Canonical Allele Identifier: CA2422815849
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32464717A= , CM000685.2:g.32464717A= GRCh38
NC_000023.10:g.32482834A= , CM000685.1:g.32482834A= GRCh37
NC_000023.9:g.32392755A= NCBI36
NG_012232.1:g.879893T= , LRG_199:g.879893T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682899.1:n.3370-18T=
ENST00000357033.9:c.3163-18T= MANE Select ENSP00000354923.3:n.3163-18T=
ENST00000357033.8:c.3163-18T= ENSP00000354923.3:n.3163-18T=
ENST00000378677.6:c.3151-18T= ENSP00000367948.2:n.3151-18T=
ENST00000420596.5:c.94-99518T= ENSP00000399897.1:n.94-99518T=
ENST00000448370.5:c.94-100007T= ENSP00000388559.1:n.94-100007T=
ENST00000488902.5:n.336-247654T=
ENST00000619831.4:c.3151-18T= ENSP00000479270.1:n.3151-18T=
ENST00000620040.4:c.3163-18T= ENSP00000478150.1:n.3163-18T=
NM_000109.3:c.3139-18T= NP_000100.2:n.3139-18T=
NM_004006.2:c.3163-18T= , LRG_199t1:c.3163-18T= NP_003997.1:n.3163-18T=
NM_004009.3:c.3151-18T= NP_004000.1:n.3151-18T=
NM_004010.3:c.2794-18T= NP_004001.1:n.2794-18T=
XM_006724468.2:c.3163-18T= XP_006724531.1:n.3163-18T=
XM_006724469.2:c.3139-18T= XP_006724532.1:n.3139-18T=
XM_006724470.2:c.3163-18T= XP_006724533.1:n.3163-18T=
XM_006724471.2:c.3163-18T= XP_006724534.1:n.3163-18T=
XM_006724472.2:c.3034-18T= XP_006724535.1:n.3034-18T=
XM_006724473.2:c.3163-18T= XP_006724536.1:n.3163-18T=
XM_006724474.2:c.3163-18T= XP_006724537.1:n.3163-18T=
XM_006724475.2:c.3163-18T= XP_006724538.1:n.3163-18T=
XM_011545467.1:c.3163-18T= XP_011543769.1:n.3163-18T=
XM_011545468.1:c.3163-18T= XP_011543770.1:n.3163-18T=
XM_011545469.1:c.3163-18T= XP_011543771.1:n.3163-18T=
XM_006724469.3:c.3139-18T= XP_006724532.1:n.3139-18T=
XM_006724470.3:c.3163-18T= XP_006724533.1:n.3163-18T=
XM_006724474.3:c.3163-18T= XP_006724537.1:n.3163-18T=
XM_011545468.2:c.3163-18T= XP_011543770.1:n.3163-18T=
XM_017029328.1:c.3163-18T= XP_016884817.1:n.3163-18T=
XM_017029329.1:c.3163-18T= XP_016884818.1:n.3163-18T=
XM_017029330.2:c.3163-18T= XP_016884819.1:n.3163-18T=
NM_000109.4:c.3139-18T= NP_000100.3:n.3139-18T=
NM_004006.3:c.3163-18T= MANE Select NP_003997.2:n.3163-18T=