Canonical Allele Identifier: CA2697552971

Gene: DMD

Linked Data

• ClinVar Variation Id: 2703317
• ClinVar RCV Id: RCV003512867

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32454666_32454670del , CM000685.2:g.32454666_32454670del	GRCh38
NC_000023.10:g.32472783_32472787del , CM000685.1:g.32472783_32472787del	GRCh37
NC_000023.9:g.32382704_32382708del	NCBI36
NG_012232.1:g.889942_889946del , LRG_199:g.889942_889946del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682899.1:n.3804_3808del
ENST00000357033.9:c.3597_3601del MANE Select	ENSP00000354923.3:p.Met1200GlufsTer3
ENST00000357033.8:c.3597_3601del	ENSP00000354923.3:p.Met1200GlufsTer3
ENST00000378677.6:c.3585_3589del	ENSP00000367948.2:p.Met1196GlufsTer3
ENST00000420596.5:c.94-89469_94-89465del	ENSP00000399897.1:n.94-89469_94-89465del
ENST00000448370.5:c.94-89958_94-89954del	ENSP00000388559.1:n.94-89958_94-89954del
ENST00000488902.5:n.336-237605_336-237601del
ENST00000619831.4:c.3585_3589del	ENSP00000479270.1:p.Met1196GlufsTer3
ENST00000620040.4:c.3597_3601del	ENSP00000478150.1:p.Met1200GlufsTer3
NM_000109.3:c.3573_3577del	NP_000100.2:p.Met1192GlufsTer3
NM_004006.2:c.3597_3601del , LRG_199t1:c.3597_3601del	NP_003997.1:p.Met1200GlufsTer3
NM_004009.3:c.3585_3589del	NP_004000.1:p.Met1196GlufsTer3
NM_004010.3:c.3228_3232del	NP_004001.1:p.Met1077GlufsTer3
XM_006724468.2:c.3597_3601del	XP_006724531.1:p.Met1200GlufsTer3
XM_006724469.2:c.3573_3577del	XP_006724532.1:p.Met1192GlufsTer3
XM_006724470.2:c.3597_3601del	XP_006724533.1:p.Met1200GlufsTer3
XM_006724471.2:c.3597_3601del	XP_006724534.1:p.Met1200GlufsTer3
XM_006724472.2:c.3468_3472del	XP_006724535.1:p.Met1157GlufsTer3
XM_006724473.2:c.3597_3601del	XP_006724536.1:p.Met1200GlufsTer3
XM_006724474.2:c.3597_3601del	XP_006724537.1:p.Met1200GlufsTer3
XM_006724475.2:c.3597_3601del	XP_006724538.1:p.Met1200GlufsTer3
XM_011545467.1:c.3597_3601del	XP_011543769.1:p.Met1200GlufsTer3
XM_011545468.1:c.3597_3601del	XP_011543770.1:p.Met1200GlufsTer3
XM_011545469.1:c.3597_3601del	XP_011543771.1:p.Met1200GlufsTer3
XM_006724469.3:c.3573_3577del	XP_006724532.1:p.Met1192GlufsTer3
XM_006724470.3:c.3597_3601del	XP_006724533.1:p.Met1200GlufsTer3
XM_006724474.3:c.3597_3601del	XP_006724537.1:p.Met1200GlufsTer3
XM_011545468.2:c.3597_3601del	XP_011543770.1:p.Met1200GlufsTer3
XM_017029328.1:c.3597_3601del	XP_016884817.1:p.Met1200GlufsTer3
XM_017029329.1:c.3597_3601del	XP_016884818.1:p.Met1200GlufsTer3
XM_017029330.2:c.3597_3601del	XP_016884819.1:p.Met1200GlufsTer3
NM_000109.4:c.3573_3577del	NP_000100.3:p.Met1192GlufsTer3
NM_004006.3:c.3597_3601del MANE Select	NP_003997.2:p.Met1200GlufsTer3