Canonical Allele Identifier: CA2422811279

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32454858_32454859delinsAC , CM000685.2:g.32454858_32454859delinsAC	GRCh38
NC_000023.10:g.32472975_32472976delinsAC , CM000685.1:g.32472975_32472976delinsAC	GRCh37
NC_000023.9:g.32382896_32382897delinsAC	NCBI36
NG_012232.1:g.889751_889752delinsGT , LRG_199:g.889751_889752delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682899.1:n.3640-27_3640-26delinsGT
ENST00000357033.9:c.3433-27_3433-26delinsGT MANE Select	ENSP00000354923.3:n.3433-27_3433-26delinsGT
ENST00000357033.8:c.3433-27_3433-26delinsGT	ENSP00000354923.3:n.3433-27_3433-26delinsGT
ENST00000378677.6:c.3421-27_3421-26delinsGT	ENSP00000367948.2:n.3421-27_3421-26delinsGT
ENST00000420596.5:c.94-89660_94-89659delinsGT	ENSP00000399897.1:n.94-89660_94-89659delinsGT
ENST00000448370.5:c.94-90149_94-90148delinsGT	ENSP00000388559.1:n.94-90149_94-90148delinsGT
ENST00000488902.5:n.336-237796_336-237795delinsGT
ENST00000619831.4:c.3421-27_3421-26delinsGT	ENSP00000479270.1:n.3421-27_3421-26delinsGT
ENST00000620040.4:c.3433-27_3433-26delinsGT	ENSP00000478150.1:n.3433-27_3433-26delinsGT
NM_000109.3:c.3409-27_3409-26delinsGT	NP_000100.2:n.3409-27_3409-26delinsGT
NM_004006.2:c.3433-27_3433-26delinsGT , LRG_199t1:c.3433-27_3433-26delinsGT	NP_003997.1:n.3433-27_3433-26delinsGT
NM_004009.3:c.3421-27_3421-26delinsGT	NP_004000.1:n.3421-27_3421-26delinsGT
NM_004010.3:c.3064-27_3064-26delinsGT	NP_004001.1:n.3064-27_3064-26delinsGT
XM_006724468.2:c.3433-27_3433-26delinsGT	XP_006724531.1:n.3433-27_3433-26delinsGT
XM_006724469.2:c.3409-27_3409-26delinsGT	XP_006724532.1:n.3409-27_3409-26delinsGT
XM_006724470.2:c.3433-27_3433-26delinsGT	XP_006724533.1:n.3433-27_3433-26delinsGT
XM_006724471.2:c.3433-27_3433-26delinsGT	XP_006724534.1:n.3433-27_3433-26delinsGT
XM_006724472.2:c.3304-27_3304-26delinsGT	XP_006724535.1:n.3304-27_3304-26delinsGT
XM_006724473.2:c.3433-27_3433-26delinsGT	XP_006724536.1:n.3433-27_3433-26delinsGT
XM_006724474.2:c.3433-27_3433-26delinsGT	XP_006724537.1:n.3433-27_3433-26delinsGT
XM_006724475.2:c.3433-27_3433-26delinsGT	XP_006724538.1:n.3433-27_3433-26delinsGT
XM_011545467.1:c.3433-27_3433-26delinsGT	XP_011543769.1:n.3433-27_3433-26delinsGT
XM_011545468.1:c.3433-27_3433-26delinsGT	XP_011543770.1:n.3433-27_3433-26delinsGT
XM_011545469.1:c.3433-27_3433-26delinsGT	XP_011543771.1:n.3433-27_3433-26delinsGT
XM_006724469.3:c.3409-27_3409-26delinsGT	XP_006724532.1:n.3409-27_3409-26delinsGT
XM_006724470.3:c.3433-27_3433-26delinsGT	XP_006724533.1:n.3433-27_3433-26delinsGT
XM_006724474.3:c.3433-27_3433-26delinsGT	XP_006724537.1:n.3433-27_3433-26delinsGT
XM_011545468.2:c.3433-27_3433-26delinsGT	XP_011543770.1:n.3433-27_3433-26delinsGT
XM_017029328.1:c.3433-27_3433-26delinsGT	XP_016884817.1:n.3433-27_3433-26delinsGT
XM_017029329.1:c.3433-27_3433-26delinsGT	XP_016884818.1:n.3433-27_3433-26delinsGT
XM_017029330.2:c.3433-27_3433-26delinsGT	XP_016884819.1:n.3433-27_3433-26delinsGT
NM_000109.4:c.3409-27_3409-26delinsGT	NP_000100.3:n.3409-27_3409-26delinsGT
NM_004006.3:c.3433-27_3433-26delinsGT MANE Select	NP_003997.2:n.3433-27_3433-26delinsGT