Canonical Allele Identifier: CA412663580

Gene: DMD

Linked Data

• ClinVar Variation Id: 495113
• ClinVar RCV Id: RCV000585714
• dbSNP Id: rs1557396600
• MyVariant Identifiers: chrX:g.32536123A>C (hg19) ; chrX:g.32518006A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32518006A>C , CM000685.2:g.32518006A>C	GRCh38
NC_000023.10:g.32536123A>C , CM000685.1:g.32536123A>C	GRCh37
NC_000023.9:g.32446044A>C	NCBI36
NG_012232.1:g.826604T>G , LRG_199:g.826604T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682899.1:n.2499+2T>G
ENST00000683985.1:n.2499+2T>G
ENST00000288447.9:c.2270T>G	ENSP00000288447.4:p.Val757Gly
ENST00000357033.9:c.2292+2T>G MANE Select	ENSP00000354923.3:n.2292+2T>G
ENST00000288447.8:c.2270T>G	ENSP00000288447.4:p.Val757Gly
ENST00000357033.8:c.2292+2T>G	ENSP00000354923.3:n.2292+2T>G
ENST00000378677.6:c.2280+2T>G	ENSP00000367948.2:n.2280+2T>G
ENST00000420596.5:c.94-152807T>G	ENSP00000399897.1:n.94-152807T>G
ENST00000448370.5:c.94-153296T>G	ENSP00000388559.1:n.94-153296T>G
ENST00000488902.5:n.336-300943T>G
ENST00000619831.4:c.2280+2T>G	ENSP00000479270.1:n.2280+2T>G
ENST00000620040.4:c.2292+2T>G	ENSP00000478150.1:n.2292+2T>G
NM_000109.3:c.2268+2T>G	NP_000100.2:n.2268+2T>G
NM_004006.2:c.2292+2T>G , LRG_199t1:c.2292+2T>G	NP_003997.1:n.2292+2T>G
NM_004009.3:c.2280+2T>G	NP_004000.1:n.2280+2T>G
NM_004010.3:c.1923+2T>G	NP_004001.1:n.1923+2T>G
XM_006724468.2:c.2292+2T>G	XP_006724531.1:n.2292+2T>G
XM_006724469.2:c.2268+2T>G	XP_006724532.1:n.2268+2T>G
XM_006724470.2:c.2292+2T>G	XP_006724533.1:n.2292+2T>G
XM_006724471.2:c.2292+2T>G	XP_006724534.1:n.2292+2T>G
XM_006724472.2:c.2163+2T>G	XP_006724535.1:n.2163+2T>G
XM_006724473.2:c.2292+2T>G	XP_006724536.1:n.2292+2T>G
XM_006724474.2:c.2292+2T>G	XP_006724537.1:n.2292+2T>G
XM_006724475.2:c.2292+2T>G	XP_006724538.1:n.2292+2T>G
XM_011545467.1:c.2292+2T>G	XP_011543769.1:n.2292+2T>G
XM_011545468.1:c.2292+2T>G	XP_011543770.1:n.2292+2T>G
XM_011545469.1:c.2292+2T>G	XP_011543771.1:n.2292+2T>G
XM_006724469.3:c.2268+2T>G	XP_006724532.1:n.2268+2T>G
XM_006724470.3:c.2292+2T>G	XP_006724533.1:n.2292+2T>G
XM_006724474.3:c.2292+2T>G	XP_006724537.1:n.2292+2T>G
XM_011545468.2:c.2292+2T>G	XP_011543770.1:n.2292+2T>G
XM_017029328.1:c.2292+2T>G	XP_016884817.1:n.2292+2T>G
XM_017029329.1:c.2292+2T>G	XP_016884818.1:n.2292+2T>G
XM_017029330.2:c.2292+2T>G	XP_016884819.1:n.2292+2T>G
NM_000109.4:c.2268+2T>G	NP_000100.3:n.2268+2T>G
NM_004006.3:c.2292+2T>G MANE Select	NP_003997.2:n.2292+2T>G