Canonical Allele Identifier: CA2695234101

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32365023_32365024dup , CM000685.2:g.32365023_32365024dup	GRCh38
NC_000023.10:g.32383140_32383141dup , CM000685.1:g.32383140_32383141dup	GRCh37
NC_000023.9:g.32293061_32293062dup	NCBI36
NG_012232.1:g.979587_979588dup , LRG_199:g.979587_979588dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357033.9:c.5022_5023dup MANE Select	ENSP00000354923.3:p.Leu1675CysfsTer?
ENST00000619831.5:c.990_991dup	ENSP00000479270.2:p.Leu331CysfsTer?
ENST00000357033.8:c.5022_5023dup	ENSP00000354923.3:p.Leu1675CysfsTer?
ENST00000378677.6:c.5010_5011dup	ENSP00000367948.2:p.Leu1671CysfsTer?
ENST00000420596.5:c.270_271dup	ENSP00000399897.1:p.Leu91CysfsTer?
ENST00000448370.5:c.94-313_94-312dup	ENSP00000388559.1:n.94-313_94-312dup
ENST00000488902.5:n.336-147960_336-147959dup
ENST00000619831.4:c.5010_5011dup	ENSP00000479270.1:p.Leu1671CysfsTer?
ENST00000620040.4:c.5022_5023dup	ENSP00000478150.1:p.Leu1675CysfsTer?
NM_000109.3:c.4998_4999dup	NP_000100.2:p.Leu1667CysfsTer?
NM_004006.2:c.5022_5023dup , LRG_199t1:c.5022_5023dup	NP_003997.1:p.Leu1675CysfsTer?
NM_004009.3:c.5010_5011dup	NP_004000.1:p.Leu1671CysfsTer?
NM_004010.3:c.4653_4654dup	NP_004001.1:p.Leu1552CysfsTer?
NM_004011.3:c.999_1000dup	NP_004002.2:p.Leu334CysfsTer?
NM_004012.3:c.990_991dup	NP_004003.1:p.Leu331CysfsTer?
XM_006724468.2:c.5022_5023dup	XP_006724531.1:p.Leu1675CysfsTer?
XM_006724469.2:c.4998_4999dup	XP_006724532.1:p.Leu1667CysfsTer?
XM_006724470.2:c.5022_5023dup	XP_006724533.1:p.Leu1675CysfsTer?
XM_006724471.2:c.5022_5023dup	XP_006724534.1:p.Leu1675CysfsTer?
XM_006724472.2:c.4893_4894dup	XP_006724535.1:p.Leu1632CysfsTer?
XM_006724473.2:c.5022_5023dup	XP_006724536.1:p.Leu1675CysfsTer?
XM_006724474.2:c.5022_5023dup	XP_006724537.1:p.Leu1675CysfsTer?
XM_006724475.2:c.5022_5023dup	XP_006724538.1:p.Leu1675CysfsTer?
XM_011545467.1:c.5022_5023dup	XP_011543769.1:p.Leu1675CysfsTer?
XM_011545468.1:c.5022_5023dup	XP_011543770.1:p.Leu1675CysfsTer?
XM_011545469.1:c.5022_5023dup	XP_011543771.1:p.Leu1675CysfsTer?
XM_006724469.3:c.4998_4999dup	XP_006724532.1:p.Leu1667CysfsTer?
XM_006724470.3:c.5022_5023dup	XP_006724533.1:p.Leu1675CysfsTer?
XM_006724474.3:c.5022_5023dup	XP_006724537.1:p.Leu1675CysfsTer?
XM_011545468.2:c.5022_5023dup	XP_011543770.1:p.Leu1675CysfsTer?
XM_017029328.1:c.5022_5023dup	XP_016884817.1:p.Leu1675CysfsTer?
XM_017029329.1:c.5022_5023dup	XP_016884818.1:p.Leu1675CysfsTer?
XM_017029330.2:c.5022_5023dup	XP_016884819.1:p.Leu1675CysfsTer?
NM_000109.4:c.4998_4999dup	NP_000100.3:p.Leu1667CysfsTer?
NM_004006.3:c.5022_5023dup MANE Select	NP_003997.2:p.Leu1675CysfsTer?
NM_004011.4:c.999_1000dup	NP_004002.3:p.Leu334CysfsTer?
NM_004012.4:c.990_991dup	NP_004003.2:p.Leu331CysfsTer?