Canonical Allele Identifier: CA2422736443
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32287640G= , CM000685.2:g.32287640G= GRCh38
NC_000023.10:g.32305757G= , CM000685.1:g.32305757G= GRCh37
NC_000023.9:g.32215678G= NCBI36
NG_012232.1:g.1056970C= , LRG_199:g.1056970C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358062.7:c.1025C= ENSP00000350765.3:p.Thr342=
ENST00000357033.9:c.6179C= MANE Select ENSP00000354923.3:p.Thr2060=
ENST00000619831.5:c.2147C= ENSP00000479270.2:p.Thr716=
ENST00000357033.8:c.6179C= ENSP00000354923.3:p.Thr2060=
ENST00000378677.6:c.6167C= ENSP00000367948.2:p.Thr2056=
ENST00000488902.5:n.336-70577C=
ENST00000619831.4:c.6167C= ENSP00000479270.1:p.Thr2056=
ENST00000620040.4:c.6179C= ENSP00000478150.1:p.Thr2060=
NM_000109.3:c.6155C= NP_000100.2:p.Thr2052=
NM_004006.2:c.6179C= , LRG_199t1:c.6179C= NP_003997.1:p.Thr2060=
NM_004009.3:c.6167C= NP_004000.1:p.Thr2056=
NM_004010.3:c.5810C= NP_004001.1:p.Thr1937=
NM_004011.3:c.2156C= NP_004002.2:p.Thr719=
NM_004012.3:c.2147C= NP_004003.1:p.Thr716=
XM_006724468.2:c.6179C= XP_006724531.1:p.Thr2060=
XM_006724469.2:c.6155C= XP_006724532.1:p.Thr2052=
XM_006724470.2:c.6179C= XP_006724533.1:p.Thr2060=
XM_006724471.2:c.6179C= XP_006724534.1:p.Thr2060=
XM_006724472.2:c.6050C= XP_006724535.1:p.Thr2017=
XM_006724473.2:c.6041C= XP_006724536.1:p.Thr2014=
XM_006724474.2:c.6179C= XP_006724537.1:p.Thr2060=
XM_006724475.2:c.6179C= XP_006724538.1:p.Thr2060=
XM_011545467.1:c.6056C= XP_011543769.1:p.Thr2019=
XM_011545468.1:c.6179C= XP_011543770.1:p.Thr2060=
XM_006724469.3:c.6155C= XP_006724532.1:p.Thr2052=
XM_006724470.3:c.6179C= XP_006724533.1:p.Thr2060=
XM_006724474.3:c.6179C= XP_006724537.1:p.Thr2060=
XM_011545468.2:c.6179C= XP_011543770.1:p.Thr2060=
XM_017029328.1:c.6179C= XP_016884817.1:p.Thr2060=
XM_017029329.1:c.6179C= XP_016884818.1:p.Thr2060=
XM_017029330.2:c.6179C= XP_016884819.1:p.Thr2060=
XM_017029331.1:c.353C= XP_016884820.1:p.Thr118=
NM_000109.4:c.6155C= NP_000100.3:p.Thr2052=
NM_004006.3:c.6179C= MANE Select NP_003997.2:p.Thr2060=
NM_004011.4:c.2156C= NP_004002.3:p.Thr719=
NM_004012.4:c.2147C= NP_004003.2:p.Thr716=