Canonical Allele Identifier: CA874708047

Gene: DMD

Linked Data

• dbSNP Id: rs1426264541
• gnomAD v3: X-32364487-CTCTTAT-C
• gnomAD v4: X-32364487-CTCTTAT-C
• MyVariant Identifiers: chrX:g.32382605_32382610del (hg19) ; chrX:g.32364488_32364493del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32364489_32364494del , CM000685.2:g.32364489_32364494del	GRCh38
NC_000023.10:g.32382606_32382611del , CM000685.1:g.32382606_32382611del	GRCh37
NC_000023.9:g.32292527_32292532del	NCBI36
NG_012232.1:g.980117_980122del , LRG_199:g.980117_980122del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357033.9:c.5154+89_5154+94del MANE Select	ENSP00000354923.3:n.5154+89_5154+94del
ENST00000619831.5:c.1122+89_1122+94del	ENSP00000479270.2:n.1122+89_1122+94del
ENST00000357033.8:c.5154+89_5154+94del	ENSP00000354923.3:n.5154+89_5154+94del
ENST00000378677.6:c.5142+89_5142+94del	ENSP00000367948.2:n.5142+89_5142+94del
ENST00000488902.5:n.336-147430_336-147425del
ENST00000619831.4:c.5142+89_5142+94del	ENSP00000479270.1:n.5142+89_5142+94del
ENST00000620040.4:c.5154+89_5154+94del	ENSP00000478150.1:n.5154+89_5154+94del
NM_000109.3:c.5130+89_5130+94del	NP_000100.2:n.5130+89_5130+94del
NM_004006.2:c.5154+89_5154+94del , LRG_199t1:c.5154+89_5154+94del	NP_003997.1:n.5154+89_5154+94del
NM_004009.3:c.5142+89_5142+94del	NP_004000.1:n.5142+89_5142+94del
NM_004010.3:c.4785+89_4785+94del	NP_004001.1:n.4785+89_4785+94del
NM_004011.3:c.1131+89_1131+94del	NP_004002.2:n.1131+89_1131+94del
NM_004012.3:c.1122+89_1122+94del	NP_004003.1:n.1122+89_1122+94del
XM_006724468.2:c.5154+89_5154+94del	XP_006724531.1:n.5154+89_5154+94del
XM_006724469.2:c.5130+89_5130+94del	XP_006724532.1:n.5130+89_5130+94del
XM_006724470.2:c.5154+89_5154+94del	XP_006724533.1:n.5154+89_5154+94del
XM_006724471.2:c.5154+89_5154+94del	XP_006724534.1:n.5154+89_5154+94del
XM_006724472.2:c.5025+89_5025+94del	XP_006724535.1:n.5025+89_5025+94del
XM_006724473.2:c.5154+89_5154+94del	XP_006724536.1:n.5154+89_5154+94del
XM_006724474.2:c.5154+89_5154+94del	XP_006724537.1:n.5154+89_5154+94del
XM_006724475.2:c.5154+89_5154+94del	XP_006724538.1:n.5154+89_5154+94del
XM_011545467.1:c.5154+89_5154+94del	XP_011543769.1:n.5154+89_5154+94del
XM_011545468.1:c.5154+89_5154+94del	XP_011543770.1:n.5154+89_5154+94del
XM_011545469.1:c.5154+89_5154+94del	XP_011543771.1:n.5154+89_5154+94del
XM_006724469.3:c.5130+89_5130+94del	XP_006724532.1:n.5130+89_5130+94del
XM_006724470.3:c.5154+89_5154+94del	XP_006724533.1:n.5154+89_5154+94del
XM_006724474.3:c.5154+89_5154+94del	XP_006724537.1:n.5154+89_5154+94del
XM_011545468.2:c.5154+89_5154+94del	XP_011543770.1:n.5154+89_5154+94del
XM_017029328.1:c.5154+89_5154+94del	XP_016884817.1:n.5154+89_5154+94del
XM_017029329.1:c.5154+89_5154+94del	XP_016884818.1:n.5154+89_5154+94del
XM_017029330.2:c.5154+89_5154+94del	XP_016884819.1:n.5154+89_5154+94del
NM_000109.4:c.5130+89_5130+94del	NP_000100.3:n.5130+89_5130+94del
NM_004006.3:c.5154+89_5154+94del MANE Select	NP_003997.2:n.5154+89_5154+94del
NM_004011.4:c.1131+89_1131+94del	NP_004002.3:n.1131+89_1131+94del
NM_004012.4:c.1122+89_1122+94del	NP_004003.2:n.1122+89_1122+94del