Canonical Allele Identifier: CA412652981

Gene: DMD

Linked Data

• ClinVar Variation Id: 501095
• ClinVar RCV Id: RCV000595968 ; RCV000990566
• dbSNP Id: rs398123828
• MyVariant Identifiers: chrX:g.31198486C>A (hg19) ; chrX:g.31180369C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31180369C>A , CM000685.2:g.31180369C>A	GRCh38
NC_000023.10:g.31198486C>A , CM000685.1:g.31198486C>A	GRCh37
NC_000023.9:g.31108407C>A	NCBI36
NG_012232.1:g.2164241G>T , LRG_199:g.2164241G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.4932+1G>T	ENSP00000350765.3:n.4932+1G>T
ENST00000475732.3:n.2433+1G>T
ENST00000680162.2:c.882+1G>T	ENSP00000506634.2:n.882+1G>T
ENST00000680768.2:c.882+1G>T	ENSP00000506359.2:n.882+1G>T
ENST00000681989.1:n.884+1G>T
ENST00000682238.1:c.2706+1G>T	ENSP00000508124.1:n.2706+1G>T
ENST00000682322.1:c.882+1G>T	ENSP00000507690.1:n.882+1G>T
ENST00000682600.1:c.882+1G>T	ENSP00000507640.1:n.882+1G>T
ENST00000682769.1:n.717+1G>T
ENST00000683509.1:n.1603+1G>T
ENST00000683675.1:n.1185+1G>T
ENST00000683709.1:n.1604+1G>T
ENST00000683957.1:n.3578+1G>T
ENST00000684130.1:c.2706+1G>T	ENSP00000508037.1:n.2706+1G>T
ENST00000343523.7:c.1941+1G>T	ENSP00000340057.4:n.1941+1G>T
ENST00000357033.9:c.10086+1G>T MANE Select	ENSP00000354923.3:n.10086+1G>T
ENST00000475732.2:n.452+1G>T
ENST00000619831.5:c.6054+1G>T	ENSP00000479270.2:n.6054+1G>T
ENST00000620040.5:c.2706+1G>T	ENSP00000478150.2:n.2706+1G>T
ENST00000679641.1:c.*88+1G>T	ENSP00000506135.1:n.*88+1G>T
ENST00000679706.1:c.43+1G>T
ENST00000680162.1:c.759+1G>T	ENSP00000506634.1:n.759+1G>T
ENST00000680355.1:c.882+1G>T	ENSP00000506257.1:n.882+1G>T
ENST00000680557.1:c.603+23592G>T	ENSP00000505164.1:n.603+23592G>T
ENST00000680768.1:c.825+1G>T	ENSP00000506359.1:n.825+1G>T
ENST00000680961.1:c.*88+1G>T	ENSP00000506386.1:n.*88+1G>T
ENST00000681153.1:c.882+1G>T	ENSP00000505124.1:n.882+1G>T
ENST00000681654.1:n.1016+1G>T
ENST00000343523.6:c.1899+1G>T	ENSP00000340057.3:n.1899+1G>T
ENST00000357033.8:c.10086+1G>T	ENSP00000354923.3:n.10086+1G>T
ENST00000358062.6:c.3174+1G>T	ENSP00000350765.2:n.3174+1G>T
ENST00000359836.5:c.2706+1G>T	ENSP00000352894.1:n.2706+1G>T
ENST00000361471.8:c.882+1G>T	ENSP00000354464.4:n.882+1G>T
ENST00000378677.6:c.10074+1G>T	ENSP00000367948.2:n.10074+1G>T
ENST00000378680.6:c.882+1G>T	ENSP00000367951.2:n.882+1G>T
ENST00000378702.8:c.882+1G>T	ENSP00000367974.4:n.882+1G>T
ENST00000378705.3:c.456+1G>T	ENSP00000367977.3:n.456+1G>T
ENST00000378707.7:c.2706+1G>T	ENSP00000367979.3:n.2706+1G>T
ENST00000378723.7:c.882+1G>T	ENSP00000367997.3:n.882+1G>T
ENST00000474231.5:c.2706+1G>T	ENSP00000417123.1:n.2706+1G>T
ENST00000475732.1:n.302+1G>T
ENST00000541735.5:c.2706+1G>T	ENSP00000444119.1:n.2706+1G>T
ENST00000619831.4:c.10071+1G>T	ENSP00000479270.1:n.10071+1G>T
ENST00000620040.4:c.10083+1G>T	ENSP00000478150.1:n.10083+1G>T
NM_000109.3:c.10062+1G>T	NP_000100.2:n.10062+1G>T
NM_004006.2:c.10086+1G>T , LRG_199t1:c.10086+1G>T	NP_003997.1:n.10086+1G>T
NM_004009.3:c.10074+1G>T	NP_004000.1:n.10074+1G>T
NM_004010.3:c.9717+1G>T	NP_004001.1:n.9717+1G>T
NM_004011.3:c.6063+1G>T	NP_004002.2:n.6063+1G>T
NM_004012.3:c.6054+1G>T	NP_004003.1:n.6054+1G>T
NM_004013.2:c.2706+1G>T	NP_004004.1:n.2706+1G>T
NM_004014.2:c.1899+1G>T	NP_004005.1:n.1899+1G>T
NM_004015.2:c.882+1G>T	NP_004006.1:n.882+1G>T
NM_004016.2:c.882+1G>T	NP_004007.1:n.882+1G>T
NM_004017.2:c.882+1G>T	NP_004008.1:n.882+1G>T
NM_004018.2:c.882+1G>T	NP_004009.1:n.882+1G>T
NM_004019.2:c.882+1G>T	NP_004010.1:n.882+1G>T
NM_004020.3:c.2706+1G>T	NP_004011.2:n.2706+1G>T
NM_004021.2:c.2706+1G>T	NP_004012.1:n.2706+1G>T
NM_004022.2:c.2706+1G>T	NP_004013.1:n.2706+1G>T
NM_004023.2:c.2706+1G>T	NP_004014.1:n.2706+1G>T
XM_006724468.2:c.10086+1G>T	XP_006724531.1:n.10086+1G>T
XM_006724469.2:c.10062+1G>T	XP_006724532.1:n.10062+1G>T
XM_006724470.2:c.10086+1G>T	XP_006724533.1:n.10086+1G>T
XM_006724471.2:c.10086+1G>T	XP_006724534.1:n.10086+1G>T
XM_006724472.2:c.9957+1G>T	XP_006724535.1:n.9957+1G>T
XM_006724473.2:c.9948+1G>T	XP_006724536.1:n.9948+1G>T
XM_006724474.2:c.10086+1G>T	XP_006724537.1:n.10086+1G>T
XM_006724475.2:c.10086+1G>T	XP_006724538.1:n.10086+1G>T
XM_011545467.1:c.9963+1G>T	XP_011543769.1:n.9963+1G>T
XM_006724469.3:c.10062+1G>T	XP_006724532.1:n.10062+1G>T
XM_006724470.3:c.10086+1G>T	XP_006724533.1:n.10086+1G>T
XM_006724474.3:c.10086+1G>T	XP_006724537.1:n.10086+1G>T
XM_017029328.1:c.10086+1G>T	XP_016884817.1:n.10086+1G>T
XM_017029331.1:c.4260+1G>T	XP_016884820.1:n.4260+1G>T
NM_000109.4:c.10062+1G>T	NP_000100.3:n.10062+1G>T
NM_004006.3:c.10086+1G>T MANE Select	NP_003997.2:n.10086+1G>T
NM_004011.4:c.6063+1G>T	NP_004002.3:n.6063+1G>T
NM_004012.4:c.6054+1G>T	NP_004003.2:n.6054+1G>T
NM_004015.3:c.882+1G>T	NP_004006.1:n.882+1G>T
NM_004016.3:c.882+1G>T	NP_004007.1:n.882+1G>T
NM_004017.3:c.882+1G>T	NP_004008.1:n.882+1G>T
NM_004018.3:c.882+1G>T	NP_004009.1:n.882+1G>T
NM_004019.3:c.882+1G>T	NP_004010.1:n.882+1G>T
NM_004021.3:c.2706+1G>T	NP_004012.2:n.2706+1G>T
NM_004023.3:c.2706+1G>T	NP_004014.2:n.2706+1G>T
NM_004013.3:c.2706+1G>T	NP_004004.2:n.2706+1G>T
NM_004014.3:c.1899+1G>T	NP_004005.2:n.1899+1G>T
NM_004020.4:c.2706+1G>T	NP_004011.3:n.2706+1G>T
NM_004022.3:c.2706+1G>T	NP_004013.2:n.2706+1G>T