Canonical Allele Identifier: CA412654287

Gene: DMD

Linked Data

• dbSNP Id: rs41305353
• MyVariant Identifiers: chrX:g.31496431T>C (hg19) ; chrX:g.31478314T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31478314T>C , CM000685.2:g.31478314T>C	GRCh38
NC_000023.10:g.31496431T>C , CM000685.1:g.31496431T>C	GRCh37
NC_000023.9:g.31406352T>C	NCBI36
NG_012232.1:g.1866296A>G , LRG_199:g.1866296A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000358062.7:c.3575A>G	ENSP00000350765.3:p.Glu1192Gly
ENST00000682238.1:c.1349A>G	ENSP00000508124.1:p.Glu450Gly
ENST00000683450.1:n.2194A>G
ENST00000683957.1:n.2221A>G
ENST00000684130.1:c.1349A>G	ENSP00000508037.1:p.Glu450Gly
ENST00000343523.7:c.584A>G	ENSP00000340057.4:p.Glu195Gly
ENST00000357033.9:c.8729A>G MANE Select	ENSP00000354923.3:p.Glu2910Gly
ENST00000619831.5:c.4697A>G	ENSP00000479270.2:p.Glu1566Gly
ENST00000620040.5:c.1349A>G	ENSP00000478150.2:p.Glu450Gly
ENST00000680961.1:c.1349A>G	ENSP00000506386.1:p.Glu450Gly
ENST00000681646.1:n.2390A>G
ENST00000343523.6:c.542A>G	ENSP00000340057.3:p.Glu181Gly
ENST00000357033.8:c.8729A>G	ENSP00000354923.3:p.Glu2910Gly
ENST00000358062.6:c.1817A>G	ENSP00000350765.2:p.Glu606Gly
ENST00000359836.5:c.1349A>G	ENSP00000352894.1:p.Glu450Gly
ENST00000378677.6:c.8717A>G	ENSP00000367948.2:p.Glu2906Gly
ENST00000378707.7:c.1349A>G	ENSP00000367979.3:p.Glu450Gly
ENST00000474231.5:c.1349A>G	ENSP00000417123.1:p.Glu450Gly
ENST00000541735.5:c.1349A>G	ENSP00000444119.1:p.Glu450Gly
ENST00000619831.4:c.8714A>G	ENSP00000479270.1:p.Glu2905Gly
ENST00000620040.4:c.8726A>G	ENSP00000478150.1:p.Glu2909Gly
NM_000109.3:c.8705A>G	NP_000100.2:p.Glu2902Gly
NM_004006.2:c.8729A>G , LRG_199t1:c.8729A>G	NP_003997.1:p.Glu2910Gly
NM_004009.3:c.8717A>G	NP_004000.1:p.Glu2906Gly
NM_004010.3:c.8360A>G	NP_004001.1:p.Glu2787Gly
NM_004011.3:c.4706A>G	NP_004002.2:p.Glu1569Gly
NM_004012.3:c.4697A>G	NP_004003.1:p.Glu1566Gly
NM_004013.2:c.1349A>G	NP_004004.1:p.Glu450Gly
NM_004014.2:c.542A>G	NP_004005.1:p.Glu181Gly
NM_004020.3:c.1349A>G	NP_004011.2:p.Glu450Gly
NM_004021.2:c.1349A>G	NP_004012.1:p.Glu450Gly
NM_004022.2:c.1349A>G	NP_004013.1:p.Glu450Gly
NM_004023.2:c.1349A>G	NP_004014.1:p.Glu450Gly
XM_006724468.2:c.8729A>G	XP_006724531.1:p.Glu2910Gly
XM_006724469.2:c.8705A>G	XP_006724532.1:p.Glu2902Gly
XM_006724470.2:c.8729A>G	XP_006724533.1:p.Glu2910Gly
XM_006724471.2:c.8729A>G	XP_006724534.1:p.Glu2910Gly
XM_006724472.2:c.8600A>G	XP_006724535.1:p.Glu2867Gly
XM_006724473.2:c.8591A>G	XP_006724536.1:p.Glu2864Gly
XM_006724474.2:c.8729A>G	XP_006724537.1:p.Glu2910Gly
XM_006724475.2:c.8729A>G	XP_006724538.1:p.Glu2910Gly
XM_011545467.1:c.8606A>G	XP_011543769.1:p.Glu2869Gly
XM_011545468.1:c.8729A>G	XP_011543770.1:p.Glu2910Gly
XM_006724469.3:c.8705A>G	XP_006724532.1:p.Glu2902Gly
XM_006724470.3:c.8729A>G	XP_006724533.1:p.Glu2910Gly
XM_006724474.3:c.8729A>G	XP_006724537.1:p.Glu2910Gly
XM_011545468.2:c.8729A>G	XP_011543770.1:p.Glu2910Gly
XM_017029328.1:c.8729A>G	XP_016884817.1:p.Glu2910Gly
XM_017029331.1:c.2903A>G	XP_016884820.1:p.Glu968Gly
NM_000109.4:c.8705A>G	NP_000100.3:p.Glu2902Gly
NM_004006.3:c.8729A>G MANE Select	NP_003997.2:p.Glu2910Gly
NM_004011.4:c.4706A>G	NP_004002.3:p.Glu1569Gly
NM_004012.4:c.4697A>G	NP_004003.2:p.Glu1566Gly
NM_004021.3:c.1349A>G	NP_004012.2:p.Glu450Gly
NM_004023.3:c.1349A>G	NP_004014.2:p.Glu450Gly
NM_004013.3:c.1349A>G	NP_004004.2:p.Glu450Gly
NM_004014.3:c.542A>G	NP_004005.2:p.Glu181Gly
NM_004020.4:c.1349A>G	NP_004011.3:p.Glu450Gly
NM_004022.3:c.1349A>G	NP_004013.2:p.Glu450Gly