Canonical Allele Identifier: CA2739273453

Gene: DMD

Linked Data

• ClinVar Variation Id: 2829882
• ClinVar RCV Id: RCV003622892

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32365020del , CM000685.2:g.32365020del	GRCh38
NC_000023.10:g.32383137del , CM000685.1:g.32383137del	GRCh37
NC_000023.9:g.32293058del	NCBI36
NG_012232.1:g.979591del , LRG_199:g.979591del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357033.9:c.5025+1del
ENST00000619831.5:c.993+1del
ENST00000357033.8:c.5025+1del
ENST00000378677.6:c.5013+1del
ENST00000420596.5:c.273+1del
ENST00000448370.5:c.94-309del	ENSP00000388559.1:n.94-309del
ENST00000488902.5:n.336-147956del
ENST00000619831.4:c.5013+1del
ENST00000620040.4:c.5025+1del
NM_000109.3:c.5001+1del
NM_004006.2:c.5025+1del , LRG_199t1:c.5025+1del
NM_004009.3:c.5013+1del
NM_004010.3:c.4656+1del
NM_004011.3:c.1002+1del
NM_004012.3:c.993+1del
XM_006724468.2:c.5025+1del
XM_006724469.2:c.5001+1del
XM_006724470.2:c.5025+1del
XM_006724471.2:c.5025+1del
XM_006724472.2:c.4896+1del
XM_006724473.2:c.5025+1del
XM_006724474.2:c.5025+1del
XM_006724475.2:c.5025+1del
XM_011545467.1:c.5025+1del
XM_011545468.1:c.5025+1del
XM_011545469.1:c.5025+1del
XM_006724469.3:c.5001+1del
XM_006724470.3:c.5025+1del
XM_006724474.3:c.5025+1del
XM_011545468.2:c.5025+1del
XM_017029328.1:c.5025+1del
XM_017029329.1:c.5025+1del
XM_017029330.2:c.5025+1del
NM_000109.4:c.5001+1del
NM_004006.3:c.5025+1del
NM_004011.4:c.1002+1del
NM_004012.4:c.993+1del