Canonical Allele Identifier: CA412649348

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.31224700T>A (hg19) ; chrX:g.31206583T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31206583T>A , CM000685.2:g.31206583T>A	GRCh38
NC_000023.10:g.31224700T>A , CM000685.1:g.31224700T>A	GRCh37
NC_000023.9:g.31134621T>A	NCBI36
NG_012232.1:g.2138027A>T , LRG_199:g.2138027A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000358062.7:c.4494A>T	ENSP00000350765.3:p.Arg1498Ser
ENST00000680162.2:c.444A>T	ENSP00000506634.2:p.Arg148Ser
ENST00000680768.2:c.444A>T	ENSP00000506359.2:p.Arg148Ser
ENST00000681989.1:n.446A>T
ENST00000682238.1:c.2268A>T	ENSP00000508124.1:p.Arg756Ser
ENST00000682322.1:c.444A>T	ENSP00000507690.1:p.Arg148Ser
ENST00000682600.1:c.444A>T	ENSP00000507640.1:p.Arg148Ser
ENST00000682769.1:n.446A>T
ENST00000683509.1:n.1165A>T
ENST00000683675.1:n.747A>T
ENST00000683709.1:n.1166A>T
ENST00000683957.1:n.3140A>T
ENST00000684130.1:c.2268A>T	ENSP00000508037.1:p.Arg756Ser
ENST00000343523.7:c.1503A>T	ENSP00000340057.4:p.Arg501Ser
ENST00000357033.9:c.9648A>T MANE Select	ENSP00000354923.3:p.Arg3216Ser
ENST00000619831.5:c.5616A>T	ENSP00000479270.2:p.Arg1872Ser
ENST00000620040.5:c.2268A>T	ENSP00000478150.2:p.Arg756Ser
ENST00000679641.1:c.444A>T	ENSP00000506135.1:p.Arg148Ser
ENST00000680162.1:c.321A>T	ENSP00000506634.1:p.Arg107Ser
ENST00000680355.1:c.444A>T	ENSP00000506257.1:p.Arg148Ser
ENST00000680557.1:c.444A>T	ENSP00000505164.1:p.Arg148Ser
ENST00000680768.1:c.387A>T	ENSP00000506359.1:p.Arg129Ser
ENST00000680961.1:c.2268A>T	ENSP00000506386.1:p.Arg756Ser
ENST00000681153.1:c.444A>T	ENSP00000505124.1:p.Arg148Ser
ENST00000681334.1:c.444A>T	ENSP00000506066.1:p.Arg148Ser
ENST00000681654.1:n.578A>T
ENST00000343523.6:c.1461A>T	ENSP00000340057.3:p.Arg487Ser
ENST00000357033.8:c.9648A>T	ENSP00000354923.3:p.Arg3216Ser
ENST00000358062.6:c.2736A>T	ENSP00000350765.2:p.Arg912Ser
ENST00000359836.5:c.2268A>T	ENSP00000352894.1:p.Arg756Ser
ENST00000361471.8:c.444A>T	ENSP00000354464.4:p.Arg148Ser
ENST00000378677.6:c.9636A>T	ENSP00000367948.2:p.Arg3212Ser
ENST00000378680.6:c.444A>T	ENSP00000367951.2:p.Arg148Ser
ENST00000378702.8:c.444A>T	ENSP00000367974.4:p.Arg148Ser
ENST00000378705.3:c.18A>T	ENSP00000367977.3:p.Arg6Ser
ENST00000378707.7:c.2268A>T	ENSP00000367979.3:p.Arg756Ser
ENST00000378723.7:c.444A>T	ENSP00000367997.3:p.Arg148Ser
ENST00000474231.5:c.2268A>T	ENSP00000417123.1:p.Arg756Ser
ENST00000541735.5:c.2268A>T	ENSP00000444119.1:p.Arg756Ser
ENST00000619831.4:c.9633A>T	ENSP00000479270.1:p.Arg3211Ser
ENST00000620040.4:c.9645A>T	ENSP00000478150.1:p.Arg3215Ser
NM_000109.3:c.9624A>T	NP_000100.2:p.Arg3208Ser
NM_004006.2:c.9648A>T , LRG_199t1:c.9648A>T	NP_003997.1:p.Arg3216Ser
NM_004009.3:c.9636A>T	NP_004000.1:p.Arg3212Ser
NM_004010.3:c.9279A>T	NP_004001.1:p.Arg3093Ser
NM_004011.3:c.5625A>T	NP_004002.2:p.Arg1875Ser
NM_004012.3:c.5616A>T	NP_004003.1:p.Arg1872Ser
NM_004013.2:c.2268A>T	NP_004004.1:p.Arg756Ser
NM_004014.2:c.1461A>T	NP_004005.1:p.Arg487Ser
NM_004015.2:c.444A>T	NP_004006.1:p.Arg148Ser
NM_004016.2:c.444A>T	NP_004007.1:p.Arg148Ser
NM_004017.2:c.444A>T	NP_004008.1:p.Arg148Ser
NM_004018.2:c.444A>T	NP_004009.1:p.Arg148Ser
NM_004019.2:c.444A>T	NP_004010.1:p.Arg148Ser
NM_004020.3:c.2268A>T	NP_004011.2:p.Arg756Ser
NM_004021.2:c.2268A>T	NP_004012.1:p.Arg756Ser
NM_004022.2:c.2268A>T	NP_004013.1:p.Arg756Ser
NM_004023.2:c.2268A>T	NP_004014.1:p.Arg756Ser
XM_006724468.2:c.9648A>T	XP_006724531.1:p.Arg3216Ser
XM_006724469.2:c.9624A>T	XP_006724532.1:p.Arg3208Ser
XM_006724470.2:c.9648A>T	XP_006724533.1:p.Arg3216Ser
XM_006724471.2:c.9648A>T	XP_006724534.1:p.Arg3216Ser
XM_006724472.2:c.9519A>T	XP_006724535.1:p.Arg3173Ser
XM_006724473.2:c.9510A>T	XP_006724536.1:p.Arg3170Ser
XM_006724474.2:c.9648A>T	XP_006724537.1:p.Arg3216Ser
XM_006724475.2:c.9648A>T	XP_006724538.1:p.Arg3216Ser
XM_011545467.1:c.9525A>T	XP_011543769.1:p.Arg3175Ser
XM_011545468.1:c.9648A>T	XP_011543770.1:p.Arg3216Ser
XM_006724469.3:c.9624A>T	XP_006724532.1:p.Arg3208Ser
XM_006724470.3:c.9648A>T	XP_006724533.1:p.Arg3216Ser
XM_006724474.3:c.9648A>T	XP_006724537.1:p.Arg3216Ser
XM_011545468.2:c.9648A>T	XP_011543770.1:p.Arg3216Ser
XM_017029328.1:c.9648A>T	XP_016884817.1:p.Arg3216Ser
XM_017029331.1:c.3822A>T	XP_016884820.1:p.Arg1274Ser
NM_000109.4:c.9624A>T	NP_000100.3:p.Arg3208Ser
NM_004006.3:c.9648A>T MANE Select	NP_003997.2:p.Arg3216Ser
NM_004011.4:c.5625A>T	NP_004002.3:p.Arg1875Ser
NM_004012.4:c.5616A>T	NP_004003.2:p.Arg1872Ser
NM_004015.3:c.444A>T	NP_004006.1:p.Arg148Ser
NM_004016.3:c.444A>T	NP_004007.1:p.Arg148Ser
NM_004017.3:c.444A>T	NP_004008.1:p.Arg148Ser
NM_004018.3:c.444A>T	NP_004009.1:p.Arg148Ser
NM_004019.3:c.444A>T	NP_004010.1:p.Arg148Ser
NM_004021.3:c.2268A>T	NP_004012.2:p.Arg756Ser
NM_004023.3:c.2268A>T	NP_004014.2:p.Arg756Ser
NM_004013.3:c.2268A>T	NP_004004.2:p.Arg756Ser
NM_004014.3:c.1461A>T	NP_004005.2:p.Arg487Ser
NM_004020.4:c.2268A>T	NP_004011.3:p.Arg756Ser
NM_004022.3:c.2268A>T	NP_004013.2:p.Arg756Ser