Canonical Allele Identifier: CA2422760768

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32343139_32343144delinsTTTTCC , CM000685.2:g.32343139_32343144delinsTTTTCC	GRCh38
NC_000023.10:g.32361256_32361261delinsTTTTCC , CM000685.1:g.32361256_32361261delinsTTTTCC	GRCh37
NC_000023.9:g.32271177_32271182delinsTTTTCC	NCBI36
NG_012232.1:g.1001466_1001471delinsGGAAAA , LRG_199:g.1001466_1001471delinsGGAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.575_580delinsGGAAAA	ENSP00000350765.3:p.Arg192=
ENST00000357033.9:c.5729_5734delinsGGAAAA MANE Select	ENSP00000354923.3:p.Arg1910=
ENST00000619831.5:c.1697_1702delinsGGAAAA	ENSP00000479270.2:p.Arg566=
ENST00000357033.8:c.5729_5734delinsGGAAAA	ENSP00000354923.3:p.Arg1910=
ENST00000378677.6:c.5717_5722delinsGGAAAA	ENSP00000367948.2:p.Arg1906=
ENST00000488902.5:n.336-126081_336-126076delinsGGAAAA
ENST00000493412.1:c.386_391delinsGGAAAA	ENSP00000417725.1:p.Arg129=
ENST00000619831.4:c.5717_5722delinsGGAAAA	ENSP00000479270.1:p.Arg1906=
ENST00000620040.4:c.5729_5734delinsGGAAAA	ENSP00000478150.1:p.Arg1910=
NM_000109.3:c.5705_5710delinsGGAAAA	NP_000100.2:p.Arg1902=
NM_004006.2:c.5729_5734delinsGGAAAA , LRG_199t1:c.5729_5734delinsGGAAAA	NP_003997.1:p.Arg1910=
NM_004009.3:c.5717_5722delinsGGAAAA	NP_004000.1:p.Arg1906=
NM_004010.3:c.5360_5365delinsGGAAAA	NP_004001.1:p.Arg1787=
NM_004011.3:c.1706_1711delinsGGAAAA	NP_004002.2:p.Arg569=
NM_004012.3:c.1697_1702delinsGGAAAA	NP_004003.1:p.Arg566=
XM_006724468.2:c.5729_5734delinsGGAAAA	XP_006724531.1:p.Arg1910=
XM_006724469.2:c.5705_5710delinsGGAAAA	XP_006724532.1:p.Arg1902=
XM_006724470.2:c.5729_5734delinsGGAAAA	XP_006724533.1:p.Arg1910=
XM_006724471.2:c.5729_5734delinsGGAAAA	XP_006724534.1:p.Arg1910=
XM_006724472.2:c.5600_5605delinsGGAAAA	XP_006724535.1:p.Arg1867=
XM_006724473.2:c.5591_5596delinsGGAAAA	XP_006724536.1:p.Arg1864=
XM_006724474.2:c.5729_5734delinsGGAAAA	XP_006724537.1:p.Arg1910=
XM_006724475.2:c.5729_5734delinsGGAAAA	XP_006724538.1:p.Arg1910=
XM_011545467.1:c.5606_5611delinsGGAAAA	XP_011543769.1:p.Arg1869=
XM_011545468.1:c.5729_5734delinsGGAAAA	XP_011543770.1:p.Arg1910=
XM_011545469.1:c.5729_5734delinsGGAAAA	XP_011543771.1:p.Arg1910=
XM_006724469.3:c.5705_5710delinsGGAAAA	XP_006724532.1:p.Arg1902=
XM_006724470.3:c.5729_5734delinsGGAAAA	XP_006724533.1:p.Arg1910=
XM_006724474.3:c.5729_5734delinsGGAAAA	XP_006724537.1:p.Arg1910=
XM_011545468.2:c.5729_5734delinsGGAAAA	XP_011543770.1:p.Arg1910=
XM_017029328.1:c.5729_5734delinsGGAAAA	XP_016884817.1:p.Arg1910=
XM_017029329.1:c.5729_5734delinsGGAAAA	XP_016884818.1:p.Arg1910=
XM_017029330.2:c.5729_5734delinsGGAAAA	XP_016884819.1:p.Arg1910=
NM_000109.4:c.5705_5710delinsGGAAAA	NP_000100.3:p.Arg1902=
NM_004006.3:c.5729_5734delinsGGAAAA MANE Select	NP_003997.2:p.Arg1910=
NM_004011.4:c.1706_1711delinsGGAAAA	NP_004002.3:p.Arg569=
NM_004012.4:c.1697_1702delinsGGAAAA	NP_004003.2:p.Arg566=