Canonical Allele Identifier: CA2579580148

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32573706_32573708dup , CM000685.2:g.32573706_32573708dup	GRCh38
NC_000023.10:g.32591823_32591825dup , CM000685.1:g.32591823_32591825dup	GRCh37
NC_000023.9:g.32501744_32501746dup	NCBI36
NG_012232.1:g.770905_770907dup , LRG_199:g.770905_770907dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682071.1:c.1335+40_1335+42dup	ENSP00000508133.1:n.1335+40_1335+42dup
ENST00000682899.1:n.1911+40_1911+42dup
ENST00000682924.1:c.*203+40_*203+42dup	ENSP00000508187.1:n.*203+40_*203+42dup
ENST00000683985.1:n.1911+40_1911+42dup
ENST00000684165.1:n.1911+40_1911+42dup
ENST00000684292.1:n.1911+40_1911+42dup
ENST00000288447.9:c.1680+40_1680+42dup	ENSP00000288447.4:n.1680+40_1680+42dup
ENST00000357033.9:c.1704+40_1704+42dup MANE Select	ENSP00000354923.3:n.1704+40_1704+42dup
ENST00000288447.8:c.1680+40_1680+42dup	ENSP00000288447.4:n.1680+40_1680+42dup
ENST00000357033.8:c.1704+40_1704+42dup	ENSP00000354923.3:n.1704+40_1704+42dup
ENST00000378677.6:c.1692+40_1692+42dup	ENSP00000367948.2:n.1692+40_1692+42dup
ENST00000420596.5:c.94-208506_94-208504dup	ENSP00000399897.1:n.94-208506_94-208504dup
ENST00000447523.1:c.348+40_348+42dup	ENSP00000395904.1:n.348+40_348+42dup
ENST00000448370.5:c.94-208995_94-208993dup	ENSP00000388559.1:n.94-208995_94-208993dup
ENST00000480751.1:n.188+40_188+42dup
ENST00000488902.5:n.336-356642_336-356640dup
ENST00000619831.4:c.1692+40_1692+42dup	ENSP00000479270.1:n.1692+40_1692+42dup
ENST00000620040.4:c.1704+40_1704+42dup	ENSP00000478150.1:n.1704+40_1704+42dup
NM_000109.3:c.1680+40_1680+42dup	NP_000100.2:n.1680+40_1680+42dup
NM_004006.2:c.1704+40_1704+42dup , LRG_199t1:c.1704+40_1704+42dup	NP_003997.1:n.1704+40_1704+42dup
NM_004009.3:c.1692+40_1692+42dup	NP_004000.1:n.1692+40_1692+42dup
NM_004010.3:c.1335+40_1335+42dup	NP_004001.1:n.1335+40_1335+42dup
XM_006724468.2:c.1704+40_1704+42dup	XP_006724531.1:n.1704+40_1704+42dup
XM_006724469.2:c.1680+40_1680+42dup	XP_006724532.1:n.1680+40_1680+42dup
XM_006724470.2:c.1704+40_1704+42dup	XP_006724533.1:n.1704+40_1704+42dup
XM_006724471.2:c.1704+40_1704+42dup	XP_006724534.1:n.1704+40_1704+42dup
XM_006724472.2:c.1575+40_1575+42dup	XP_006724535.1:n.1575+40_1575+42dup
XM_006724473.2:c.1704+40_1704+42dup	XP_006724536.1:n.1704+40_1704+42dup
XM_006724474.2:c.1704+40_1704+42dup	XP_006724537.1:n.1704+40_1704+42dup
XM_006724475.2:c.1704+40_1704+42dup	XP_006724538.1:n.1704+40_1704+42dup
XM_011545467.1:c.1704+40_1704+42dup	XP_011543769.1:n.1704+40_1704+42dup
XM_011545468.1:c.1704+40_1704+42dup	XP_011543770.1:n.1704+40_1704+42dup
XM_011545469.1:c.1704+40_1704+42dup	XP_011543771.1:n.1704+40_1704+42dup
XM_006724469.3:c.1680+40_1680+42dup	XP_006724532.1:n.1680+40_1680+42dup
XM_006724470.3:c.1704+40_1704+42dup	XP_006724533.1:n.1704+40_1704+42dup
XM_006724474.3:c.1704+40_1704+42dup	XP_006724537.1:n.1704+40_1704+42dup
XM_011545468.2:c.1704+40_1704+42dup	XP_011543770.1:n.1704+40_1704+42dup
XM_017029328.1:c.1704+40_1704+42dup	XP_016884817.1:n.1704+40_1704+42dup
XM_017029329.1:c.1704+40_1704+42dup	XP_016884818.1:n.1704+40_1704+42dup
XM_017029330.2:c.1704+40_1704+42dup	XP_016884819.1:n.1704+40_1704+42dup
NM_000109.4:c.1680+40_1680+42dup	NP_000100.3:n.1680+40_1680+42dup
NM_004006.3:c.1704+40_1704+42dup MANE Select	NP_003997.2:n.1704+40_1704+42dup