Canonical Allele Identifier: CA2693396071

Gene: DMD

Linked Data

• gnomAD v4: X-32454652-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32454652_32454653insC , CM000685.2:g.32454652_32454653insC	GRCh38
NC_000023.10:g.32472769_32472770insC , CM000685.1:g.32472769_32472770insC	GRCh37
NC_000023.9:g.32382690_32382691insC	NCBI36
NG_012232.1:g.889957_889958insG , LRG_199:g.889957_889958insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682899.1:n.3810+9_3810+10insG
ENST00000357033.9:c.3603+9_3603+10insG MANE Select	ENSP00000354923.3:n.3603+9_3603+10insG
ENST00000357033.8:c.3603+9_3603+10insG	ENSP00000354923.3:n.3603+9_3603+10insG
ENST00000378677.6:c.3591+9_3591+10insG	ENSP00000367948.2:n.3591+9_3591+10insG
ENST00000420596.5:c.94-89454_94-89453insG	ENSP00000399897.1:n.94-89454_94-89453insG
ENST00000448370.5:c.94-89943_94-89942insG	ENSP00000388559.1:n.94-89943_94-89942insG
ENST00000488902.5:n.336-237590_336-237589insG
ENST00000619831.4:c.3591+9_3591+10insG	ENSP00000479270.1:n.3591+9_3591+10insG
ENST00000620040.4:c.3603+9_3603+10insG	ENSP00000478150.1:n.3603+9_3603+10insG
NM_000109.3:c.3579+9_3579+10insG	NP_000100.2:n.3579+9_3579+10insG
NM_004006.2:c.3603+9_3603+10insG , LRG_199t1:c.3603+9_3603+10insG	NP_003997.1:n.3603+9_3603+10insG
NM_004009.3:c.3591+9_3591+10insG	NP_004000.1:n.3591+9_3591+10insG
NM_004010.3:c.3234+9_3234+10insG	NP_004001.1:n.3234+9_3234+10insG
XM_006724468.2:c.3603+9_3603+10insG	XP_006724531.1:n.3603+9_3603+10insG
XM_006724469.2:c.3579+9_3579+10insG	XP_006724532.1:n.3579+9_3579+10insG
XM_006724470.2:c.3603+9_3603+10insG	XP_006724533.1:n.3603+9_3603+10insG
XM_006724471.2:c.3603+9_3603+10insG	XP_006724534.1:n.3603+9_3603+10insG
XM_006724472.2:c.3474+9_3474+10insG	XP_006724535.1:n.3474+9_3474+10insG
XM_006724473.2:c.3603+9_3603+10insG	XP_006724536.1:n.3603+9_3603+10insG
XM_006724474.2:c.3603+9_3603+10insG	XP_006724537.1:n.3603+9_3603+10insG
XM_006724475.2:c.3603+9_3603+10insG	XP_006724538.1:n.3603+9_3603+10insG
XM_011545467.1:c.3603+9_3603+10insG	XP_011543769.1:n.3603+9_3603+10insG
XM_011545468.1:c.3603+9_3603+10insG	XP_011543770.1:n.3603+9_3603+10insG
XM_011545469.1:c.3603+9_3603+10insG	XP_011543771.1:n.3603+9_3603+10insG
XM_006724469.3:c.3579+9_3579+10insG	XP_006724532.1:n.3579+9_3579+10insG
XM_006724470.3:c.3603+9_3603+10insG	XP_006724533.1:n.3603+9_3603+10insG
XM_006724474.3:c.3603+9_3603+10insG	XP_006724537.1:n.3603+9_3603+10insG
XM_011545468.2:c.3603+9_3603+10insG	XP_011543770.1:n.3603+9_3603+10insG
XM_017029328.1:c.3603+9_3603+10insG	XP_016884817.1:n.3603+9_3603+10insG
XM_017029329.1:c.3603+9_3603+10insG	XP_016884818.1:n.3603+9_3603+10insG
XM_017029330.2:c.3603+9_3603+10insG	XP_016884819.1:n.3603+9_3603+10insG
NM_000109.4:c.3579+9_3579+10insG	NP_000100.3:n.3579+9_3579+10insG
NM_004006.3:c.3603+9_3603+10insG MANE Select	NP_003997.2:n.3603+9_3603+10insG