Canonical Allele Identifier: CA412654327

Gene: DMD

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31478332A>C , CM000685.2:g.31478332A>C	GRCh38
NC_000023.10:g.31496449A>C , CM000685.1:g.31496449A>C	GRCh37
NC_000023.9:g.31406370A>C	NCBI36
NG_012232.1:g.1866278T>G , LRG_199:g.1866278T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.3557T>G	ENSP00000350765.3:p.Leu1186Arg
ENST00000682238.1:c.1331T>G	ENSP00000508124.1:p.Leu444Arg
ENST00000683450.1:n.2176T>G
ENST00000683957.1:n.2203T>G
ENST00000684130.1:c.1331T>G	ENSP00000508037.1:p.Leu444Arg
ENST00000343523.7:c.566T>G	ENSP00000340057.4:p.Leu189Arg
ENST00000357033.9:c.8711T>G MANE Select	ENSP00000354923.3:p.Leu2904Arg
ENST00000619831.5:c.4679T>G	ENSP00000479270.2:p.Leu1560Arg
ENST00000620040.5:c.1331T>G	ENSP00000478150.2:p.Leu444Arg
ENST00000680961.1:c.1331T>G	ENSP00000506386.1:p.Leu444Arg
ENST00000681646.1:n.2372T>G
ENST00000343523.6:c.524T>G	ENSP00000340057.3:p.Leu175Arg
ENST00000357033.8:c.8711T>G	ENSP00000354923.3:p.Leu2904Arg
ENST00000358062.6:c.1799T>G	ENSP00000350765.2:p.Leu600Arg
ENST00000359836.5:c.1331T>G	ENSP00000352894.1:p.Leu444Arg
ENST00000378677.6:c.8699T>G	ENSP00000367948.2:p.Leu2900Arg
ENST00000378707.7:c.1331T>G	ENSP00000367979.3:p.Leu444Arg
ENST00000445312.1:n.768T>G
ENST00000474231.5:c.1331T>G	ENSP00000417123.1:p.Leu444Arg
ENST00000541735.5:c.1331T>G	ENSP00000444119.1:p.Leu444Arg
ENST00000619831.4:c.8696T>G	ENSP00000479270.1:p.Leu2899Arg
ENST00000620040.4:c.8708T>G	ENSP00000478150.1:p.Leu2903Arg
NM_000109.3:c.8687T>G	NP_000100.2:p.Leu2896Arg
NM_004006.2:c.8711T>G , LRG_199t1:c.8711T>G	NP_003997.1:p.Leu2904Arg
NM_004009.3:c.8699T>G	NP_004000.1:p.Leu2900Arg
NM_004010.3:c.8342T>G	NP_004001.1:p.Leu2781Arg
NM_004011.3:c.4688T>G	NP_004002.2:p.Leu1563Arg
NM_004012.3:c.4679T>G	NP_004003.1:p.Leu1560Arg
NM_004013.2:c.1331T>G	NP_004004.1:p.Leu444Arg
NM_004014.2:c.524T>G	NP_004005.1:p.Leu175Arg
NM_004020.3:c.1331T>G	NP_004011.2:p.Leu444Arg
NM_004021.2:c.1331T>G	NP_004012.1:p.Leu444Arg
NM_004022.2:c.1331T>G	NP_004013.1:p.Leu444Arg
NM_004023.2:c.1331T>G	NP_004014.1:p.Leu444Arg
XM_006724468.2:c.8711T>G	XP_006724531.1:p.Leu2904Arg
XM_006724469.2:c.8687T>G	XP_006724532.1:p.Leu2896Arg
XM_006724470.2:c.8711T>G	XP_006724533.1:p.Leu2904Arg
XM_006724471.2:c.8711T>G	XP_006724534.1:p.Leu2904Arg
XM_006724472.2:c.8582T>G	XP_006724535.1:p.Leu2861Arg
XM_006724473.2:c.8573T>G	XP_006724536.1:p.Leu2858Arg
XM_006724474.2:c.8711T>G	XP_006724537.1:p.Leu2904Arg
XM_006724475.2:c.8711T>G	XP_006724538.1:p.Leu2904Arg
XM_011545467.1:c.8588T>G	XP_011543769.1:p.Leu2863Arg
XM_011545468.1:c.8711T>G	XP_011543770.1:p.Leu2904Arg
XM_006724469.3:c.8687T>G	XP_006724532.1:p.Leu2896Arg
XM_006724470.3:c.8711T>G	XP_006724533.1:p.Leu2904Arg
XM_006724474.3:c.8711T>G	XP_006724537.1:p.Leu2904Arg
XM_011545468.2:c.8711T>G	XP_011543770.1:p.Leu2904Arg
XM_017029328.1:c.8711T>G	XP_016884817.1:p.Leu2904Arg
XM_017029331.1:c.2885T>G	XP_016884820.1:p.Leu962Arg
NM_000109.4:c.8687T>G	NP_000100.3:p.Leu2896Arg
NM_004006.3:c.8711T>G MANE Select	NP_003997.2:p.Leu2904Arg
NM_004011.4:c.4688T>G	NP_004002.3:p.Leu1563Arg
NM_004012.4:c.4679T>G	NP_004003.2:p.Leu1560Arg
NM_004021.3:c.1331T>G	NP_004012.2:p.Leu444Arg
NM_004023.3:c.1331T>G	NP_004014.2:p.Leu444Arg
NM_004013.3:c.1331T>G	NP_004004.2:p.Leu444Arg
NM_004014.3:c.524T>G	NP_004005.2:p.Leu175Arg
NM_004020.4:c.1331T>G	NP_004011.3:p.Leu444Arg
NM_004022.3:c.1331T>G	NP_004013.2:p.Leu444Arg