Canonical Allele Identifier: CA2423087269

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.33020112_33020117delinsAAAAGT , CM000685.2:g.33020112_33020117delinsAAAAGT	GRCh38
NC_000023.10:g.33038229_33038234delinsAAAAGT , CM000685.1:g.33038229_33038234delinsAAAAGT	GRCh37
NC_000023.9:g.32948150_32948155delinsAAAAGT	NCBI36
NG_012232.1:g.324493_324498delinsACTTTT , LRG_199:g.324493_324498delinsACTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000682071.1:c.-277+22_-277+27delinsACTTTT	ENSP00000508133.1:n.-277+22_-277+27delinsACTTTT
ENST00000682307.1:n.277+22_277+27delinsACTTTT
ENST00000682437.1:n.277+22_277+27delinsACTTTT
ENST00000682439.1:n.299_304delinsACTTTT
ENST00000682584.1:n.277+22_277+27delinsACTTTT
ENST00000682870.1:n.278+22_278+27delinsACTTTT
ENST00000682899.1:n.300+22_300+27delinsACTTTT
ENST00000682924.1:c.93+22_93+27delinsACTTTT	ENSP00000508187.1:n.93+22_93+27delinsACTTTT
ENST00000683309.1:n.277+22_277+27delinsACTTTT
ENST00000683658.1:n.438+22_438+27delinsACTTTT
ENST00000683985.1:n.300+22_300+27delinsACTTTT
ENST00000684056.1:n.277+22_277+27delinsACTTTT
ENST00000684165.1:n.300+22_300+27delinsACTTTT
ENST00000684237.1:c.93+22_93+27delinsACTTTT	ENSP00000507277.1:n.93+22_93+27delinsACTTTT
ENST00000684292.1:n.300+22_300+27delinsACTTTT
ENST00000684357.1:n.277+22_277+27delinsACTTTT
ENST00000684660.1:n.278+22_278+27delinsACTTTT
ENST00000288447.9:c.69+22_69+27delinsACTTTT	ENSP00000288447.4:n.69+22_69+27delinsACTTTT
ENST00000357033.9:c.93+22_93+27delinsACTTTT MANE Select	ENSP00000354923.3:n.93+22_93+27delinsACTTTT
ENST00000288447.8:c.69+22_69+27delinsACTTTT	ENSP00000288447.4:n.69+22_69+27delinsACTTTT
ENST00000357033.8:c.93+22_93+27delinsACTTTT	ENSP00000354923.3:n.93+22_93+27delinsACTTTT
ENST00000378677.6:c.81+22_81+27delinsACTTTT	ENSP00000367948.2:n.81+22_81+27delinsACTTTT
ENST00000420596.5:c.93+22_93+27delinsACTTTT	ENSP00000399897.1:n.93+22_93+27delinsACTTTT
ENST00000448370.5:c.93+22_93+27delinsACTTTT	ENSP00000388559.1:n.93+22_93+27delinsACTTTT
ENST00000472681.1:n.138+22_138+27delinsACTTTT
ENST00000488902.5:n.335+22_335+27delinsACTTTT
ENST00000619831.4:c.81+22_81+27delinsACTTTT	ENSP00000479270.1:n.81+22_81+27delinsACTTTT
ENST00000620040.4:c.93+22_93+27delinsACTTTT	ENSP00000478150.1:n.93+22_93+27delinsACTTTT
NM_000109.3:c.69+22_69+27delinsACTTTT	NP_000100.2:n.69+22_69+27delinsACTTTT
NM_004006.2:c.93+22_93+27delinsACTTTT , LRG_199t1:c.93+22_93+27delinsACTTTT	NP_003997.1:n.93+22_93+27delinsACTTTT
NM_004009.3:c.81+22_81+27delinsACTTTT	NP_004000.1:n.81+22_81+27delinsACTTTT
NM_004010.3:c.-277+22_-277+27delinsACTTTT	NP_004001.1:n.-277+22_-277+27delinsACTTTT
XM_006724468.2:c.93+22_93+27delinsACTTTT	XP_006724531.1:n.93+22_93+27delinsACTTTT
XM_006724469.2:c.69+22_69+27delinsACTTTT	XP_006724532.1:n.69+22_69+27delinsACTTTT
XM_006724470.2:c.93+22_93+27delinsACTTTT	XP_006724533.1:n.93+22_93+27delinsACTTTT
XM_006724471.2:c.93+22_93+27delinsACTTTT	XP_006724534.1:n.93+22_93+27delinsACTTTT
XM_006724472.2:c.93+22_93+27delinsACTTTT	XP_006724535.1:n.93+22_93+27delinsACTTTT
XM_006724473.2:c.93+22_93+27delinsACTTTT	XP_006724536.1:n.93+22_93+27delinsACTTTT
XM_006724474.2:c.93+22_93+27delinsACTTTT	XP_006724537.1:n.93+22_93+27delinsACTTTT
XM_006724475.2:c.93+22_93+27delinsACTTTT	XP_006724538.1:n.93+22_93+27delinsACTTTT
XM_011545467.1:c.93+22_93+27delinsACTTTT	XP_011543769.1:n.93+22_93+27delinsACTTTT
XM_011545468.1:c.93+22_93+27delinsACTTTT	XP_011543770.1:n.93+22_93+27delinsACTTTT
XM_011545469.1:c.93+22_93+27delinsACTTTT	XP_011543771.1:n.93+22_93+27delinsACTTTT
XM_006724469.3:c.69+22_69+27delinsACTTTT	XP_006724532.1:n.69+22_69+27delinsACTTTT
XM_006724470.3:c.93+22_93+27delinsACTTTT	XP_006724533.1:n.93+22_93+27delinsACTTTT
XM_006724474.3:c.93+22_93+27delinsACTTTT	XP_006724537.1:n.93+22_93+27delinsACTTTT
XM_011545468.2:c.93+22_93+27delinsACTTTT	XP_011543770.1:n.93+22_93+27delinsACTTTT
XM_017029328.1:c.93+22_93+27delinsACTTTT	XP_016884817.1:n.93+22_93+27delinsACTTTT
XM_017029329.1:c.93+22_93+27delinsACTTTT	XP_016884818.1:n.93+22_93+27delinsACTTTT
XM_017029330.2:c.93+22_93+27delinsACTTTT	XP_016884819.1:n.93+22_93+27delinsACTTTT
NM_000109.4:c.69+22_69+27delinsACTTTT	NP_000100.3:n.69+22_69+27delinsACTTTT
NM_004006.3:c.93+22_93+27delinsACTTTT MANE Select	NP_003997.2:n.93+22_93+27delinsACTTTT