Canonical Allele Identifier: CA2422995550

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32816474_32816476delinsCTA , CM000685.2:g.32816474_32816476delinsCTA	GRCh38
NC_000023.10:g.32834591_32834593delinsCTA , CM000685.1:g.32834591_32834593delinsCTA	GRCh37
NC_000023.9:g.32744512_32744514delinsCTA	NCBI36
NG_012232.1:g.528134_528136delinsTAG , LRG_199:g.528134_528136delinsTAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000682071.1:c.153_155delinsTAG	ENSP00000508133.1:p.His51=
ENST00000682437.1:n.846_848delinsTAG
ENST00000682870.1:n.707_709delinsTAG
ENST00000682899.1:n.729_731delinsTAG
ENST00000682924.1:c.522_524delinsTAG	ENSP00000508187.1:p.His174=
ENST00000683309.1:n.706_708delinsTAG
ENST00000683658.1:n.867_869delinsTAG
ENST00000683985.1:n.729_731delinsTAG
ENST00000684056.1:n.706_708delinsTAG
ENST00000684165.1:n.729_731delinsTAG
ENST00000684237.1:c.522_524delinsTAG	ENSP00000507277.1:p.His174=
ENST00000684292.1:n.729_731delinsTAG
ENST00000684660.1:n.707_709delinsTAG
ENST00000288447.9:c.498_500delinsTAG	ENSP00000288447.4:p.His166=
ENST00000357033.9:c.522_524delinsTAG MANE Select	ENSP00000354923.3:p.His174=
ENST00000288447.8:c.498_500delinsTAG	ENSP00000288447.4:p.His166=
ENST00000357033.8:c.522_524delinsTAG	ENSP00000354923.3:p.His174=
ENST00000378677.6:c.510_512delinsTAG	ENSP00000367948.2:p.His170=
ENST00000420596.5:c.93+203663_93+203665delinsTAG	ENSP00000399897.1:n.93+203663_93+203665delinsTAG
ENST00000447523.1:c.246+6819_246+6821delinsTAG	ENSP00000395904.1:n.246+6819_246+6821delinsTAG
ENST00000448370.5:c.93+203663_93+203665delinsTAG	ENSP00000388559.1:n.93+203663_93+203665delinsTAG
ENST00000480751.1:n.78_80delinsTAG
ENST00000488902.5:n.335+203663_335+203665delinsTAG
ENST00000619831.4:c.510_512delinsTAG	ENSP00000479270.1:p.His170=
ENST00000620040.4:c.522_524delinsTAG	ENSP00000478150.1:p.His174=
NM_000109.3:c.498_500delinsTAG	NP_000100.2:p.His166=
NM_004006.2:c.522_524delinsTAG , LRG_199t1:c.522_524delinsTAG	NP_003997.1:p.His174=
NM_004009.3:c.510_512delinsTAG	NP_004000.1:p.His170=
NM_004010.3:c.153_155delinsTAG	NP_004001.1:p.His51=
XM_006724468.2:c.522_524delinsTAG	XP_006724531.1:p.His174=
XM_006724469.2:c.498_500delinsTAG	XP_006724532.1:p.His166=
XM_006724470.2:c.522_524delinsTAG	XP_006724533.1:p.His174=
XM_006724471.2:c.522_524delinsTAG	XP_006724534.1:p.His174=
XM_006724472.2:c.522_524delinsTAG	XP_006724535.1:p.His174=
XM_006724473.2:c.522_524delinsTAG	XP_006724536.1:p.His174=
XM_006724474.2:c.522_524delinsTAG	XP_006724537.1:p.His174=
XM_006724475.2:c.522_524delinsTAG	XP_006724538.1:p.His174=
XM_011545467.1:c.522_524delinsTAG	XP_011543769.1:p.His174=
XM_011545468.1:c.522_524delinsTAG	XP_011543770.1:p.His174=
XM_011545469.1:c.522_524delinsTAG	XP_011543771.1:p.His174=
XM_006724469.3:c.498_500delinsTAG	XP_006724532.1:p.His166=
XM_006724470.3:c.522_524delinsTAG	XP_006724533.1:p.His174=
XM_006724474.3:c.522_524delinsTAG	XP_006724537.1:p.His174=
XM_011545468.2:c.522_524delinsTAG	XP_011543770.1:p.His174=
XM_017029328.1:c.522_524delinsTAG	XP_016884817.1:p.His174=
XM_017029329.1:c.522_524delinsTAG	XP_016884818.1:p.His174=
XM_017029330.2:c.522_524delinsTAG	XP_016884819.1:p.His174=
NM_000109.4:c.498_500delinsTAG	NP_000100.3:p.His166=
NM_004006.3:c.522_524delinsTAG MANE Select	NP_003997.2:p.His174=