Canonical Allele Identifier: CA2567539777

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32464944_32464945insGT , CM000685.2:g.32464944_32464945insGT	GRCh38
NC_000023.10:g.32483061_32483062insGT , CM000685.1:g.32483061_32483062insGT	GRCh37
NC_000023.9:g.32392982_32392983insGT	NCBI36
NG_012232.1:g.879665_879666insAC , LRG_199:g.879665_879666insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682899.1:n.3370-246_3370-245insAC
ENST00000357033.9:c.3163-246_3163-245insAC MANE Select	ENSP00000354923.3:n.3163-246_3163-245insAC
ENST00000357033.8:c.3163-246_3163-245insAC	ENSP00000354923.3:n.3163-246_3163-245insAC
ENST00000378677.6:c.3151-246_3151-245insAC	ENSP00000367948.2:n.3151-246_3151-245insAC
ENST00000420596.5:c.94-99746_94-99745insAC	ENSP00000399897.1:n.94-99746_94-99745insAC
ENST00000448370.5:c.94-100235_94-100234insAC	ENSP00000388559.1:n.94-100235_94-100234insAC
ENST00000488902.5:n.336-247882_336-247881insAC
ENST00000619831.4:c.3151-246_3151-245insAC	ENSP00000479270.1:n.3151-246_3151-245insAC
ENST00000620040.4:c.3163-246_3163-245insAC	ENSP00000478150.1:n.3163-246_3163-245insAC
NM_000109.3:c.3139-246_3139-245insAC	NP_000100.2:n.3139-246_3139-245insAC
NM_004006.2:c.3163-246_3163-245insAC , LRG_199t1:c.3163-246_3163-245insAC	NP_003997.1:n.3163-246_3163-245insAC
NM_004009.3:c.3151-246_3151-245insAC	NP_004000.1:n.3151-246_3151-245insAC
NM_004010.3:c.2794-246_2794-245insAC	NP_004001.1:n.2794-246_2794-245insAC
XM_006724468.2:c.3163-246_3163-245insAC	XP_006724531.1:n.3163-246_3163-245insAC
XM_006724469.2:c.3139-246_3139-245insAC	XP_006724532.1:n.3139-246_3139-245insAC
XM_006724470.2:c.3163-246_3163-245insAC	XP_006724533.1:n.3163-246_3163-245insAC
XM_006724471.2:c.3163-246_3163-245insAC	XP_006724534.1:n.3163-246_3163-245insAC
XM_006724472.2:c.3034-246_3034-245insAC	XP_006724535.1:n.3034-246_3034-245insAC
XM_006724473.2:c.3163-246_3163-245insAC	XP_006724536.1:n.3163-246_3163-245insAC
XM_006724474.2:c.3163-246_3163-245insAC	XP_006724537.1:n.3163-246_3163-245insAC
XM_006724475.2:c.3163-246_3163-245insAC	XP_006724538.1:n.3163-246_3163-245insAC
XM_011545467.1:c.3163-246_3163-245insAC	XP_011543769.1:n.3163-246_3163-245insAC
XM_011545468.1:c.3163-246_3163-245insAC	XP_011543770.1:n.3163-246_3163-245insAC
XM_011545469.1:c.3163-246_3163-245insAC	XP_011543771.1:n.3163-246_3163-245insAC
XM_006724469.3:c.3139-246_3139-245insAC	XP_006724532.1:n.3139-246_3139-245insAC
XM_006724470.3:c.3163-246_3163-245insAC	XP_006724533.1:n.3163-246_3163-245insAC
XM_006724474.3:c.3163-246_3163-245insAC	XP_006724537.1:n.3163-246_3163-245insAC
XM_011545468.2:c.3163-246_3163-245insAC	XP_011543770.1:n.3163-246_3163-245insAC
XM_017029328.1:c.3163-246_3163-245insAC	XP_016884817.1:n.3163-246_3163-245insAC
XM_017029329.1:c.3163-246_3163-245insAC	XP_016884818.1:n.3163-246_3163-245insAC
XM_017029330.2:c.3163-246_3163-245insAC	XP_016884819.1:n.3163-246_3163-245insAC
NM_000109.4:c.3139-246_3139-245insAC	NP_000100.3:n.3139-246_3139-245insAC
NM_004006.3:c.3163-246_3163-245insAC MANE Select	NP_003997.2:n.3163-246_3163-245insAC