Canonical Allele Identifier: CA2422736253
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32287134_32287137delinsATTT , CM000685.2:g.32287134_32287137delinsATTT GRCh38
NC_000023.10:g.32305251_32305254delinsATTT , CM000685.1:g.32305251_32305254delinsATTT GRCh37
NC_000023.9:g.32215172_32215175delinsATTT NCBI36
NG_012232.1:g.1057473_1057476delinsAAAT , LRG_199:g.1057473_1057476delinsAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000358062.7:c.1136+392_1136+395delinsAAAT ENSP00000350765.3:n.1136+392_1136+395delinsAAAT
ENST00000357033.9:c.6290+392_6290+395delinsAAAT MANE Select ENSP00000354923.3:n.6290+392_6290+395delinsAAAT
ENST00000619831.5:c.2258+392_2258+395delinsAAAT ENSP00000479270.2:n.2258+392_2258+395delinsAAAT
ENST00000357033.8:c.6290+392_6290+395delinsAAAT ENSP00000354923.3:n.6290+392_6290+395delinsAAAT
ENST00000378677.6:c.6278+392_6278+395delinsAAAT ENSP00000367948.2:n.6278+392_6278+395delinsAAAT
ENST00000488902.5:n.336-70074_336-70071delinsAAAT
ENST00000619831.4:c.6278+392_6278+395delinsAAAT ENSP00000479270.1:n.6278+392_6278+395delinsAAAT
ENST00000620040.4:c.6290+392_6290+395delinsAAAT ENSP00000478150.1:n.6290+392_6290+395delinsAAAT
NM_000109.3:c.6266+392_6266+395delinsAAAT NP_000100.2:n.6266+392_6266+395delinsAAAT
NM_004006.2:c.6290+392_6290+395delinsAAAT , LRG_199t1:c.6290+392_6290+395delinsAAAT NP_003997.1:n.6290+392_6290+395delinsAAAT
NM_004009.3:c.6278+392_6278+395delinsAAAT NP_004000.1:n.6278+392_6278+395delinsAAAT
NM_004010.3:c.5921+392_5921+395delinsAAAT NP_004001.1:n.5921+392_5921+395delinsAAAT
NM_004011.3:c.2267+392_2267+395delinsAAAT NP_004002.2:n.2267+392_2267+395delinsAAAT
NM_004012.3:c.2258+392_2258+395delinsAAAT NP_004003.1:n.2258+392_2258+395delinsAAAT
XM_006724468.2:c.6290+392_6290+395delinsAAAT XP_006724531.1:n.6290+392_6290+395delinsAAAT
XM_006724469.2:c.6266+392_6266+395delinsAAAT XP_006724532.1:n.6266+392_6266+395delinsAAAT
XM_006724470.2:c.6290+392_6290+395delinsAAAT XP_006724533.1:n.6290+392_6290+395delinsAAAT
XM_006724471.2:c.6290+392_6290+395delinsAAAT XP_006724534.1:n.6290+392_6290+395delinsAAAT
XM_006724472.2:c.6161+392_6161+395delinsAAAT XP_006724535.1:n.6161+392_6161+395delinsAAAT
XM_006724473.2:c.6152+392_6152+395delinsAAAT XP_006724536.1:n.6152+392_6152+395delinsAAAT
XM_006724474.2:c.6290+392_6290+395delinsAAAT XP_006724537.1:n.6290+392_6290+395delinsAAAT
XM_006724475.2:c.6290+392_6290+395delinsAAAT XP_006724538.1:n.6290+392_6290+395delinsAAAT
XM_011545467.1:c.6167+392_6167+395delinsAAAT XP_011543769.1:n.6167+392_6167+395delinsAAAT
XM_011545468.1:c.6290+392_6290+395delinsAAAT XP_011543770.1:n.6290+392_6290+395delinsAAAT
XM_006724469.3:c.6266+392_6266+395delinsAAAT XP_006724532.1:n.6266+392_6266+395delinsAAAT
XM_006724470.3:c.6290+392_6290+395delinsAAAT XP_006724533.1:n.6290+392_6290+395delinsAAAT
XM_006724474.3:c.6290+392_6290+395delinsAAAT XP_006724537.1:n.6290+392_6290+395delinsAAAT
XM_011545468.2:c.6290+392_6290+395delinsAAAT XP_011543770.1:n.6290+392_6290+395delinsAAAT
XM_017029328.1:c.6290+392_6290+395delinsAAAT XP_016884817.1:n.6290+392_6290+395delinsAAAT
XM_017029329.1:c.6290+392_6290+395delinsAAAT XP_016884818.1:n.6290+392_6290+395delinsAAAT
XM_017029330.2:c.6290+392_6290+395delinsAAAT XP_016884819.1:n.6290+392_6290+395delinsAAAT
XM_017029331.1:c.464+392_464+395delinsAAAT XP_016884820.1:n.464+392_464+395delinsAAAT
NM_000109.4:c.6266+392_6266+395delinsAAAT NP_000100.3:n.6266+392_6266+395delinsAAAT
NM_004006.3:c.6290+392_6290+395delinsAAAT MANE Select NP_003997.2:n.6290+392_6290+395delinsAAAT
NM_004011.4:c.2267+392_2267+395delinsAAAT NP_004002.3:n.2267+392_2267+395delinsAAAT
NM_004012.4:c.2258+392_2258+395delinsAAAT NP_004003.2:n.2258+392_2258+395delinsAAAT