Canonical Allele Identifier: CA10604295

Gene: DMD

Linked Data

• ClinVar Variation Id: 282785
• ClinVar RCV Id: RCV000328785
• dbSNP Id: rs886042480
• MyVariant Identifiers: chrX:g.32715980G>C (hg19) ; chrX:g.32697863G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32697863G>C , CM000685.2:g.32697863G>C	GRCh38
NC_000023.10:g.32715980G>C , CM000685.1:g.32715980G>C	GRCh37
NC_000023.9:g.32625901G>C	NCBI36
NG_012232.1:g.646747C>G , LRG_199:g.646747C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682071.1:c.591+7C>G	ENSP00000508133.1:n.591+7C>G
ENST00000682870.1:n.1152C>G
ENST00000682899.1:n.1167+7C>G
ENST00000682924.1:c.960+7C>G	ENSP00000508187.1:n.960+7C>G
ENST00000683985.1:n.1167+7C>G
ENST00000684165.1:n.1167+7C>G
ENST00000684237.1:c.831+1249C>G	ENSP00000507277.1:n.831+1249C>G
ENST00000684292.1:n.1167+7C>G
ENST00000288447.9:c.936+7C>G	ENSP00000288447.4:n.936+7C>G
ENST00000357033.9:c.960+7C>G MANE Select	ENSP00000354923.3:n.960+7C>G
ENST00000288447.8:c.936+7C>G	ENSP00000288447.4:n.936+7C>G
ENST00000357033.8:c.960+7C>G	ENSP00000354923.3:n.960+7C>G
ENST00000378677.6:c.948+7C>G	ENSP00000367948.2:n.948+7C>G
ENST00000420596.5:c.93+322276C>G	ENSP00000399897.1:n.93+322276C>G
ENST00000447523.1:c.247-124017C>G	ENSP00000395904.1:n.247-124017C>G
ENST00000448370.5:c.93+322276C>G	ENSP00000388559.1:n.93+322276C>G
ENST00000480751.1:n.86+118605C>G
ENST00000488902.5:n.335+322276C>G
ENST00000619831.4:c.948+7C>G	ENSP00000479270.1:n.948+7C>G
ENST00000620040.4:c.960+7C>G	ENSP00000478150.1:n.960+7C>G
NM_000109.3:c.936+7C>G	NP_000100.2:n.936+7C>G
NM_004006.2:c.960+7C>G , LRG_199t1:c.960+7C>G	NP_003997.1:n.960+7C>G
NM_004009.3:c.948+7C>G	NP_004000.1:n.948+7C>G
NM_004010.3:c.591+7C>G	NP_004001.1:n.591+7C>G
XM_006724468.2:c.960+7C>G	XP_006724531.1:n.960+7C>G
XM_006724469.2:c.936+7C>G	XP_006724532.1:n.936+7C>G
XM_006724470.2:c.960+7C>G	XP_006724533.1:n.960+7C>G
XM_006724471.2:c.960+7C>G	XP_006724534.1:n.960+7C>G
XM_006724472.2:c.831+1249C>G	XP_006724535.1:n.831+1249C>G
XM_006724473.2:c.960+7C>G	XP_006724536.1:n.960+7C>G
XM_006724474.2:c.960+7C>G	XP_006724537.1:n.960+7C>G
XM_006724475.2:c.960+7C>G	XP_006724538.1:n.960+7C>G
XM_011545467.1:c.960+7C>G	XP_011543769.1:n.960+7C>G
XM_011545468.1:c.960+7C>G	XP_011543770.1:n.960+7C>G
XM_011545469.1:c.960+7C>G	XP_011543771.1:n.960+7C>G
XM_006724469.3:c.936+7C>G	XP_006724532.1:n.936+7C>G
XM_006724470.3:c.960+7C>G	XP_006724533.1:n.960+7C>G
XM_006724474.3:c.960+7C>G	XP_006724537.1:n.960+7C>G
XM_011545468.2:c.960+7C>G	XP_011543770.1:n.960+7C>G
XM_017029328.1:c.960+7C>G	XP_016884817.1:n.960+7C>G
XM_017029329.1:c.960+7C>G	XP_016884818.1:n.960+7C>G
XM_017029330.2:c.960+7C>G	XP_016884819.1:n.960+7C>G
NM_000109.4:c.936+7C>G	NP_000100.3:n.936+7C>G
NM_004006.3:c.960+7C>G MANE Select	NP_003997.2:n.960+7C>G