Canonical Allele Identifier: CA2422829037

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32491171_32491174delinsTAGA , CM000685.2:g.32491171_32491174delinsTAGA	GRCh38
NC_000023.10:g.32509288_32509291delinsTAGA , CM000685.1:g.32509288_32509291delinsTAGA	GRCh37
NC_000023.9:g.32419209_32419212delinsTAGA	NCBI36
NG_012232.1:g.853436_853439delinsTCTA , LRG_199:g.853436_853439delinsTCTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000682899.1:n.2829+103_2829+106delinsTCTA
ENST00000683985.1:n.2829+103_2829+106delinsTCTA
ENST00000357033.9:c.2622+103_2622+106delinsTCTA MANE Select	ENSP00000354923.3:n.2622+103_2622+106delinsTCTA
ENST00000357033.8:c.2622+103_2622+106delinsTCTA	ENSP00000354923.3:n.2622+103_2622+106delinsTCTA
ENST00000378677.6:c.2610+103_2610+106delinsTCTA	ENSP00000367948.2:n.2610+103_2610+106delinsTCTA
ENST00000420596.5:c.94-125975_94-125972delinsTCTA	ENSP00000399897.1:n.94-125975_94-125972delinsTCTA
ENST00000448370.5:c.94-126464_94-126461delinsTCTA	ENSP00000388559.1:n.94-126464_94-126461delinsTCTA
ENST00000488902.5:n.336-274111_336-274108delinsTCTA
ENST00000619831.4:c.2610+103_2610+106delinsTCTA	ENSP00000479270.1:n.2610+103_2610+106delinsTCTA
ENST00000620040.4:c.2622+103_2622+106delinsTCTA	ENSP00000478150.1:n.2622+103_2622+106delinsTCTA
NM_000109.3:c.2598+103_2598+106delinsTCTA	NP_000100.2:n.2598+103_2598+106delinsTCTA
NM_004006.2:c.2622+103_2622+106delinsTCTA , LRG_199t1:c.2622+103_2622+106delinsTCTA	NP_003997.1:n.2622+103_2622+106delinsTCTA
NM_004009.3:c.2610+103_2610+106delinsTCTA	NP_004000.1:n.2610+103_2610+106delinsTCTA
NM_004010.3:c.2253+103_2253+106delinsTCTA	NP_004001.1:n.2253+103_2253+106delinsTCTA
XM_006724468.2:c.2622+103_2622+106delinsTCTA	XP_006724531.1:n.2622+103_2622+106delinsTCTA
XM_006724469.2:c.2598+103_2598+106delinsTCTA	XP_006724532.1:n.2598+103_2598+106delinsTCTA
XM_006724470.2:c.2622+103_2622+106delinsTCTA	XP_006724533.1:n.2622+103_2622+106delinsTCTA
XM_006724471.2:c.2622+103_2622+106delinsTCTA	XP_006724534.1:n.2622+103_2622+106delinsTCTA
XM_006724472.2:c.2493+103_2493+106delinsTCTA	XP_006724535.1:n.2493+103_2493+106delinsTCTA
XM_006724473.2:c.2622+103_2622+106delinsTCTA	XP_006724536.1:n.2622+103_2622+106delinsTCTA
XM_006724474.2:c.2622+103_2622+106delinsTCTA	XP_006724537.1:n.2622+103_2622+106delinsTCTA
XM_006724475.2:c.2622+103_2622+106delinsTCTA	XP_006724538.1:n.2622+103_2622+106delinsTCTA
XM_011545467.1:c.2622+103_2622+106delinsTCTA	XP_011543769.1:n.2622+103_2622+106delinsTCTA
XM_011545468.1:c.2622+103_2622+106delinsTCTA	XP_011543770.1:n.2622+103_2622+106delinsTCTA
XM_011545469.1:c.2622+103_2622+106delinsTCTA	XP_011543771.1:n.2622+103_2622+106delinsTCTA
XM_006724469.3:c.2598+103_2598+106delinsTCTA	XP_006724532.1:n.2598+103_2598+106delinsTCTA
XM_006724470.3:c.2622+103_2622+106delinsTCTA	XP_006724533.1:n.2622+103_2622+106delinsTCTA
XM_006724474.3:c.2622+103_2622+106delinsTCTA	XP_006724537.1:n.2622+103_2622+106delinsTCTA
XM_011545468.2:c.2622+103_2622+106delinsTCTA	XP_011543770.1:n.2622+103_2622+106delinsTCTA
XM_017029328.1:c.2622+103_2622+106delinsTCTA	XP_016884817.1:n.2622+103_2622+106delinsTCTA
XM_017029329.1:c.2622+103_2622+106delinsTCTA	XP_016884818.1:n.2622+103_2622+106delinsTCTA
XM_017029330.2:c.2622+103_2622+106delinsTCTA	XP_016884819.1:n.2622+103_2622+106delinsTCTA
NM_000109.4:c.2598+103_2598+106delinsTCTA	NP_000100.3:n.2598+103_2598+106delinsTCTA
NM_004006.3:c.2622+103_2622+106delinsTCTA MANE Select	NP_003997.2:n.2622+103_2622+106delinsTCTA