Canonical Allele Identifier: CA412667538

Gene: DMD

Linked Data

• ClinVar Variation Id: 929016
• ClinVar RCV Id: RCV001193795
• dbSNP Id: rs1064796764
• MyVariant Identifiers: chrX:g.32366522C>A (hg19) ; chrX:g.32348405C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32348405C>A , CM000685.2:g.32348405C>A	GRCh38
NC_000023.10:g.32366522C>A , CM000685.1:g.32366522C>A	GRCh37
NC_000023.9:g.32276443C>A	NCBI36
NG_012232.1:g.996205G>T , LRG_199:g.996205G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000358062.7:c.294+1G>T	ENSP00000350765.3:n.294+1G>T
ENST00000357033.9:c.5448+1G>T MANE Select	ENSP00000354923.3:n.5448+1G>T
ENST00000619831.5:c.1416+1G>T	ENSP00000479270.2:n.1416+1G>T
ENST00000357033.8:c.5448+1G>T	ENSP00000354923.3:n.5448+1G>T
ENST00000378677.6:c.5436+1G>T	ENSP00000367948.2:n.5436+1G>T
ENST00000488902.5:n.336-131342G>T
ENST00000493412.1:c.105+1G>T	ENSP00000417725.1:n.105+1G>T
ENST00000619831.4:c.5436+1G>T	ENSP00000479270.1:n.5436+1G>T
ENST00000620040.4:c.5448+1G>T	ENSP00000478150.1:n.5448+1G>T
NM_000109.3:c.5424+1G>T	NP_000100.2:n.5424+1G>T
NM_004006.2:c.5448+1G>T , LRG_199t1:c.5448+1G>T	NP_003997.1:n.5448+1G>T
NM_004009.3:c.5436+1G>T	NP_004000.1:n.5436+1G>T
NM_004010.3:c.5079+1G>T	NP_004001.1:n.5079+1G>T
NM_004011.3:c.1425+1G>T	NP_004002.2:n.1425+1G>T
NM_004012.3:c.1416+1G>T	NP_004003.1:n.1416+1G>T
XM_006724468.2:c.5448+1G>T	XP_006724531.1:n.5448+1G>T
XM_006724469.2:c.5424+1G>T	XP_006724532.1:n.5424+1G>T
XM_006724470.2:c.5448+1G>T	XP_006724533.1:n.5448+1G>T
XM_006724471.2:c.5448+1G>T	XP_006724534.1:n.5448+1G>T
XM_006724472.2:c.5319+1G>T	XP_006724535.1:n.5319+1G>T
XM_006724473.2:c.5448+1G>T	XP_006724536.1:n.5448+1G>T
XM_006724474.2:c.5448+1G>T	XP_006724537.1:n.5448+1G>T
XM_006724475.2:c.5448+1G>T	XP_006724538.1:n.5448+1G>T
XM_011545467.1:c.5326-2325G>T	XP_011543769.1:n.5326-2325G>T
XM_011545468.1:c.5448+1G>T	XP_011543770.1:n.5448+1G>T
XM_011545469.1:c.5448+1G>T	XP_011543771.1:n.5448+1G>T
XM_006724469.3:c.5424+1G>T	XP_006724532.1:n.5424+1G>T
XM_006724470.3:c.5448+1G>T	XP_006724533.1:n.5448+1G>T
XM_006724474.3:c.5448+1G>T	XP_006724537.1:n.5448+1G>T
XM_011545468.2:c.5448+1G>T	XP_011543770.1:n.5448+1G>T
XM_017029328.1:c.5448+1G>T	XP_016884817.1:n.5448+1G>T
XM_017029329.1:c.5448+1G>T	XP_016884818.1:n.5448+1G>T
XM_017029330.2:c.5448+1G>T	XP_016884819.1:n.5448+1G>T
NM_000109.4:c.5424+1G>T	NP_000100.3:n.5424+1G>T
NM_004006.3:c.5448+1G>T MANE Select	NP_003997.2:n.5448+1G>T
NM_004011.4:c.1425+1G>T	NP_004002.3:n.1425+1G>T
NM_004012.4:c.1416+1G>T	NP_004003.2:n.1416+1G>T