Canonical Allele Identifier: CA2422736430

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32287613_32287614delinsAC , CM000685.2:g.32287613_32287614delinsAC	GRCh38
NC_000023.10:g.32305730_32305731delinsAC , CM000685.1:g.32305730_32305731delinsAC	GRCh37
NC_000023.9:g.32215651_32215652delinsAC	NCBI36
NG_012232.1:g.1056996_1056997delinsGT , LRG_199:g.1056996_1056997delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.1051_1052delinsGT	ENSP00000350765.3:p.Val351=
ENST00000357033.9:c.6205_6206delinsGT MANE Select	ENSP00000354923.3:p.Val2069=
ENST00000619831.5:c.2173_2174delinsGT	ENSP00000479270.2:p.Val725=
ENST00000357033.8:c.6205_6206delinsGT	ENSP00000354923.3:p.Val2069=
ENST00000378677.6:c.6193_6194delinsGT	ENSP00000367948.2:p.Val2065=
ENST00000488902.5:n.336-70551_336-70550delinsGT
ENST00000619831.4:c.6193_6194delinsGT	ENSP00000479270.1:p.Val2065=
ENST00000620040.4:c.6205_6206delinsGT	ENSP00000478150.1:p.Val2069=
NM_000109.3:c.6181_6182delinsGT	NP_000100.2:p.Val2061=
NM_004006.2:c.6205_6206delinsGT , LRG_199t1:c.6205_6206delinsGT	NP_003997.1:p.Val2069=
NM_004009.3:c.6193_6194delinsGT	NP_004000.1:p.Val2065=
NM_004010.3:c.5836_5837delinsGT	NP_004001.1:p.Val1946=
NM_004011.3:c.2182_2183delinsGT	NP_004002.2:p.Val728=
NM_004012.3:c.2173_2174delinsGT	NP_004003.1:p.Val725=
XM_006724468.2:c.6205_6206delinsGT	XP_006724531.1:p.Val2069=
XM_006724469.2:c.6181_6182delinsGT	XP_006724532.1:p.Val2061=
XM_006724470.2:c.6205_6206delinsGT	XP_006724533.1:p.Val2069=
XM_006724471.2:c.6205_6206delinsGT	XP_006724534.1:p.Val2069=
XM_006724472.2:c.6076_6077delinsGT	XP_006724535.1:p.Val2026=
XM_006724473.2:c.6067_6068delinsGT	XP_006724536.1:p.Val2023=
XM_006724474.2:c.6205_6206delinsGT	XP_006724537.1:p.Val2069=
XM_006724475.2:c.6205_6206delinsGT	XP_006724538.1:p.Val2069=
XM_011545467.1:c.6082_6083delinsGT	XP_011543769.1:p.Val2028=
XM_011545468.1:c.6205_6206delinsGT	XP_011543770.1:p.Val2069=
XM_006724469.3:c.6181_6182delinsGT	XP_006724532.1:p.Val2061=
XM_006724470.3:c.6205_6206delinsGT	XP_006724533.1:p.Val2069=
XM_006724474.3:c.6205_6206delinsGT	XP_006724537.1:p.Val2069=
XM_011545468.2:c.6205_6206delinsGT	XP_011543770.1:p.Val2069=
XM_017029328.1:c.6205_6206delinsGT	XP_016884817.1:p.Val2069=
XM_017029329.1:c.6205_6206delinsGT	XP_016884818.1:p.Val2069=
XM_017029330.2:c.6205_6206delinsGT	XP_016884819.1:p.Val2069=
XM_017029331.1:c.379_380delinsGT	XP_016884820.1:p.Val127=
NM_000109.4:c.6181_6182delinsGT	NP_000100.3:p.Val2061=
NM_004006.3:c.6205_6206delinsGT MANE Select	NP_003997.2:p.Val2069=
NM_004011.4:c.2182_2183delinsGT	NP_004002.3:p.Val728=
NM_004012.4:c.2173_2174delinsGT	NP_004003.2:p.Val725=