Canonical Allele Identifier: CA2422932266
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32697906G= , CM000685.2:g.32697906G= GRCh38
NC_000023.10:g.32716023G= , CM000685.1:g.32716023G= GRCh37
NC_000023.9:g.32625944G= NCBI36
NG_012232.1:g.646704C= , LRG_199:g.646704C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682071.1:c.555C= ENSP00000508133.1:p.Thr185=
ENST00000682870.1:n.1109C=
ENST00000682899.1:n.1131C=
ENST00000682924.1:c.924C= ENSP00000508187.1:p.Thr308=
ENST00000683985.1:n.1131C=
ENST00000684165.1:n.1131C=
ENST00000684237.1:c.831+1206C= ENSP00000507277.1:n.831+1206C=
ENST00000684292.1:n.1131C=
ENST00000288447.9:c.900C= ENSP00000288447.4:p.Thr300=
ENST00000357033.9:c.924C= MANE Select ENSP00000354923.3:p.Thr308=
ENST00000288447.8:c.900C= ENSP00000288447.4:p.Thr300=
ENST00000357033.8:c.924C= ENSP00000354923.3:p.Thr308=
ENST00000378677.6:c.912C= ENSP00000367948.2:p.Thr304=
ENST00000420596.5:c.93+322233C= ENSP00000399897.1:n.93+322233C=
ENST00000447523.1:c.247-124060C= ENSP00000395904.1:n.247-124060C=
ENST00000448370.5:c.93+322233C= ENSP00000388559.1:n.93+322233C=
ENST00000480751.1:n.86+118562C=
ENST00000488902.5:n.335+322233C=
ENST00000619831.4:c.912C= ENSP00000479270.1:p.Thr304=
ENST00000620040.4:c.924C= ENSP00000478150.1:p.Thr308=
NM_000109.3:c.900C= NP_000100.2:p.Thr300=
NM_004006.2:c.924C= , LRG_199t1:c.924C= NP_003997.1:p.Thr308=
NM_004009.3:c.912C= NP_004000.1:p.Thr304=
NM_004010.3:c.555C= NP_004001.1:p.Thr185=
XM_006724468.2:c.924C= XP_006724531.1:p.Thr308=
XM_006724469.2:c.900C= XP_006724532.1:p.Thr300=
XM_006724470.2:c.924C= XP_006724533.1:p.Thr308=
XM_006724471.2:c.924C= XP_006724534.1:p.Thr308=
XM_006724472.2:c.831+1206C= XP_006724535.1:n.831+1206C=
XM_006724473.2:c.924C= XP_006724536.1:p.Thr308=
XM_006724474.2:c.924C= XP_006724537.1:p.Thr308=
XM_006724475.2:c.924C= XP_006724538.1:p.Thr308=
XM_011545467.1:c.924C= XP_011543769.1:p.Thr308=
XM_011545468.1:c.924C= XP_011543770.1:p.Thr308=
XM_011545469.1:c.924C= XP_011543771.1:p.Thr308=
XM_006724469.3:c.900C= XP_006724532.1:p.Thr300=
XM_006724470.3:c.924C= XP_006724533.1:p.Thr308=
XM_006724474.3:c.924C= XP_006724537.1:p.Thr308=
XM_011545468.2:c.924C= XP_011543770.1:p.Thr308=
XM_017029328.1:c.924C= XP_016884817.1:p.Thr308=
XM_017029329.1:c.924C= XP_016884818.1:p.Thr308=
XM_017029330.2:c.924C= XP_016884819.1:p.Thr308=
NM_000109.4:c.900C= NP_000100.3:p.Thr300=
NM_004006.3:c.924C= MANE Select NP_003997.2:p.Thr308=