Canonical Allele Identifier: CA2820325829

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32464703_32464704insT , CM000685.2:g.32464703_32464704insT	GRCh38
NC_000023.10:g.32482820_32482821insT , CM000685.1:g.32482820_32482821insT	GRCh37
NC_000023.9:g.32392741_32392742insT	NCBI36
NG_012232.1:g.879906_879907insA , LRG_199:g.879906_879907insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682899.1:n.3370-5_3370-4insA
ENST00000357033.9:c.3163-5_3163-4insA MANE Select	ENSP00000354923.3:n.3163-5_3163-4insA
ENST00000357033.8:c.3163-5_3163-4insA	ENSP00000354923.3:n.3163-5_3163-4insA
ENST00000378677.6:c.3151-5_3151-4insA	ENSP00000367948.2:n.3151-5_3151-4insA
ENST00000420596.5:c.94-99505_94-99504insA	ENSP00000399897.1:n.94-99505_94-99504insA
ENST00000448370.5:c.94-99994_94-99993insA	ENSP00000388559.1:n.94-99994_94-99993insA
ENST00000488902.5:n.336-247641_336-247640insA
ENST00000619831.4:c.3151-5_3151-4insA	ENSP00000479270.1:n.3151-5_3151-4insA
ENST00000620040.4:c.3163-5_3163-4insA	ENSP00000478150.1:n.3163-5_3163-4insA
NM_000109.3:c.3139-5_3139-4insA	NP_000100.2:n.3139-5_3139-4insA
NM_004006.2:c.3163-5_3163-4insA , LRG_199t1:c.3163-5_3163-4insA	NP_003997.1:n.3163-5_3163-4insA
NM_004009.3:c.3151-5_3151-4insA	NP_004000.1:n.3151-5_3151-4insA
NM_004010.3:c.2794-5_2794-4insA	NP_004001.1:n.2794-5_2794-4insA
XM_006724468.2:c.3163-5_3163-4insA	XP_006724531.1:n.3163-5_3163-4insA
XM_006724469.2:c.3139-5_3139-4insA	XP_006724532.1:n.3139-5_3139-4insA
XM_006724470.2:c.3163-5_3163-4insA	XP_006724533.1:n.3163-5_3163-4insA
XM_006724471.2:c.3163-5_3163-4insA	XP_006724534.1:n.3163-5_3163-4insA
XM_006724472.2:c.3034-5_3034-4insA	XP_006724535.1:n.3034-5_3034-4insA
XM_006724473.2:c.3163-5_3163-4insA	XP_006724536.1:n.3163-5_3163-4insA
XM_006724474.2:c.3163-5_3163-4insA	XP_006724537.1:n.3163-5_3163-4insA
XM_006724475.2:c.3163-5_3163-4insA	XP_006724538.1:n.3163-5_3163-4insA
XM_011545467.1:c.3163-5_3163-4insA	XP_011543769.1:n.3163-5_3163-4insA
XM_011545468.1:c.3163-5_3163-4insA	XP_011543770.1:n.3163-5_3163-4insA
XM_011545469.1:c.3163-5_3163-4insA	XP_011543771.1:n.3163-5_3163-4insA
XM_006724469.3:c.3139-5_3139-4insA	XP_006724532.1:n.3139-5_3139-4insA
XM_006724470.3:c.3163-5_3163-4insA	XP_006724533.1:n.3163-5_3163-4insA
XM_006724474.3:c.3163-5_3163-4insA	XP_006724537.1:n.3163-5_3163-4insA
XM_011545468.2:c.3163-5_3163-4insA	XP_011543770.1:n.3163-5_3163-4insA
XM_017029328.1:c.3163-5_3163-4insA	XP_016884817.1:n.3163-5_3163-4insA
XM_017029329.1:c.3163-5_3163-4insA	XP_016884818.1:n.3163-5_3163-4insA
XM_017029330.2:c.3163-5_3163-4insA	XP_016884819.1:n.3163-5_3163-4insA
NM_000109.4:c.3139-5_3139-4insA	NP_000100.3:n.3139-5_3139-4insA
NM_004006.3:c.3163-5_3163-4insA MANE Select	NP_003997.2:n.3163-5_3163-4insA