Canonical Allele Identifier: CA2695232737

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32343148_32343152delinsATTTTCCTAC , CM000685.2:g.32343148_32343152delinsATTTTCCTAC	GRCh38
NC_000023.10:g.32361265_32361269delinsATTTTCCTAC , CM000685.1:g.32361265_32361269delinsATTTTCCTAC	GRCh37
NC_000023.9:g.32271186_32271190delinsATTTTCCTAC	NCBI36
NG_012232.1:g.1001458_1001462delinsGTAGGAAAAT , LRG_199:g.1001458_1001462delinsGTAGGAAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.567_571delinsGTAGGAAAAT	ENSP00000350765.3:p.Asp190Ter
ENST00000357033.9:c.5721_5725delinsGTAGGAAAAT MANE Select	ENSP00000354923.3:p.Asp1908Ter
ENST00000619831.5:c.1689_1693delinsGTAGGAAAAT	ENSP00000479270.2:p.Asp564Ter
ENST00000357033.8:c.5721_5725delinsGTAGGAAAAT	ENSP00000354923.3:p.Asp1908Ter
ENST00000378677.6:c.5709_5713delinsGTAGGAAAAT	ENSP00000367948.2:p.Asp1904Ter
ENST00000488902.5:n.336-126089_336-126085delinsGTAGGAAAAT
ENST00000493412.1:c.378_382delinsGTAGGAAAAT	ENSP00000417725.1:p.Asp127Ter
ENST00000619831.4:c.5709_5713delinsGTAGGAAAAT	ENSP00000479270.1:p.Asp1904Ter
ENST00000620040.4:c.5721_5725delinsGTAGGAAAAT	ENSP00000478150.1:p.Asp1908Ter
NM_000109.3:c.5697_5701delinsGTAGGAAAAT	NP_000100.2:p.Asp1900Ter
NM_004006.2:c.5721_5725delinsGTAGGAAAAT , LRG_199t1:c.5721_5725delinsGTAGGAAAAT	NP_003997.1:p.Asp1908Ter
NM_004009.3:c.5709_5713delinsGTAGGAAAAT	NP_004000.1:p.Asp1904Ter
NM_004010.3:c.5352_5356delinsGTAGGAAAAT	NP_004001.1:p.Asp1785Ter
NM_004011.3:c.1698_1702delinsGTAGGAAAAT	NP_004002.2:p.Asp567Ter
NM_004012.3:c.1689_1693delinsGTAGGAAAAT	NP_004003.1:p.Asp564Ter
XM_006724468.2:c.5721_5725delinsGTAGGAAAAT	XP_006724531.1:p.Asp1908Ter
XM_006724469.2:c.5697_5701delinsGTAGGAAAAT	XP_006724532.1:p.Asp1900Ter
XM_006724470.2:c.5721_5725delinsGTAGGAAAAT	XP_006724533.1:p.Asp1908Ter
XM_006724471.2:c.5721_5725delinsGTAGGAAAAT	XP_006724534.1:p.Asp1908Ter
XM_006724472.2:c.5592_5596delinsGTAGGAAAAT	XP_006724535.1:p.Asp1865Ter
XM_006724473.2:c.5583_5587delinsGTAGGAAAAT	XP_006724536.1:p.Asp1862Ter
XM_006724474.2:c.5721_5725delinsGTAGGAAAAT	XP_006724537.1:p.Asp1908Ter
XM_006724475.2:c.5721_5725delinsGTAGGAAAAT	XP_006724538.1:p.Asp1908Ter
XM_011545467.1:c.5598_5602delinsGTAGGAAAAT	XP_011543769.1:p.Asp1867Ter
XM_011545468.1:c.5721_5725delinsGTAGGAAAAT	XP_011543770.1:p.Asp1908Ter
XM_011545469.1:c.5721_5725delinsGTAGGAAAAT	XP_011543771.1:p.Asp1908Ter
XM_006724469.3:c.5697_5701delinsGTAGGAAAAT	XP_006724532.1:p.Asp1900Ter
XM_006724470.3:c.5721_5725delinsGTAGGAAAAT	XP_006724533.1:p.Asp1908Ter
XM_006724474.3:c.5721_5725delinsGTAGGAAAAT	XP_006724537.1:p.Asp1908Ter
XM_011545468.2:c.5721_5725delinsGTAGGAAAAT	XP_011543770.1:p.Asp1908Ter
XM_017029328.1:c.5721_5725delinsGTAGGAAAAT	XP_016884817.1:p.Asp1908Ter
XM_017029329.1:c.5721_5725delinsGTAGGAAAAT	XP_016884818.1:p.Asp1908Ter
XM_017029330.2:c.5721_5725delinsGTAGGAAAAT	XP_016884819.1:p.Asp1908Ter
NM_000109.4:c.5697_5701delinsGTAGGAAAAT	NP_000100.3:p.Asp1900Ter
NM_004006.3:c.5721_5725delinsGTAGGAAAAT MANE Select	NP_003997.2:p.Asp1908Ter
NM_004011.4:c.1698_1702delinsGTAGGAAAAT	NP_004002.3:p.Asp567Ter
NM_004012.4:c.1689_1693delinsGTAGGAAAAT	NP_004003.2:p.Asp564Ter