Canonical Allele Identifier: CA2820327608

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32454649_32454650insCT , CM000685.2:g.32454649_32454650insCT	GRCh38
NC_000023.10:g.32472766_32472767insCT , CM000685.1:g.32472766_32472767insCT	GRCh37
NC_000023.9:g.32382687_32382688insCT	NCBI36
NG_012232.1:g.889961_889962insGA , LRG_199:g.889961_889962insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682899.1:n.3810+13_3810+14insGA
ENST00000357033.9:c.3603+13_3603+14insGA MANE Select	ENSP00000354923.3:n.3603+13_3603+14insGA
ENST00000357033.8:c.3603+13_3603+14insGA	ENSP00000354923.3:n.3603+13_3603+14insGA
ENST00000378677.6:c.3591+13_3591+14insGA	ENSP00000367948.2:n.3591+13_3591+14insGA
ENST00000420596.5:c.94-89450_94-89449insGA	ENSP00000399897.1:n.94-89450_94-89449insGA
ENST00000448370.5:c.94-89939_94-89938insGA	ENSP00000388559.1:n.94-89939_94-89938insGA
ENST00000488902.5:n.336-237586_336-237585insGA
ENST00000619831.4:c.3591+13_3591+14insGA	ENSP00000479270.1:n.3591+13_3591+14insGA
ENST00000620040.4:c.3603+13_3603+14insGA	ENSP00000478150.1:n.3603+13_3603+14insGA
NM_000109.3:c.3579+13_3579+14insGA	NP_000100.2:n.3579+13_3579+14insGA
NM_004006.2:c.3603+13_3603+14insGA , LRG_199t1:c.3603+13_3603+14insGA	NP_003997.1:n.3603+13_3603+14insGA
NM_004009.3:c.3591+13_3591+14insGA	NP_004000.1:n.3591+13_3591+14insGA
NM_004010.3:c.3234+13_3234+14insGA	NP_004001.1:n.3234+13_3234+14insGA
XM_006724468.2:c.3603+13_3603+14insGA	XP_006724531.1:n.3603+13_3603+14insGA
XM_006724469.2:c.3579+13_3579+14insGA	XP_006724532.1:n.3579+13_3579+14insGA
XM_006724470.2:c.3603+13_3603+14insGA	XP_006724533.1:n.3603+13_3603+14insGA
XM_006724471.2:c.3603+13_3603+14insGA	XP_006724534.1:n.3603+13_3603+14insGA
XM_006724472.2:c.3474+13_3474+14insGA	XP_006724535.1:n.3474+13_3474+14insGA
XM_006724473.2:c.3603+13_3603+14insGA	XP_006724536.1:n.3603+13_3603+14insGA
XM_006724474.2:c.3603+13_3603+14insGA	XP_006724537.1:n.3603+13_3603+14insGA
XM_006724475.2:c.3603+13_3603+14insGA	XP_006724538.1:n.3603+13_3603+14insGA
XM_011545467.1:c.3603+13_3603+14insGA	XP_011543769.1:n.3603+13_3603+14insGA
XM_011545468.1:c.3603+13_3603+14insGA	XP_011543770.1:n.3603+13_3603+14insGA
XM_011545469.1:c.3603+13_3603+14insGA	XP_011543771.1:n.3603+13_3603+14insGA
XM_006724469.3:c.3579+13_3579+14insGA	XP_006724532.1:n.3579+13_3579+14insGA
XM_006724470.3:c.3603+13_3603+14insGA	XP_006724533.1:n.3603+13_3603+14insGA
XM_006724474.3:c.3603+13_3603+14insGA	XP_006724537.1:n.3603+13_3603+14insGA
XM_011545468.2:c.3603+13_3603+14insGA	XP_011543770.1:n.3603+13_3603+14insGA
XM_017029328.1:c.3603+13_3603+14insGA	XP_016884817.1:n.3603+13_3603+14insGA
XM_017029329.1:c.3603+13_3603+14insGA	XP_016884818.1:n.3603+13_3603+14insGA
XM_017029330.2:c.3603+13_3603+14insGA	XP_016884819.1:n.3603+13_3603+14insGA
NM_000109.4:c.3579+13_3579+14insGA	NP_000100.3:n.3579+13_3579+14insGA
NM_004006.3:c.3603+13_3603+14insGA MANE Select	NP_003997.2:n.3603+13_3603+14insGA