Canonical Allele Identifier: CA412674811

Gene: DMD

Linked Data

• ClinVar Variation Id: 455870
• ClinVar RCV Id: RCV000549989
• dbSNP Id: rs1557084067
• MyVariant Identifiers: chrX:g.32867844C>T (hg19) ; chrX:g.32849727C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32849727C>T , CM000685.2:g.32849727C>T	GRCh38
NC_000023.10:g.32867844C>T , CM000685.1:g.32867844C>T	GRCh37
NC_000023.9:g.32777765C>T	NCBI36
NG_012232.1:g.494883G>A , LRG_199:g.494883G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682071.1:c.-184+1G>A	ENSP00000508133.1:n.-184+1G>A
ENST00000682437.1:n.510+1G>A
ENST00000682584.1:n.510+1G>A
ENST00000682870.1:n.371+1G>A
ENST00000682899.1:n.393+1G>A
ENST00000682924.1:c.186+1G>A	ENSP00000508187.1:n.186+1G>A
ENST00000683309.1:n.370+1G>A
ENST00000683658.1:n.531+1G>A
ENST00000683985.1:n.393+1G>A
ENST00000684056.1:n.370+1G>A
ENST00000684165.1:n.393+1G>A
ENST00000684237.1:c.186+1G>A	ENSP00000507277.1:n.186+1G>A
ENST00000684292.1:n.393+1G>A
ENST00000684357.1:n.370+1G>A
ENST00000684660.1:n.371+1G>A
ENST00000288447.9:c.162+1G>A	ENSP00000288447.4:n.162+1G>A
ENST00000357033.9:c.186+1G>A MANE Select	ENSP00000354923.3:n.186+1G>A
ENST00000288447.8:c.162+1G>A	ENSP00000288447.4:n.162+1G>A
ENST00000357033.8:c.186+1G>A	ENSP00000354923.3:n.186+1G>A
ENST00000378677.6:c.174+1G>A	ENSP00000367948.2:n.174+1G>A
ENST00000420596.5:c.93+170412G>A	ENSP00000399897.1:n.93+170412G>A
ENST00000447523.1:c.75+1G>A	ENSP00000395904.1:n.75+1G>A
ENST00000448370.5:c.93+170412G>A	ENSP00000388559.1:n.93+170412G>A
ENST00000488902.5:n.335+170412G>A
ENST00000619831.4:c.174+1G>A	ENSP00000479270.1:n.174+1G>A
ENST00000620040.4:c.186+1G>A	ENSP00000478150.1:n.186+1G>A
NM_000109.3:c.162+1G>A	NP_000100.2:n.162+1G>A
NM_004006.2:c.186+1G>A , LRG_199t1:c.186+1G>A	NP_003997.1:n.186+1G>A
NM_004009.3:c.174+1G>A	NP_004000.1:n.174+1G>A
NM_004010.3:c.-184+1G>A	NP_004001.1:n.-184+1G>A
XM_006724468.2:c.186+1G>A	XP_006724531.1:n.186+1G>A
XM_006724469.2:c.162+1G>A	XP_006724532.1:n.162+1G>A
XM_006724470.2:c.186+1G>A	XP_006724533.1:n.186+1G>A
XM_006724471.2:c.186+1G>A	XP_006724534.1:n.186+1G>A
XM_006724472.2:c.186+1G>A	XP_006724535.1:n.186+1G>A
XM_006724473.2:c.186+1G>A	XP_006724536.1:n.186+1G>A
XM_006724474.2:c.186+1G>A	XP_006724537.1:n.186+1G>A
XM_006724475.2:c.186+1G>A	XP_006724538.1:n.186+1G>A
XM_011545467.1:c.186+1G>A	XP_011543769.1:n.186+1G>A
XM_011545468.1:c.186+1G>A	XP_011543770.1:n.186+1G>A
XM_011545469.1:c.186+1G>A	XP_011543771.1:n.186+1G>A
XM_006724469.3:c.162+1G>A	XP_006724532.1:n.162+1G>A
XM_006724470.3:c.186+1G>A	XP_006724533.1:n.186+1G>A
XM_006724474.3:c.186+1G>A	XP_006724537.1:n.186+1G>A
XM_011545468.2:c.186+1G>A	XP_011543770.1:n.186+1G>A
XM_017029328.1:c.186+1G>A	XP_016884817.1:n.186+1G>A
XM_017029329.1:c.186+1G>A	XP_016884818.1:n.186+1G>A
XM_017029330.2:c.186+1G>A	XP_016884819.1:n.186+1G>A
NM_000109.4:c.162+1G>A	NP_000100.3:n.162+1G>A
NM_004006.3:c.186+1G>A MANE Select	NP_003997.2:n.186+1G>A