Canonical Allele Identifier: CA2693396059

Gene: DMD

Linked Data

• gnomAD v4: X-32454644-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32454646_32454647del , CM000685.2:g.32454646_32454647del	GRCh38
NC_000023.10:g.32472763_32472764del , CM000685.1:g.32472763_32472764del	GRCh37
NC_000023.9:g.32382684_32382685del	NCBI36
NG_012232.1:g.889964_889965del , LRG_199:g.889964_889965del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682899.1:n.3810+16_3810+17del
ENST00000357033.9:c.3603+16_3603+17del MANE Select	ENSP00000354923.3:n.3603+16_3603+17del
ENST00000357033.8:c.3603+16_3603+17del	ENSP00000354923.3:n.3603+16_3603+17del
ENST00000378677.6:c.3591+16_3591+17del	ENSP00000367948.2:n.3591+16_3591+17del
ENST00000420596.5:c.94-89447_94-89446del	ENSP00000399897.1:n.94-89447_94-89446del
ENST00000448370.5:c.94-89936_94-89935del	ENSP00000388559.1:n.94-89936_94-89935del
ENST00000488902.5:n.336-237583_336-237582del
ENST00000619831.4:c.3591+16_3591+17del	ENSP00000479270.1:n.3591+16_3591+17del
ENST00000620040.4:c.3603+16_3603+17del	ENSP00000478150.1:n.3603+16_3603+17del
NM_000109.3:c.3579+16_3579+17del	NP_000100.2:n.3579+16_3579+17del
NM_004006.2:c.3603+16_3603+17del , LRG_199t1:c.3603+16_3603+17del	NP_003997.1:n.3603+16_3603+17del
NM_004009.3:c.3591+16_3591+17del	NP_004000.1:n.3591+16_3591+17del
NM_004010.3:c.3234+16_3234+17del	NP_004001.1:n.3234+16_3234+17del
XM_006724468.2:c.3603+16_3603+17del	XP_006724531.1:n.3603+16_3603+17del
XM_006724469.2:c.3579+16_3579+17del	XP_006724532.1:n.3579+16_3579+17del
XM_006724470.2:c.3603+16_3603+17del	XP_006724533.1:n.3603+16_3603+17del
XM_006724471.2:c.3603+16_3603+17del	XP_006724534.1:n.3603+16_3603+17del
XM_006724472.2:c.3474+16_3474+17del	XP_006724535.1:n.3474+16_3474+17del
XM_006724473.2:c.3603+16_3603+17del	XP_006724536.1:n.3603+16_3603+17del
XM_006724474.2:c.3603+16_3603+17del	XP_006724537.1:n.3603+16_3603+17del
XM_006724475.2:c.3603+16_3603+17del	XP_006724538.1:n.3603+16_3603+17del
XM_011545467.1:c.3603+16_3603+17del	XP_011543769.1:n.3603+16_3603+17del
XM_011545468.1:c.3603+16_3603+17del	XP_011543770.1:n.3603+16_3603+17del
XM_011545469.1:c.3603+16_3603+17del	XP_011543771.1:n.3603+16_3603+17del
XM_006724469.3:c.3579+16_3579+17del	XP_006724532.1:n.3579+16_3579+17del
XM_006724470.3:c.3603+16_3603+17del	XP_006724533.1:n.3603+16_3603+17del
XM_006724474.3:c.3603+16_3603+17del	XP_006724537.1:n.3603+16_3603+17del
XM_011545468.2:c.3603+16_3603+17del	XP_011543770.1:n.3603+16_3603+17del
XM_017029328.1:c.3603+16_3603+17del	XP_016884817.1:n.3603+16_3603+17del
XM_017029329.1:c.3603+16_3603+17del	XP_016884818.1:n.3603+16_3603+17del
XM_017029330.2:c.3603+16_3603+17del	XP_016884819.1:n.3603+16_3603+17del
NM_000109.4:c.3579+16_3579+17del	NP_000100.3:n.3579+16_3579+17del
NM_004006.3:c.3603+16_3603+17del MANE Select	NP_003997.2:n.3603+16_3603+17del