Canonical Allele Identifier: CA412655158

Gene: DMD

Linked Data

• gnomAD v4: X-31444542-T-C
• MyVariant Identifiers: chrX:g.31462659T>C (hg19) ; chrX:g.31444542T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31444542T>C , CM000685.2:g.31444542T>C	GRCh38
NC_000023.10:g.31462659T>C , CM000685.1:g.31462659T>C	GRCh37
NC_000023.9:g.31372580T>C	NCBI36
NG_012232.1:g.1900068A>G , LRG_199:g.1900068A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.3869A>G	ENSP00000350765.3:p.Gln1290Arg
ENST00000682238.1:c.1643A>G	ENSP00000508124.1:p.Gln548Arg
ENST00000683450.1:n.2488A>G
ENST00000683957.1:n.2515A>G
ENST00000684130.1:c.1643A>G	ENSP00000508037.1:p.Gln548Arg
ENST00000343523.7:c.878A>G	ENSP00000340057.4:p.Gln293Arg
ENST00000357033.9:c.9023A>G MANE Select	ENSP00000354923.3:p.Gln3008Arg
ENST00000619831.5:c.4991A>G	ENSP00000479270.2:p.Gln1664Arg
ENST00000620040.5:c.1643A>G	ENSP00000478150.2:p.Gln548Arg
ENST00000680961.1:c.1643A>G	ENSP00000506386.1:p.Gln548Arg
ENST00000681646.1:n.2684A>G
ENST00000343523.6:c.836A>G	ENSP00000340057.3:p.Gln279Arg
ENST00000357033.8:c.9023A>G	ENSP00000354923.3:p.Gln3008Arg
ENST00000358062.6:c.2111A>G	ENSP00000350765.2:p.Gln704Arg
ENST00000359836.5:c.1643A>G	ENSP00000352894.1:p.Gln548Arg
ENST00000378677.6:c.9011A>G	ENSP00000367948.2:p.Gln3004Arg
ENST00000378707.7:c.1643A>G	ENSP00000367979.3:p.Gln548Arg
ENST00000474231.5:c.1643A>G	ENSP00000417123.1:p.Gln548Arg
ENST00000541735.5:c.1643A>G	ENSP00000444119.1:p.Gln548Arg
ENST00000619831.4:c.9008A>G	ENSP00000479270.1:p.Gln3003Arg
ENST00000620040.4:c.9020A>G	ENSP00000478150.1:p.Gln3007Arg
NM_000109.3:c.8999A>G	NP_000100.2:p.Gln3000Arg
NM_004006.2:c.9023A>G , LRG_199t1:c.9023A>G	NP_003997.1:p.Gln3008Arg
NM_004009.3:c.9011A>G	NP_004000.1:p.Gln3004Arg
NM_004010.3:c.8654A>G	NP_004001.1:p.Gln2885Arg
NM_004011.3:c.5000A>G	NP_004002.2:p.Gln1667Arg
NM_004012.3:c.4991A>G	NP_004003.1:p.Gln1664Arg
NM_004013.2:c.1643A>G	NP_004004.1:p.Gln548Arg
NM_004014.2:c.836A>G	NP_004005.1:p.Gln279Arg
NM_004020.3:c.1643A>G	NP_004011.2:p.Gln548Arg
NM_004021.2:c.1643A>G	NP_004012.1:p.Gln548Arg
NM_004022.2:c.1643A>G	NP_004013.1:p.Gln548Arg
NM_004023.2:c.1643A>G	NP_004014.1:p.Gln548Arg
XM_006724468.2:c.9023A>G	XP_006724531.1:p.Gln3008Arg
XM_006724469.2:c.8999A>G	XP_006724532.1:p.Gln3000Arg
XM_006724470.2:c.9023A>G	XP_006724533.1:p.Gln3008Arg
XM_006724471.2:c.9023A>G	XP_006724534.1:p.Gln3008Arg
XM_006724472.2:c.8894A>G	XP_006724535.1:p.Gln2965Arg
XM_006724473.2:c.8885A>G	XP_006724536.1:p.Gln2962Arg
XM_006724474.2:c.9023A>G	XP_006724537.1:p.Gln3008Arg
XM_006724475.2:c.9023A>G	XP_006724538.1:p.Gln3008Arg
XM_011545467.1:c.8900A>G	XP_011543769.1:p.Gln2967Arg
XM_011545468.1:c.9023A>G	XP_011543770.1:p.Gln3008Arg
XM_006724469.3:c.8999A>G	XP_006724532.1:p.Gln3000Arg
XM_006724470.3:c.9023A>G	XP_006724533.1:p.Gln3008Arg
XM_006724474.3:c.9023A>G	XP_006724537.1:p.Gln3008Arg
XM_011545468.2:c.9023A>G	XP_011543770.1:p.Gln3008Arg
XM_017029328.1:c.9023A>G	XP_016884817.1:p.Gln3008Arg
XM_017029331.1:c.3197A>G	XP_016884820.1:p.Gln1066Arg
NM_000109.4:c.8999A>G	NP_000100.3:p.Gln3000Arg
NM_004006.3:c.9023A>G MANE Select	NP_003997.2:p.Gln3008Arg
NM_004011.4:c.5000A>G	NP_004002.3:p.Gln1667Arg
NM_004012.4:c.4991A>G	NP_004003.2:p.Gln1664Arg
NM_004021.3:c.1643A>G	NP_004012.2:p.Gln548Arg
NM_004023.3:c.1643A>G	NP_004014.2:p.Gln548Arg
NM_004013.3:c.1643A>G	NP_004004.2:p.Gln548Arg
NM_004014.3:c.836A>G	NP_004005.2:p.Gln279Arg
NM_004020.4:c.1643A>G	NP_004011.3:p.Gln548Arg
NM_004022.3:c.1643A>G	NP_004013.2:p.Gln548Arg