Canonical Allele Identifier: CA412654332

Gene: DMD

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31478335A>T , CM000685.2:g.31478335A>T	GRCh38
NC_000023.10:g.31496452A>T , CM000685.1:g.31496452A>T	GRCh37
NC_000023.9:g.31406373A>T	NCBI36
NG_012232.1:g.1866275T>A , LRG_199:g.1866275T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.3554T>A	ENSP00000350765.3:p.Leu1185His
ENST00000682238.1:c.1328T>A	ENSP00000508124.1:p.Leu443His
ENST00000683450.1:n.2173T>A
ENST00000683957.1:n.2200T>A
ENST00000684130.1:c.1328T>A	ENSP00000508037.1:p.Leu443His
ENST00000343523.7:c.563T>A	ENSP00000340057.4:p.Leu188His
ENST00000357033.9:c.8708T>A MANE Select	ENSP00000354923.3:p.Leu2903His
ENST00000619831.5:c.4676T>A	ENSP00000479270.2:p.Leu1559His
ENST00000620040.5:c.1328T>A	ENSP00000478150.2:p.Leu443His
ENST00000680961.1:c.1328T>A	ENSP00000506386.1:p.Leu443His
ENST00000681646.1:n.2369T>A
ENST00000343523.6:c.521T>A	ENSP00000340057.3:p.Leu174His
ENST00000357033.8:c.8708T>A	ENSP00000354923.3:p.Leu2903His
ENST00000358062.6:c.1796T>A	ENSP00000350765.2:p.Leu599His
ENST00000359836.5:c.1328T>A	ENSP00000352894.1:p.Leu443His
ENST00000378677.6:c.8696T>A	ENSP00000367948.2:p.Leu2899His
ENST00000378707.7:c.1328T>A	ENSP00000367979.3:p.Leu443His
ENST00000445312.1:n.765T>A
ENST00000474231.5:c.1328T>A	ENSP00000417123.1:p.Leu443His
ENST00000541735.5:c.1328T>A	ENSP00000444119.1:p.Leu443His
ENST00000619831.4:c.8693T>A	ENSP00000479270.1:p.Leu2898His
ENST00000620040.4:c.8705T>A	ENSP00000478150.1:p.Leu2902His
NM_000109.3:c.8684T>A	NP_000100.2:p.Leu2895His
NM_004006.2:c.8708T>A , LRG_199t1:c.8708T>A	NP_003997.1:p.Leu2903His
NM_004009.3:c.8696T>A	NP_004000.1:p.Leu2899His
NM_004010.3:c.8339T>A	NP_004001.1:p.Leu2780His
NM_004011.3:c.4685T>A	NP_004002.2:p.Leu1562His
NM_004012.3:c.4676T>A	NP_004003.1:p.Leu1559His
NM_004013.2:c.1328T>A	NP_004004.1:p.Leu443His
NM_004014.2:c.521T>A	NP_004005.1:p.Leu174His
NM_004020.3:c.1328T>A	NP_004011.2:p.Leu443His
NM_004021.2:c.1328T>A	NP_004012.1:p.Leu443His
NM_004022.2:c.1328T>A	NP_004013.1:p.Leu443His
NM_004023.2:c.1328T>A	NP_004014.1:p.Leu443His
XM_006724468.2:c.8708T>A	XP_006724531.1:p.Leu2903His
XM_006724469.2:c.8684T>A	XP_006724532.1:p.Leu2895His
XM_006724470.2:c.8708T>A	XP_006724533.1:p.Leu2903His
XM_006724471.2:c.8708T>A	XP_006724534.1:p.Leu2903His
XM_006724472.2:c.8579T>A	XP_006724535.1:p.Leu2860His
XM_006724473.2:c.8570T>A	XP_006724536.1:p.Leu2857His
XM_006724474.2:c.8708T>A	XP_006724537.1:p.Leu2903His
XM_006724475.2:c.8708T>A	XP_006724538.1:p.Leu2903His
XM_011545467.1:c.8585T>A	XP_011543769.1:p.Leu2862His
XM_011545468.1:c.8708T>A	XP_011543770.1:p.Leu2903His
XM_006724469.3:c.8684T>A	XP_006724532.1:p.Leu2895His
XM_006724470.3:c.8708T>A	XP_006724533.1:p.Leu2903His
XM_006724474.3:c.8708T>A	XP_006724537.1:p.Leu2903His
XM_011545468.2:c.8708T>A	XP_011543770.1:p.Leu2903His
XM_017029328.1:c.8708T>A	XP_016884817.1:p.Leu2903His
XM_017029331.1:c.2882T>A	XP_016884820.1:p.Leu961His
NM_000109.4:c.8684T>A	NP_000100.3:p.Leu2895His
NM_004006.3:c.8708T>A MANE Select	NP_003997.2:p.Leu2903His
NM_004011.4:c.4685T>A	NP_004002.3:p.Leu1562His
NM_004012.4:c.4676T>A	NP_004003.2:p.Leu1559His
NM_004021.3:c.1328T>A	NP_004012.2:p.Leu443His
NM_004023.3:c.1328T>A	NP_004014.2:p.Leu443His
NM_004013.3:c.1328T>A	NP_004004.2:p.Leu443His
NM_004014.3:c.521T>A	NP_004005.2:p.Leu174His
NM_004020.4:c.1328T>A	NP_004011.3:p.Leu443His
NM_004022.3:c.1328T>A	NP_004013.2:p.Leu443His