XM_017029329.1:c.929C= XP_016884818.1:p.Ser310=
XM_017029330.2:c.929C= XP_016884819.1:p.Ser310=
NM_000109.4:c.905C= NP_000100.3:p.Ser302=
NM_004006.3:c.929C= MANE Select NP_003997.2:p.Ser310=