Canonical Allele Identifier: CA1132139944

Gene: DMD

Linked Data

• dbSNP Id: rs2098348232
• gnomAD v3: X-32454646-C-CA
• gnomAD v4: X-32454646-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32454646_32454647insA , CM000685.2:g.32454646_32454647insA	GRCh38
NC_000023.10:g.32472763_32472764insA , CM000685.1:g.32472763_32472764insA	GRCh37
NC_000023.9:g.32382684_32382685insA	NCBI36
NG_012232.1:g.889963_889964insT , LRG_199:g.889963_889964insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682899.1:n.3810+15_3810+16insT
ENST00000357033.9:c.3603+15_3603+16insT MANE Select	ENSP00000354923.3:n.3603+15_3603+16insT
ENST00000357033.8:c.3603+15_3603+16insT	ENSP00000354923.3:n.3603+15_3603+16insT
ENST00000378677.6:c.3591+15_3591+16insT	ENSP00000367948.2:n.3591+15_3591+16insT
ENST00000420596.5:c.94-89448_94-89447insT	ENSP00000399897.1:n.94-89448_94-89447insT
ENST00000448370.5:c.94-89937_94-89936insT	ENSP00000388559.1:n.94-89937_94-89936insT
ENST00000488902.5:n.336-237584_336-237583insT
ENST00000619831.4:c.3591+15_3591+16insT	ENSP00000479270.1:n.3591+15_3591+16insT
ENST00000620040.4:c.3603+15_3603+16insT	ENSP00000478150.1:n.3603+15_3603+16insT
NM_000109.3:c.3579+15_3579+16insT	NP_000100.2:n.3579+15_3579+16insT
NM_004006.2:c.3603+15_3603+16insT , LRG_199t1:c.3603+15_3603+16insT	NP_003997.1:n.3603+15_3603+16insT
NM_004009.3:c.3591+15_3591+16insT	NP_004000.1:n.3591+15_3591+16insT
NM_004010.3:c.3234+15_3234+16insT	NP_004001.1:n.3234+15_3234+16insT
XM_006724468.2:c.3603+15_3603+16insT	XP_006724531.1:n.3603+15_3603+16insT
XM_006724469.2:c.3579+15_3579+16insT	XP_006724532.1:n.3579+15_3579+16insT
XM_006724470.2:c.3603+15_3603+16insT	XP_006724533.1:n.3603+15_3603+16insT
XM_006724471.2:c.3603+15_3603+16insT	XP_006724534.1:n.3603+15_3603+16insT
XM_006724472.2:c.3474+15_3474+16insT	XP_006724535.1:n.3474+15_3474+16insT
XM_006724473.2:c.3603+15_3603+16insT	XP_006724536.1:n.3603+15_3603+16insT
XM_006724474.2:c.3603+15_3603+16insT	XP_006724537.1:n.3603+15_3603+16insT
XM_006724475.2:c.3603+15_3603+16insT	XP_006724538.1:n.3603+15_3603+16insT
XM_011545467.1:c.3603+15_3603+16insT	XP_011543769.1:n.3603+15_3603+16insT
XM_011545468.1:c.3603+15_3603+16insT	XP_011543770.1:n.3603+15_3603+16insT
XM_011545469.1:c.3603+15_3603+16insT	XP_011543771.1:n.3603+15_3603+16insT
XM_006724469.3:c.3579+15_3579+16insT	XP_006724532.1:n.3579+15_3579+16insT
XM_006724470.3:c.3603+15_3603+16insT	XP_006724533.1:n.3603+15_3603+16insT
XM_006724474.3:c.3603+15_3603+16insT	XP_006724537.1:n.3603+15_3603+16insT
XM_011545468.2:c.3603+15_3603+16insT	XP_011543770.1:n.3603+15_3603+16insT
XM_017029328.1:c.3603+15_3603+16insT	XP_016884817.1:n.3603+15_3603+16insT
XM_017029329.1:c.3603+15_3603+16insT	XP_016884818.1:n.3603+15_3603+16insT
XM_017029330.2:c.3603+15_3603+16insT	XP_016884819.1:n.3603+15_3603+16insT
NM_000109.4:c.3579+15_3579+16insT	NP_000100.3:n.3579+15_3579+16insT
NM_004006.3:c.3603+15_3603+16insT MANE Select	NP_003997.2:n.3603+15_3603+16insT