Canonical Allele Identifier: CA2537527362
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32697896_32697897insT , CM000685.2:g.32697896_32697897insT GRCh38
NC_000023.10:g.32716013_32716014insT , CM000685.1:g.32716013_32716014insT GRCh37
NC_000023.9:g.32625934_32625935insT NCBI36
NG_012232.1:g.646713_646714insA , LRG_199:g.646713_646714insA

Transcript Alleles

HGVS Amino-acid change
ENST00000682071.1:c.564_565insA ENSP00000508133.1:p.Pro189ThrfsTer15
ENST00000682870.1:n.1118_1119insA
ENST00000682899.1:n.1140_1141insA
ENST00000682924.1:c.933_934insA ENSP00000508187.1:p.Pro312ThrfsTer15
ENST00000683985.1:n.1140_1141insA
ENST00000684165.1:n.1140_1141insA
ENST00000684237.1:c.831+1215_831+1216insA ENSP00000507277.1:n.831+1215_831+1216insA...
ENST00000684292.1:n.1140_1141insA
ENST00000288447.9:c.909_910insA ENSP00000288447.4:p.Pro304ThrfsTer15
ENST00000357033.9:c.933_934insA MANE Select ENSP00000354923.3:p.Pro312ThrfsTer15
ENST00000288447.8:c.909_910insA ENSP00000288447.4:p.Pro304ThrfsTer15
ENST00000357033.8:c.933_934insA ENSP00000354923.3:p.Pro312ThrfsTer15
ENST00000378677.6:c.921_922insA ENSP00000367948.2:p.Pro308ThrfsTer15
ENST00000420596.5:c.93+322242_93+322243insA ENSP00000399897.1:n.93+322242_93+322243in...
ENST00000447523.1:c.247-124051_247-124050insA ENSP00000395904.1:n.247-124051_247-124050...
ENST00000448370.5:c.93+322242_93+322243insA ENSP00000388559.1:n.93+322242_93+322243in...
ENST00000480751.1:n.86+118571_86+118572insA
ENST00000488902.5:n.335+322242_335+322243insA
ENST00000619831.4:c.921_922insA ENSP00000479270.1:p.Pro308ThrfsTer15
ENST00000620040.4:c.933_934insA ENSP00000478150.1:p.Pro312ThrfsTer15
NM_000109.3:c.909_910insA NP_000100.2:p.Pro304ThrfsTer15
NM_004006.2:c.933_934insA , LRG_199t1:c.933_934insA NP_003997.1:p.Pro312ThrfsTer15
NM_004009.3:c.921_922insA NP_004000.1:p.Pro308ThrfsTer15
NM_004010.3:c.564_565insA NP_004001.1:p.Pro189ThrfsTer15
XM_006724468.2:c.933_934insA XP_006724531.1:p.Pro312ThrfsTer15
XM_006724469.2:c.909_910insA XP_006724532.1:p.Pro304ThrfsTer15
XM_006724470.2:c.933_934insA XP_006724533.1:p.Pro312ThrfsTer15
XM_006724471.2:c.933_934insA XP_006724534.1:p.Pro312ThrfsTer15
XM_006724472.2:c.831+1215_831+1216insA XP_006724535.1:n.831+1215_831+1216insA
XM_006724473.2:c.933_934insA XP_006724536.1:p.Pro312ThrfsTer15
XM_006724474.2:c.933_934insA XP_006724537.1:p.Pro312ThrfsTer15
XM_006724475.2:c.933_934insA XP_006724538.1:p.Pro312ThrfsTer15
XM_011545467.1:c.933_934insA XP_011543769.1:p.Pro312ThrfsTer15
XM_011545468.1:c.933_934insA XP_011543770.1:p.Pro312ThrfsTer15
XM_011545469.1:c.933_934insA XP_011543771.1:p.Pro312ThrfsTer15
XM_006724469.3:c.909_910insA XP_006724532.1:p.Pro304ThrfsTer15
XM_006724470.3:c.933_934insA XP_006724533.1:p.Pro312ThrfsTer15
XM_006724474.3:c.933_934insA XP_006724537.1:p.Pro312ThrfsTer15
XM_011545468.2:c.933_934insA XP_011543770.1:p.Pro312ThrfsTer15
XM_017029328.1:c.933_934insA XP_016884817.1:p.Pro312ThrfsTer15
XM_017029329.1:c.933_934insA XP_016884818.1:p.Pro312ThrfsTer15
XM_017029330.2:c.933_934insA XP_016884819.1:p.Pro312ThrfsTer15
NM_000109.4:c.909_910insA NP_000100.3:p.Pro304ThrfsTer15
NM_004006.3:c.933_934insA MANE Select NP_003997.2:p.Pro312ThrfsTer15