Canonical Allele Identifier: CA2695234112

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32365096_32365108del , CM000685.2:g.32365096_32365108del	GRCh38
NC_000023.10:g.32383213_32383225del , CM000685.1:g.32383213_32383225del	GRCh37
NC_000023.9:g.32293134_32293146del	NCBI36
NG_012232.1:g.979505_979517del , LRG_199:g.979505_979517del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357033.9:c.4940_4952del MANE Select	ENSP00000354923.3:p.Thr1647IlefsTer6
ENST00000619831.5:c.908_920del	ENSP00000479270.2:p.Thr303IlefsTer6
ENST00000357033.8:c.4940_4952del	ENSP00000354923.3:p.Thr1647IlefsTer6
ENST00000378677.6:c.4928_4940del	ENSP00000367948.2:p.Thr1643IlefsTer6
ENST00000420596.5:c.188_200del	ENSP00000399897.1:p.Thr63IlefsTer6
ENST00000448370.5:c.94-395_94-383del	ENSP00000388559.1:n.94-395_94-383del
ENST00000488902.5:n.336-148042_336-148030del
ENST00000619831.4:c.4928_4940del	ENSP00000479270.1:p.Thr1643IlefsTer6
ENST00000620040.4:c.4940_4952del	ENSP00000478150.1:p.Thr1647IlefsTer6
NM_000109.3:c.4916_4928del	NP_000100.2:p.Thr1639IlefsTer6
NM_004006.2:c.4940_4952del , LRG_199t1:c.4940_4952del	NP_003997.1:p.Thr1647IlefsTer6
NM_004009.3:c.4928_4940del	NP_004000.1:p.Thr1643IlefsTer6
NM_004010.3:c.4571_4583del	NP_004001.1:p.Thr1524IlefsTer6
NM_004011.3:c.917_929del	NP_004002.2:p.Thr306IlefsTer6
NM_004012.3:c.908_920del	NP_004003.1:p.Thr303IlefsTer6
XM_006724468.2:c.4940_4952del	XP_006724531.1:p.Thr1647IlefsTer6
XM_006724469.2:c.4916_4928del	XP_006724532.1:p.Thr1639IlefsTer6
XM_006724470.2:c.4940_4952del	XP_006724533.1:p.Thr1647IlefsTer6
XM_006724471.2:c.4940_4952del	XP_006724534.1:p.Thr1647IlefsTer6
XM_006724472.2:c.4811_4823del	XP_006724535.1:p.Thr1604IlefsTer6
XM_006724473.2:c.4940_4952del	XP_006724536.1:p.Thr1647IlefsTer6
XM_006724474.2:c.4940_4952del	XP_006724537.1:p.Thr1647IlefsTer6
XM_006724475.2:c.4940_4952del	XP_006724538.1:p.Thr1647IlefsTer6
XM_011545467.1:c.4940_4952del	XP_011543769.1:p.Thr1647IlefsTer6
XM_011545468.1:c.4940_4952del	XP_011543770.1:p.Thr1647IlefsTer6
XM_011545469.1:c.4940_4952del	XP_011543771.1:p.Thr1647IlefsTer6
XM_006724469.3:c.4916_4928del	XP_006724532.1:p.Thr1639IlefsTer6
XM_006724470.3:c.4940_4952del	XP_006724533.1:p.Thr1647IlefsTer6
XM_006724474.3:c.4940_4952del	XP_006724537.1:p.Thr1647IlefsTer6
XM_011545468.2:c.4940_4952del	XP_011543770.1:p.Thr1647IlefsTer6
XM_017029328.1:c.4940_4952del	XP_016884817.1:p.Thr1647IlefsTer6
XM_017029329.1:c.4940_4952del	XP_016884818.1:p.Thr1647IlefsTer6
XM_017029330.2:c.4940_4952del	XP_016884819.1:p.Thr1647IlefsTer6
NM_000109.4:c.4916_4928del	NP_000100.3:p.Thr1639IlefsTer6
NM_004006.3:c.4940_4952del MANE Select	NP_003997.2:p.Thr1647IlefsTer6
NM_004011.4:c.917_929del	NP_004002.3:p.Thr306IlefsTer6
NM_004012.4:c.908_920del	NP_004003.2:p.Thr303IlefsTer6