Canonical Allele Identifier: CA2422548663

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31774136T= , CM000685.2:g.31774136T=	GRCh38
NC_000023.10:g.31792253T= , CM000685.1:g.31792253T=	GRCh37
NC_000023.9:g.31702174T=	NCBI36
NG_012232.1:g.1570474A= , LRG_199:g.1570474A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.2212A=	ENSP00000350765.3:p.Ile738=
ENST00000682238.1:c.-15A=	ENSP00000508124.1:n.-15A=
ENST00000683117.1:n.1027A=
ENST00000683450.1:n.949A=
ENST00000683851.1:n.1027A=
ENST00000683957.1:n.858A=
ENST00000684130.1:c.-15A=	ENSP00000508037.1:n.-15A=
ENST00000357033.9:c.7366A= MANE Select	ENSP00000354923.3:p.Ile2456=
ENST00000619831.5:c.3334A=	ENSP00000479270.2:p.Ile1112=
ENST00000620040.5:c.-15A=	ENSP00000478150.2:n.-15A=
ENST00000680961.1:c.-15A=	ENSP00000506386.1:n.-15A=
ENST00000681646.1:n.1027A=
ENST00000681839.1:c.355A=	ENSP00000505228.1:p.Ile119=
ENST00000357033.8:c.7366A=	ENSP00000354923.3:p.Ile2456=
ENST00000358062.6:c.454A=	ENSP00000350765.2:p.Ile152=
ENST00000359836.5:c.-15A=	ENSP00000352894.1:n.-15A=
ENST00000378677.6:c.7354A=	ENSP00000367948.2:p.Ile2452=
ENST00000378707.7:c.-15A=	ENSP00000367979.3:n.-15A=
ENST00000471779.1:c.123A=	ENSP00000417075.1:n.123A=
ENST00000474231.5:c.-15A=	ENSP00000417123.1:n.-15A=
ENST00000541735.5:c.-15A=	ENSP00000444119.1:n.-15A=
ENST00000619831.4:c.7351A=	ENSP00000479270.1:p.Ile2451=
ENST00000620040.4:c.7363A=	ENSP00000478150.1:p.Ile2455=
NM_000109.3:c.7342A=	NP_000100.2:p.Ile2448=
NM_004006.2:c.7366A= , LRG_199t1:c.7366A=	NP_003997.1:p.Ile2456=
NM_004009.3:c.7354A=	NP_004000.1:p.Ile2452=
NM_004010.3:c.6997A=	NP_004001.1:p.Ile2333=
NM_004011.3:c.3343A=	NP_004002.2:p.Ile1115=
NM_004012.3:c.3334A=	NP_004003.1:p.Ile1112=
NM_004013.2:c.-15A=	NP_004004.1:n.-15A=
NM_004020.3:c.-15A=	NP_004011.2:n.-15A=
NM_004021.2:c.-15A=	NP_004012.1:n.-15A=
NM_004022.2:c.-15A=	NP_004013.1:n.-15A=
NM_004023.2:c.-15A=	NP_004014.1:n.-15A=
XM_006724468.2:c.7366A=	XP_006724531.1:p.Ile2456=
XM_006724469.2:c.7342A=	XP_006724532.1:p.Ile2448=
XM_006724470.2:c.7366A=	XP_006724533.1:p.Ile2456=
XM_006724471.2:c.7366A=	XP_006724534.1:p.Ile2456=
XM_006724472.2:c.7237A=	XP_006724535.1:p.Ile2413=
XM_006724473.2:c.7228A=	XP_006724536.1:p.Ile2410=
XM_006724474.2:c.7366A=	XP_006724537.1:p.Ile2456=
XM_006724475.2:c.7366A=	XP_006724538.1:p.Ile2456=
XM_011545467.1:c.7243A=	XP_011543769.1:p.Ile2415=
XM_011545468.1:c.7366A=	XP_011543770.1:p.Ile2456=
XM_006724469.3:c.7342A=	XP_006724532.1:p.Ile2448=
XM_006724470.3:c.7366A=	XP_006724533.1:p.Ile2456=
XM_006724474.3:c.7366A=	XP_006724537.1:p.Ile2456=
XM_011545468.2:c.7366A=	XP_011543770.1:p.Ile2456=
XM_017029328.1:c.7366A=	XP_016884817.1:p.Ile2456=
XM_017029331.1:c.1540A=	XP_016884820.1:p.Ile514=
NM_000109.4:c.7342A=	NP_000100.3:p.Ile2448=
NM_004006.3:c.7366A= MANE Select	NP_003997.2:p.Ile2456=
NM_004011.4:c.3343A=	NP_004002.3:p.Ile1115=
NM_004012.4:c.3334A=	NP_004003.2:p.Ile1112=
NM_004021.3:c.-15A=	NP_004012.2:n.-15A=
NM_004023.3:c.-15A=	NP_004014.2:n.-15A=
NM_004013.3:c.-15A=	NP_004004.2:n.-15A=
NM_004020.4:c.-15A=	NP_004011.3:n.-15A=
NM_004022.3:c.-15A=	NP_004013.2:n.-15A=