Canonical Allele Identifier: CA2422745219

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32310181_32310185delinsATGAG , CM000685.2:g.32310181_32310185delinsATGAG	GRCh38
NC_000023.10:g.32328298_32328302delinsATGAG , CM000685.1:g.32328298_32328302delinsATGAG	GRCh37
NC_000023.9:g.32238219_32238223delinsATGAG	NCBI36
NG_012232.1:g.1034425_1034429delinsCTCAT , LRG_199:g.1034425_1034429delinsCTCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.860_864delinsCTCAT	ENSP00000350765.3:p.Thr287=
ENST00000357033.9:c.6014_6018delinsCTCAT MANE Select	ENSP00000354923.3:p.Thr2005=
ENST00000619831.5:c.1982_1986delinsCTCAT	ENSP00000479270.2:p.Thr661=
ENST00000357033.8:c.6014_6018delinsCTCAT	ENSP00000354923.3:p.Thr2005=
ENST00000378677.6:c.6002_6006delinsCTCAT	ENSP00000367948.2:p.Thr2001=
ENST00000488902.5:n.336-93122_336-93118delinsCTCAT
ENST00000619831.4:c.6002_6006delinsCTCAT	ENSP00000479270.1:p.Thr2001=
ENST00000620040.4:c.6014_6018delinsCTCAT	ENSP00000478150.1:p.Thr2005=
NM_000109.3:c.5990_5994delinsCTCAT	NP_000100.2:p.Thr1997=
NM_004006.2:c.6014_6018delinsCTCAT , LRG_199t1:c.6014_6018delinsCTCAT	NP_003997.1:p.Thr2005=
NM_004009.3:c.6002_6006delinsCTCAT	NP_004000.1:p.Thr2001=
NM_004010.3:c.5645_5649delinsCTCAT	NP_004001.1:p.Thr1882=
NM_004011.3:c.1991_1995delinsCTCAT	NP_004002.2:p.Thr664=
NM_004012.3:c.1982_1986delinsCTCAT	NP_004003.1:p.Thr661=
XM_006724468.2:c.6014_6018delinsCTCAT	XP_006724531.1:p.Thr2005=
XM_006724469.2:c.5990_5994delinsCTCAT	XP_006724532.1:p.Thr1997=
XM_006724470.2:c.6014_6018delinsCTCAT	XP_006724533.1:p.Thr2005=
XM_006724471.2:c.6014_6018delinsCTCAT	XP_006724534.1:p.Thr2005=
XM_006724472.2:c.5885_5889delinsCTCAT	XP_006724535.1:p.Thr1962=
XM_006724473.2:c.5876_5880delinsCTCAT	XP_006724536.1:p.Thr1959=
XM_006724474.2:c.6014_6018delinsCTCAT	XP_006724537.1:p.Thr2005=
XM_006724475.2:c.6014_6018delinsCTCAT	XP_006724538.1:p.Thr2005=
XM_011545467.1:c.5891_5895delinsCTCAT	XP_011543769.1:p.Thr1964=
XM_011545468.1:c.6014_6018delinsCTCAT	XP_011543770.1:p.Thr2005=
XM_006724469.3:c.5990_5994delinsCTCAT	XP_006724532.1:p.Thr1997=
XM_006724470.3:c.6014_6018delinsCTCAT	XP_006724533.1:p.Thr2005=
XM_006724474.3:c.6014_6018delinsCTCAT	XP_006724537.1:p.Thr2005=
XM_011545468.2:c.6014_6018delinsCTCAT	XP_011543770.1:p.Thr2005=
XM_017029328.1:c.6014_6018delinsCTCAT	XP_016884817.1:p.Thr2005=
XM_017029329.1:c.6014_6018delinsCTCAT	XP_016884818.1:p.Thr2005=
XM_017029330.2:c.6014_6018delinsCTCAT	XP_016884819.1:p.Thr2005=
XM_017029331.1:c.188_192delinsCTCAT	XP_016884820.1:p.Thr63=
NM_000109.4:c.5990_5994delinsCTCAT	NP_000100.3:p.Thr1997=
NM_004006.3:c.6014_6018delinsCTCAT MANE Select	NP_003997.2:p.Thr2005=
NM_004011.4:c.1991_1995delinsCTCAT	NP_004002.3:p.Thr664=
NM_004012.4:c.1982_1986delinsCTCAT	NP_004003.2:p.Thr661=