Canonical Allele Identifier: CA2695232079

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32614449_32614450del , CM000685.2:g.32614449_32614450del	GRCh38
NC_000023.10:g.32632566_32632567del , CM000685.1:g.32632566_32632567del	GRCh37
NC_000023.9:g.32542487_32542488del	NCBI36
NG_012232.1:g.730161_730162del , LRG_199:g.730161_730162del

Transcript Alleles

HGVS	Amino-acid Change
NM_004006.3:c.1336_1337del MANE Select	NP_003997.2:p.His446Ter
ENST00000357033.9:c.1336_1337del MANE Select	ENSP00000354923.3:p.His446Ter
NM_000109.3:c.1312_1313del	NP_000100.2:p.His438Ter
NM_000109.4:c.1312_1313del	NP_000100.3:p.His438Ter
NM_004006.2:c.1336_1337del , LRG_199t1:c.1336_1337del	NP_003997.1:p.His446Ter
NM_004009.3:c.1324_1325del	NP_004000.1:p.His442Ter
NM_004010.3:c.967_968del	NP_004001.1:p.His323Ter
ENST00000288447.8:c.1312_1313del	ENSP00000288447.4:p.His438Ter
ENST00000288447.9:c.1312_1313del	ENSP00000288447.4:p.His438Ter
ENST00000357033.8:c.1336_1337del	ENSP00000354923.3:p.His446Ter
ENST00000378677.6:c.1324_1325del	ENSP00000367948.2:p.His442Ter
ENST00000420596.5:c.94-249250_94-249249del	ENSP00000399897.1:n.94-249250_94-249249del
ENST00000447523.1:c.247-40603_247-40602del	ENSP00000395904.1:n.247-40603_247-40602del
ENST00000448370.5:c.94-249739_94-249738del	ENSP00000388559.1:n.94-249739_94-249738del
ENST00000480751.1:n.87-40603_87-40602del
ENST00000488902.5:n.336-397386_336-397385del
ENST00000619831.4:c.1324_1325del	ENSP00000479270.1:p.His442Ter
ENST00000620040.4:c.1336_1337del	ENSP00000478150.1:p.His446Ter
ENST00000682071.1:c.967_968del	ENSP00000508133.1:p.His323Ter
ENST00000682899.1:n.1543_1544del
ENST00000682924.1:c.1332-18573_1332-18572del	ENSP00000508187.1:n.1332-18573_1332-18572del
ENST00000683985.1:n.1543_1544del
ENST00000684165.1:n.1543_1544del
ENST00000684237.1:c.1207_1208del	ENSP00000507277.1:p.His403Ter
ENST00000684292.1:n.1543_1544del
XM_006724468.2:c.1336_1337del	XP_006724531.1:p.His446Ter
XM_006724469.2:c.1312_1313del	XP_006724532.1:p.His438Ter
XM_006724469.3:c.1312_1313del	XP_006724532.1:p.His438Ter
XM_006724470.2:c.1336_1337del	XP_006724533.1:p.His446Ter
XM_006724470.3:c.1336_1337del	XP_006724533.1:p.His446Ter
XM_006724471.2:c.1336_1337del	XP_006724534.1:p.His446Ter
XM_006724472.2:c.1207_1208del	XP_006724535.1:p.His403Ter
XM_006724473.2:c.1336_1337del	XP_006724536.1:p.His446Ter
XM_006724474.2:c.1336_1337del	XP_006724537.1:p.His446Ter
XM_006724474.3:c.1336_1337del	XP_006724537.1:p.His446Ter
XM_006724475.2:c.1336_1337del	XP_006724538.1:p.His446Ter
XM_011545467.1:c.1336_1337del	XP_011543769.1:p.His446Ter
XM_011545468.1:c.1336_1337del	XP_011543770.1:p.His446Ter
XM_011545468.2:c.1336_1337del	XP_011543770.1:p.His446Ter
XM_011545469.1:c.1336_1337del	XP_011543771.1:p.His446Ter
XM_017029328.1:c.1336_1337del	XP_016884817.1:p.His446Ter
XM_017029329.1:c.1336_1337del	XP_016884818.1:p.His446Ter
XM_017029330.2:c.1336_1337del	XP_016884819.1:p.His446Ter