Canonical Allele Identifier: CA874708473

Gene: DMD

Linked Data

• dbSNP Id: rs1259957372
• gnomAD v4: X-32364880-ATATTGT-A
• MyVariant Identifiers: chrX:g.32382998_32383003del (hg19) ; chrX:g.32364881_32364886del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32364884_32364889del , CM000685.2:g.32364884_32364889del	GRCh38
NC_000023.10:g.32383001_32383006del , CM000685.1:g.32383001_32383006del	GRCh37
NC_000023.9:g.32292922_32292927del	NCBI36
NG_012232.1:g.979724_979729del , LRG_199:g.979724_979729del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357033.9:c.5025+134_5025+139del MANE Select	ENSP00000354923.3:n.5025+134_5025+139del
ENST00000619831.5:c.993+134_993+139del	ENSP00000479270.2:n.993+134_993+139del
ENST00000357033.8:c.5025+134_5025+139del	ENSP00000354923.3:n.5025+134_5025+139del
ENST00000378677.6:c.5013+134_5013+139del	ENSP00000367948.2:n.5013+134_5013+139del
ENST00000420596.5:c.273+134_273+139del	ENSP00000399897.1:n.273+134_273+139del
ENST00000448370.5:c.94-176_94-171del	ENSP00000388559.1:n.94-176_94-171del
ENST00000488902.5:n.336-147823_336-147818del
ENST00000619831.4:c.5013+134_5013+139del	ENSP00000479270.1:n.5013+134_5013+139del
ENST00000620040.4:c.5025+134_5025+139del	ENSP00000478150.1:n.5025+134_5025+139del
NM_000109.3:c.5001+134_5001+139del	NP_000100.2:n.5001+134_5001+139del
NM_004006.2:c.5025+134_5025+139del , LRG_199t1:c.5025+134_5025+139del	NP_003997.1:n.5025+134_5025+139del
NM_004009.3:c.5013+134_5013+139del	NP_004000.1:n.5013+134_5013+139del
NM_004010.3:c.4656+134_4656+139del	NP_004001.1:n.4656+134_4656+139del
NM_004011.3:c.1002+134_1002+139del	NP_004002.2:n.1002+134_1002+139del
NM_004012.3:c.993+134_993+139del	NP_004003.1:n.993+134_993+139del
XM_006724468.2:c.5025+134_5025+139del	XP_006724531.1:n.5025+134_5025+139del
XM_006724469.2:c.5001+134_5001+139del	XP_006724532.1:n.5001+134_5001+139del
XM_006724470.2:c.5025+134_5025+139del	XP_006724533.1:n.5025+134_5025+139del
XM_006724471.2:c.5025+134_5025+139del	XP_006724534.1:n.5025+134_5025+139del
XM_006724472.2:c.4896+134_4896+139del	XP_006724535.1:n.4896+134_4896+139del
XM_006724473.2:c.5025+134_5025+139del	XP_006724536.1:n.5025+134_5025+139del
XM_006724474.2:c.5025+134_5025+139del	XP_006724537.1:n.5025+134_5025+139del
XM_006724475.2:c.5025+134_5025+139del	XP_006724538.1:n.5025+134_5025+139del
XM_011545467.1:c.5025+134_5025+139del	XP_011543769.1:n.5025+134_5025+139del
XM_011545468.1:c.5025+134_5025+139del	XP_011543770.1:n.5025+134_5025+139del
XM_011545469.1:c.5025+134_5025+139del	XP_011543771.1:n.5025+134_5025+139del
XM_006724469.3:c.5001+134_5001+139del	XP_006724532.1:n.5001+134_5001+139del
XM_006724470.3:c.5025+134_5025+139del	XP_006724533.1:n.5025+134_5025+139del
XM_006724474.3:c.5025+134_5025+139del	XP_006724537.1:n.5025+134_5025+139del
XM_011545468.2:c.5025+134_5025+139del	XP_011543770.1:n.5025+134_5025+139del
XM_017029328.1:c.5025+134_5025+139del	XP_016884817.1:n.5025+134_5025+139del
XM_017029329.1:c.5025+134_5025+139del	XP_016884818.1:n.5025+134_5025+139del
XM_017029330.2:c.5025+134_5025+139del	XP_016884819.1:n.5025+134_5025+139del
NM_000109.4:c.5001+134_5001+139del	NP_000100.3:n.5001+134_5001+139del
NM_004006.3:c.5025+134_5025+139del MANE Select	NP_003997.2:n.5025+134_5025+139del
NM_004011.4:c.1002+134_1002+139del	NP_004002.3:n.1002+134_1002+139del
NM_004012.4:c.993+134_993+139del	NP_004003.2:n.993+134_993+139del