Canonical Allele Identifier: CA2422434075

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31444606G= , CM000685.2:g.31444606G=	GRCh38
NC_000023.10:g.31462723G= , CM000685.1:g.31462723G=	GRCh37
NC_000023.9:g.31372644G=	NCBI36
NG_012232.1:g.1900004C= , LRG_199:g.1900004C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.3805C=	ENSP00000350765.3:p.Pro1269=
ENST00000682238.1:c.1579C=	ENSP00000508124.1:p.Pro527=
ENST00000683450.1:n.2424C=
ENST00000683957.1:n.2451C=
ENST00000684130.1:c.1579C=	ENSP00000508037.1:p.Pro527=
ENST00000343523.7:c.814C=	ENSP00000340057.4:p.Pro272=
ENST00000357033.9:c.8959C= MANE Select	ENSP00000354923.3:p.Pro2987=
ENST00000619831.5:c.4927C=	ENSP00000479270.2:p.Pro1643=
ENST00000620040.5:c.1579C=	ENSP00000478150.2:p.Pro527=
ENST00000680961.1:c.1579C=	ENSP00000506386.1:p.Pro527=
ENST00000681646.1:n.2620C=
ENST00000343523.6:c.772C=	ENSP00000340057.3:p.Pro258=
ENST00000357033.8:c.8959C=	ENSP00000354923.3:p.Pro2987=
ENST00000358062.6:c.2047C=	ENSP00000350765.2:p.Pro683=
ENST00000359836.5:c.1579C=	ENSP00000352894.1:p.Pro527=
ENST00000378677.6:c.8947C=	ENSP00000367948.2:p.Pro2983=
ENST00000378707.7:c.1579C=	ENSP00000367979.3:p.Pro527=
ENST00000474231.5:c.1579C=	ENSP00000417123.1:p.Pro527=
ENST00000541735.5:c.1579C=	ENSP00000444119.1:p.Pro527=
ENST00000619831.4:c.8944C=	ENSP00000479270.1:p.Pro2982=
ENST00000620040.4:c.8956C=	ENSP00000478150.1:p.Pro2986=
NM_000109.3:c.8935C=	NP_000100.2:p.Pro2979=
NM_004006.2:c.8959C= , LRG_199t1:c.8959C=	NP_003997.1:p.Pro2987=
NM_004009.3:c.8947C=	NP_004000.1:p.Pro2983=
NM_004010.3:c.8590C=	NP_004001.1:p.Pro2864=
NM_004011.3:c.4936C=	NP_004002.2:p.Pro1646=
NM_004012.3:c.4927C=	NP_004003.1:p.Pro1643=
NM_004013.2:c.1579C=	NP_004004.1:p.Pro527=
NM_004014.2:c.772C=	NP_004005.1:p.Pro258=
NM_004020.3:c.1579C=	NP_004011.2:p.Pro527=
NM_004021.2:c.1579C=	NP_004012.1:p.Pro527=
NM_004022.2:c.1579C=	NP_004013.1:p.Pro527=
NM_004023.2:c.1579C=	NP_004014.1:p.Pro527=
XM_006724468.2:c.8959C=	XP_006724531.1:p.Pro2987=
XM_006724469.2:c.8935C=	XP_006724532.1:p.Pro2979=
XM_006724470.2:c.8959C=	XP_006724533.1:p.Pro2987=
XM_006724471.2:c.8959C=	XP_006724534.1:p.Pro2987=
XM_006724472.2:c.8830C=	XP_006724535.1:p.Pro2944=
XM_006724473.2:c.8821C=	XP_006724536.1:p.Pro2941=
XM_006724474.2:c.8959C=	XP_006724537.1:p.Pro2987=
XM_006724475.2:c.8959C=	XP_006724538.1:p.Pro2987=
XM_011545467.1:c.8836C=	XP_011543769.1:p.Pro2946=
XM_011545468.1:c.8959C=	XP_011543770.1:p.Pro2987=
XM_006724469.3:c.8935C=	XP_006724532.1:p.Pro2979=
XM_006724470.3:c.8959C=	XP_006724533.1:p.Pro2987=
XM_006724474.3:c.8959C=	XP_006724537.1:p.Pro2987=
XM_011545468.2:c.8959C=	XP_011543770.1:p.Pro2987=
XM_017029328.1:c.8959C=	XP_016884817.1:p.Pro2987=
XM_017029331.1:c.3133C=	XP_016884820.1:p.Pro1045=
NM_000109.4:c.8935C=	NP_000100.3:p.Pro2979=
NM_004006.3:c.8959C= MANE Select	NP_003997.2:p.Pro2987=
NM_004011.4:c.4936C=	NP_004002.3:p.Pro1646=
NM_004012.4:c.4927C=	NP_004003.2:p.Pro1643=
NM_004021.3:c.1579C=	NP_004012.2:p.Pro527=
NM_004023.3:c.1579C=	NP_004014.2:p.Pro527=
NM_004013.3:c.1579C=	NP_004004.2:p.Pro527=
NM_004014.3:c.772C=	NP_004005.2:p.Pro258=
NM_004020.4:c.1579C=	NP_004011.3:p.Pro527=
NM_004022.3:c.1579C=	NP_004013.2:p.Pro527=