Canonical Allele Identifier: CA412652791

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.31196842A>C (hg19) ; chrX:g.31178725A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31178725A>C , CM000685.2:g.31178725A>C	GRCh38
NC_000023.10:g.31196842A>C , CM000685.1:g.31196842A>C	GRCh37
NC_000023.9:g.31106763A>C	NCBI36
NG_012232.1:g.2165885T>G , LRG_199:g.2165885T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.5013T>G	ENSP00000350765.3:p.His1671Gln
ENST00000475732.3:n.2514T>G
ENST00000680162.2:c.963T>G	ENSP00000506634.2:p.His321Gln
ENST00000680768.2:c.963T>G	ENSP00000506359.2:p.His321Gln
ENST00000681989.1:n.965T>G
ENST00000682238.1:c.2787T>G	ENSP00000508124.1:p.His929Gln
ENST00000682322.1:c.963T>G	ENSP00000507690.1:p.His321Gln
ENST00000682600.1:c.963T>G	ENSP00000507640.1:p.His321Gln
ENST00000682769.1:n.798T>G
ENST00000683509.1:n.1684T>G
ENST00000683675.1:n.1266T>G
ENST00000683709.1:n.1685T>G
ENST00000683957.1:n.3659T>G
ENST00000684130.1:c.2787T>G	ENSP00000508037.1:p.His929Gln
ENST00000343523.7:c.2022T>G	ENSP00000340057.4:p.His674Gln
ENST00000357033.9:c.10167T>G MANE Select	ENSP00000354923.3:p.His3389Gln
ENST00000475732.2:n.533T>G
ENST00000619831.5:c.6135T>G	ENSP00000479270.2:p.His2045Gln
ENST00000620040.5:c.2787T>G	ENSP00000478150.2:p.His929Gln
ENST00000679641.1:c.*169T>G	ENSP00000506135.1:n.*169T>G
ENST00000679706.1:c.124T>G
ENST00000680162.1:c.840T>G	ENSP00000506634.1:p.His280Gln
ENST00000680355.1:c.963T>G	ENSP00000506257.1:p.His321Gln
ENST00000680557.1:c.603+25236T>G	ENSP00000505164.1:n.603+25236T>G
ENST00000680768.1:c.906T>G	ENSP00000506359.1:p.His302Gln
ENST00000680961.1:c.*169T>G	ENSP00000506386.1:n.*169T>G
ENST00000681153.1:c.963T>G	ENSP00000505124.1:p.His321Gln
ENST00000681654.1:n.1097T>G
ENST00000343523.6:c.1980T>G	ENSP00000340057.3:p.His660Gln
ENST00000357033.8:c.10167T>G	ENSP00000354923.3:p.His3389Gln
ENST00000358062.6:c.3255T>G	ENSP00000350765.2:p.His1085Gln
ENST00000359836.5:c.2787T>G	ENSP00000352894.1:p.His929Gln
ENST00000361471.8:c.963T>G	ENSP00000354464.4:p.His321Gln
ENST00000378677.6:c.10155T>G	ENSP00000367948.2:p.His3385Gln
ENST00000378680.6:c.963T>G	ENSP00000367951.2:p.His321Gln
ENST00000378702.8:c.963T>G	ENSP00000367974.4:p.His321Gln
ENST00000378705.3:c.537T>G	ENSP00000367977.3:p.His179Gln
ENST00000378707.7:c.2787T>G	ENSP00000367979.3:p.His929Gln
ENST00000378723.7:c.963T>G	ENSP00000367997.3:p.His321Gln
ENST00000474231.5:c.2787T>G	ENSP00000417123.1:p.His929Gln
ENST00000475732.1:n.383T>G
ENST00000541735.5:c.2787T>G	ENSP00000444119.1:p.His929Gln
ENST00000619831.4:c.10152T>G	ENSP00000479270.1:p.His3384Gln
ENST00000620040.4:c.10164T>G	ENSP00000478150.1:p.His3388Gln
NM_000109.3:c.10143T>G	NP_000100.2:p.His3381Gln
NM_004006.2:c.10167T>G , LRG_199t1:c.10167T>G	NP_003997.1:p.His3389Gln
NM_004009.3:c.10155T>G	NP_004000.1:p.His3385Gln
NM_004010.3:c.9798T>G	NP_004001.1:p.His3266Gln
NM_004011.3:c.6144T>G	NP_004002.2:p.His2048Gln
NM_004012.3:c.6135T>G	NP_004003.1:p.His2045Gln
NM_004013.2:c.2787T>G	NP_004004.1:p.His929Gln
NM_004014.2:c.1980T>G	NP_004005.1:p.His660Gln
NM_004015.2:c.963T>G	NP_004006.1:p.His321Gln
NM_004016.2:c.963T>G	NP_004007.1:p.His321Gln
NM_004017.2:c.963T>G	NP_004008.1:p.His321Gln
NM_004018.2:c.963T>G	NP_004009.1:p.His321Gln
NM_004019.2:c.963T>G	NP_004010.1:p.His321Gln
NM_004020.3:c.2787T>G	NP_004011.2:p.His929Gln
NM_004021.2:c.2787T>G	NP_004012.1:p.His929Gln
NM_004022.2:c.2787T>G	NP_004013.1:p.His929Gln
NM_004023.2:c.2787T>G	NP_004014.1:p.His929Gln
XM_006724468.2:c.10167T>G	XP_006724531.1:p.His3389Gln
XM_006724469.2:c.10143T>G	XP_006724532.1:p.His3381Gln
XM_006724470.2:c.10167T>G	XP_006724533.1:p.His3389Gln
XM_006724471.2:c.10167T>G	XP_006724534.1:p.His3389Gln
XM_006724472.2:c.10038T>G	XP_006724535.1:p.His3346Gln
XM_006724473.2:c.10029T>G	XP_006724536.1:p.His3343Gln
XM_006724474.2:c.10167T>G	XP_006724537.1:p.His3389Gln
XM_006724475.2:c.10167T>G	XP_006724538.1:p.His3389Gln
XM_011545467.1:c.10044T>G	XP_011543769.1:p.His3348Gln
XM_006724469.3:c.10143T>G	XP_006724532.1:p.His3381Gln
XM_006724470.3:c.10167T>G	XP_006724533.1:p.His3389Gln
XM_006724474.3:c.10167T>G	XP_006724537.1:p.His3389Gln
XM_017029328.1:c.10167T>G	XP_016884817.1:p.His3389Gln
XM_017029331.1:c.4341T>G	XP_016884820.1:p.His1447Gln
NM_000109.4:c.10143T>G	NP_000100.3:p.His3381Gln
NM_004006.3:c.10167T>G MANE Select	NP_003997.2:p.His3389Gln
NM_004011.4:c.6144T>G	NP_004002.3:p.His2048Gln
NM_004012.4:c.6135T>G	NP_004003.2:p.His2045Gln
NM_004015.3:c.963T>G	NP_004006.1:p.His321Gln
NM_004016.3:c.963T>G	NP_004007.1:p.His321Gln
NM_004017.3:c.963T>G	NP_004008.1:p.His321Gln
NM_004018.3:c.963T>G	NP_004009.1:p.His321Gln
NM_004019.3:c.963T>G	NP_004010.1:p.His321Gln
NM_004021.3:c.2787T>G	NP_004012.2:p.His929Gln
NM_004023.3:c.2787T>G	NP_004014.2:p.His929Gln
NM_004013.3:c.2787T>G	NP_004004.2:p.His929Gln
NM_004014.3:c.1980T>G	NP_004005.2:p.His660Gln
NM_004020.4:c.2787T>G	NP_004011.3:p.His929Gln
NM_004022.3:c.2787T>G	NP_004013.2:p.His929Gln