Canonical Allele Identifier: CA2693406217
Gene: DMD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32287780_32287781insC , CM000685.2:g.32287780_32287781insC GRCh38
NC_000023.10:g.32305897_32305898insC , CM000685.1:g.32305897_32305898insC GRCh37
NC_000023.9:g.32215818_32215819insC NCBI36
NG_012232.1:g.1056829_1056830insG , LRG_199:g.1056829_1056830insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000358062.7:c.964-80_964-79insG ENSP00000350765.3:n.964-80_964-79insG
ENST00000357033.9:c.6118-80_6118-79insG MANE Select ENSP00000354923.3:n.6118-80_6118-79insG
ENST00000619831.5:c.2086-80_2086-79insG ENSP00000479270.2:n.2086-80_2086-79insG
ENST00000357033.8:c.6118-80_6118-79insG ENSP00000354923.3:n.6118-80_6118-79insG
ENST00000378677.6:c.6106-80_6106-79insG ENSP00000367948.2:n.6106-80_6106-79insG
ENST00000488902.5:n.336-70718_336-70717insG
ENST00000619831.4:c.6106-80_6106-79insG ENSP00000479270.1:n.6106-80_6106-79insG
ENST00000620040.4:c.6118-80_6118-79insG ENSP00000478150.1:n.6118-80_6118-79insG
NM_000109.3:c.6094-80_6094-79insG NP_000100.2:n.6094-80_6094-79insG
NM_004006.2:c.6118-80_6118-79insG , LRG_199t1:c.6118-80_6118-79insG NP_003997.1:n.6118-80_6118-79insG
NM_004009.3:c.6106-80_6106-79insG NP_004000.1:n.6106-80_6106-79insG
NM_004010.3:c.5749-80_5749-79insG NP_004001.1:n.5749-80_5749-79insG
NM_004011.3:c.2095-80_2095-79insG NP_004002.2:n.2095-80_2095-79insG
NM_004012.3:c.2086-80_2086-79insG NP_004003.1:n.2086-80_2086-79insG
XM_006724468.2:c.6118-80_6118-79insG XP_006724531.1:n.6118-80_6118-79insG
XM_006724469.2:c.6094-80_6094-79insG XP_006724532.1:n.6094-80_6094-79insG
XM_006724470.2:c.6118-80_6118-79insG XP_006724533.1:n.6118-80_6118-79insG
XM_006724471.2:c.6118-80_6118-79insG XP_006724534.1:n.6118-80_6118-79insG
XM_006724472.2:c.5989-80_5989-79insG XP_006724535.1:n.5989-80_5989-79insG
XM_006724473.2:c.5980-80_5980-79insG XP_006724536.1:n.5980-80_5980-79insG
XM_006724474.2:c.6118-80_6118-79insG XP_006724537.1:n.6118-80_6118-79insG
XM_006724475.2:c.6118-80_6118-79insG XP_006724538.1:n.6118-80_6118-79insG
XM_011545467.1:c.5995-80_5995-79insG XP_011543769.1:n.5995-80_5995-79insG
XM_011545468.1:c.6118-80_6118-79insG XP_011543770.1:n.6118-80_6118-79insG
XM_006724469.3:c.6094-80_6094-79insG XP_006724532.1:n.6094-80_6094-79insG
XM_006724470.3:c.6118-80_6118-79insG XP_006724533.1:n.6118-80_6118-79insG
XM_006724474.3:c.6118-80_6118-79insG XP_006724537.1:n.6118-80_6118-79insG
XM_011545468.2:c.6118-80_6118-79insG XP_011543770.1:n.6118-80_6118-79insG
XM_017029328.1:c.6118-80_6118-79insG XP_016884817.1:n.6118-80_6118-79insG
XM_017029329.1:c.6118-80_6118-79insG XP_016884818.1:n.6118-80_6118-79insG
XM_017029330.2:c.6118-80_6118-79insG XP_016884819.1:n.6118-80_6118-79insG
XM_017029331.1:c.292-80_292-79insG XP_016884820.1:n.292-80_292-79insG
NM_000109.4:c.6094-80_6094-79insG NP_000100.3:n.6094-80_6094-79insG
NM_004006.3:c.6118-80_6118-79insG MANE Select NP_003997.2:n.6118-80_6118-79insG
NM_004011.4:c.2095-80_2095-79insG NP_004002.3:n.2095-80_2095-79insG
NM_004012.4:c.2086-80_2086-79insG NP_004003.2:n.2086-80_2086-79insG