Canonical Allele Identifier: CA2695232121

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32697878_32697881delinsATT , CM000685.2:g.32697878_32697881delinsATT	GRCh38
NC_000023.10:g.32715995_32715998delinsATT , CM000685.1:g.32715995_32715998delinsATT	GRCh37
NC_000023.9:g.32625916_32625919delinsATT	NCBI36
NG_012232.1:g.646729_646732delinsAAT , LRG_199:g.646729_646732delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682071.1:c.580_583delinsAAT	ENSP00000508133.1:p.Phe194AsnfsTer18
ENST00000682870.1:n.1134_1137delinsAAT
ENST00000682899.1:n.1156_1159delinsAAT
ENST00000682924.1:c.949_952delinsAAT	ENSP00000508187.1:p.Phe317AsnfsTer18
ENST00000683985.1:n.1156_1159delinsAAT
ENST00000684165.1:n.1156_1159delinsAAT
ENST00000684237.1:c.831+1231_831+1234delinsAAT	ENSP00000507277.1:n.831+1231_831+1234delinsAAT
ENST00000684292.1:n.1156_1159delinsAAT
ENST00000288447.9:c.925_928delinsAAT	ENSP00000288447.4:p.Phe309AsnfsTer18
ENST00000357033.9:c.949_952delinsAAT MANE Select	ENSP00000354923.3:p.Phe317AsnfsTer18
ENST00000288447.8:c.925_928delinsAAT	ENSP00000288447.4:p.Phe309AsnfsTer18
ENST00000357033.8:c.949_952delinsAAT	ENSP00000354923.3:p.Phe317AsnfsTer18
ENST00000378677.6:c.937_940delinsAAT	ENSP00000367948.2:p.Phe313AsnfsTer18
ENST00000420596.5:c.93+322258_93+322261delinsAAT	ENSP00000399897.1:n.93+322258_93+322261delinsAAT
ENST00000447523.1:c.247-124035_247-124032delinsAAT	ENSP00000395904.1:n.247-124035_247-124032delinsAAT
ENST00000448370.5:c.93+322258_93+322261delinsAAT	ENSP00000388559.1:n.93+322258_93+322261delinsAAT
ENST00000480751.1:n.86+118587_86+118590delinsAAT
ENST00000488902.5:n.335+322258_335+322261delinsAAT
ENST00000619831.4:c.937_940delinsAAT	ENSP00000479270.1:p.Phe313AsnfsTer18
ENST00000620040.4:c.949_952delinsAAT	ENSP00000478150.1:p.Phe317AsnfsTer18
NM_000109.3:c.925_928delinsAAT	NP_000100.2:p.Phe309AsnfsTer18
NM_004006.2:c.949_952delinsAAT , LRG_199t1:c.949_952delinsAAT	NP_003997.1:p.Phe317AsnfsTer18
NM_004009.3:c.937_940delinsAAT	NP_004000.1:p.Phe313AsnfsTer18
NM_004010.3:c.580_583delinsAAT	NP_004001.1:p.Phe194AsnfsTer18
XM_006724468.2:c.949_952delinsAAT	XP_006724531.1:p.Phe317AsnfsTer18
XM_006724469.2:c.925_928delinsAAT	XP_006724532.1:p.Phe309AsnfsTer18
XM_006724470.2:c.949_952delinsAAT	XP_006724533.1:p.Phe317AsnfsTer18
XM_006724471.2:c.949_952delinsAAT	XP_006724534.1:p.Phe317AsnfsTer18
XM_006724472.2:c.831+1231_831+1234delinsAAT	XP_006724535.1:n.831+1231_831+1234delinsAAT
XM_006724473.2:c.949_952delinsAAT	XP_006724536.1:p.Phe317AsnfsTer18
XM_006724474.2:c.949_952delinsAAT	XP_006724537.1:p.Phe317AsnfsTer18
XM_006724475.2:c.949_952delinsAAT	XP_006724538.1:p.Phe317AsnfsTer18
XM_011545467.1:c.949_952delinsAAT	XP_011543769.1:p.Phe317AsnfsTer18
XM_011545468.1:c.949_952delinsAAT	XP_011543770.1:p.Phe317AsnfsTer18
XM_011545469.1:c.949_952delinsAAT	XP_011543771.1:p.Phe317AsnfsTer18
XM_006724469.3:c.925_928delinsAAT	XP_006724532.1:p.Phe309AsnfsTer18
XM_006724470.3:c.949_952delinsAAT	XP_006724533.1:p.Phe317AsnfsTer18
XM_006724474.3:c.949_952delinsAAT	XP_006724537.1:p.Phe317AsnfsTer18
XM_011545468.2:c.949_952delinsAAT	XP_011543770.1:p.Phe317AsnfsTer18
XM_017029328.1:c.949_952delinsAAT	XP_016884817.1:p.Phe317AsnfsTer18
XM_017029329.1:c.949_952delinsAAT	XP_016884818.1:p.Phe317AsnfsTer18
XM_017029330.2:c.949_952delinsAAT	XP_016884819.1:p.Phe317AsnfsTer18
NM_000109.4:c.925_928delinsAAT	NP_000100.3:p.Phe309AsnfsTer18
NM_004006.3:c.949_952delinsAAT MANE Select	NP_003997.2:p.Phe317AsnfsTer18