Canonical Allele Identifier: CA2580100605

Gene: DMD

Linked Data

• ClinVar Variation Id: 2020179
• ClinVar RCV Id: RCV002866014

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31774076del , CM000685.2:g.31774076del	GRCh38
NC_000023.10:g.31792193del , CM000685.1:g.31792193del	GRCh37
NC_000023.9:g.31702114del	NCBI36
NG_012232.1:g.1570535del , LRG_199:g.1570535del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.2273del	ENSP00000350765.3:p.Asn758ThrfsTer18
ENST00000682238.1:c.47del	ENSP00000508124.1:p.Asn16ThrfsTer18
ENST00000683117.1:n.1088del
ENST00000683450.1:n.1010del
ENST00000683851.1:n.1088del
ENST00000683957.1:n.919del
ENST00000684130.1:c.47del	ENSP00000508037.1:p.Asn16ThrfsTer18
ENST00000357033.9:c.7427del MANE Select	ENSP00000354923.3:p.Asn2476ThrfsTer18
ENST00000619831.5:c.3395del	ENSP00000479270.2:p.Asn1132ThrfsTer18
ENST00000620040.5:c.47del	ENSP00000478150.2:p.Asn16ThrfsTer18
ENST00000680961.1:c.47del	ENSP00000506386.1:p.Asn16ThrfsTer18
ENST00000681646.1:n.1088del
ENST00000681839.1:c.416del	ENSP00000505228.1:p.Asn139ThrfsTer18
ENST00000357033.8:c.7427del	ENSP00000354923.3:p.Asn2476ThrfsTer18
ENST00000358062.6:c.515del	ENSP00000350765.2:p.Asn172ThrfsTer18
ENST00000359836.5:c.47del	ENSP00000352894.1:p.Asn16ThrfsTer18
ENST00000378677.6:c.7415del	ENSP00000367948.2:p.Asn2472ThrfsTer18
ENST00000378707.7:c.47del	ENSP00000367979.3:p.Asn16ThrfsTer18
ENST00000471779.1:c.184del	ENSP00000417075.1:n.184del
ENST00000474231.5:c.47del	ENSP00000417123.1:p.Asn16ThrfsTer18
ENST00000541735.5:c.47del	ENSP00000444119.1:p.Asn16ThrfsTer18
ENST00000619831.4:c.7412del	ENSP00000479270.1:p.Asn2471ThrfsTer18
ENST00000620040.4:c.7424del	ENSP00000478150.1:p.Asn2475ThrfsTer18
NM_000109.3:c.7403del	NP_000100.2:p.Asn2468ThrfsTer18
NM_004006.2:c.7427del , LRG_199t1:c.7427del	NP_003997.1:p.Asn2476ThrfsTer18
NM_004009.3:c.7415del	NP_004000.1:p.Asn2472ThrfsTer18
NM_004010.3:c.7058del	NP_004001.1:p.Asn2353ThrfsTer18
NM_004011.3:c.3404del	NP_004002.2:p.Asn1135ThrfsTer18
NM_004012.3:c.3395del	NP_004003.1:p.Asn1132ThrfsTer18
NM_004013.2:c.47del	NP_004004.1:p.Asn16ThrfsTer18
NM_004020.3:c.47del	NP_004011.2:p.Asn16ThrfsTer18
NM_004021.2:c.47del	NP_004012.1:p.Asn16ThrfsTer18
NM_004022.2:c.47del	NP_004013.1:p.Asn16ThrfsTer18
NM_004023.2:c.47del	NP_004014.1:p.Asn16ThrfsTer18
XM_006724468.2:c.7427del	XP_006724531.1:p.Asn2476ThrfsTer18
XM_006724469.2:c.7403del	XP_006724532.1:p.Asn2468ThrfsTer18
XM_006724470.2:c.7427del	XP_006724533.1:p.Asn2476ThrfsTer18
XM_006724471.2:c.7427del	XP_006724534.1:p.Asn2476ThrfsTer18
XM_006724472.2:c.7298del	XP_006724535.1:p.Asn2433ThrfsTer18
XM_006724473.2:c.7289del	XP_006724536.1:p.Asn2430ThrfsTer18
XM_006724474.2:c.7427del	XP_006724537.1:p.Asn2476ThrfsTer18
XM_006724475.2:c.7427del	XP_006724538.1:p.Asn2476ThrfsTer18
XM_011545467.1:c.7304del	XP_011543769.1:p.Asn2435ThrfsTer18
XM_011545468.1:c.7427del	XP_011543770.1:p.Asn2476ThrfsTer18
XM_006724469.3:c.7403del	XP_006724532.1:p.Asn2468ThrfsTer18
XM_006724470.3:c.7427del	XP_006724533.1:p.Asn2476ThrfsTer18
XM_006724474.3:c.7427del	XP_006724537.1:p.Asn2476ThrfsTer18
XM_011545468.2:c.7427del	XP_011543770.1:p.Asn2476ThrfsTer18
XM_017029328.1:c.7427del	XP_016884817.1:p.Asn2476ThrfsTer18
XM_017029331.1:c.1601del	XP_016884820.1:p.Asn534ThrfsTer18
NM_000109.4:c.7403del	NP_000100.3:p.Asn2468ThrfsTer18
NM_004006.3:c.7427del MANE Select	NP_003997.2:p.Asn2476ThrfsTer18
NM_004011.4:c.3404del	NP_004002.3:p.Asn1135ThrfsTer18
NM_004012.4:c.3395del	NP_004003.2:p.Asn1132ThrfsTer18
NM_004021.3:c.47del	NP_004012.2:p.Asn16ThrfsTer18
NM_004023.3:c.47del	NP_004014.2:p.Asn16ThrfsTer18
NM_004013.3:c.47del	NP_004004.2:p.Asn16ThrfsTer18
NM_004020.4:c.47del	NP_004011.3:p.Asn16ThrfsTer18
NM_004022.3:c.47del	NP_004013.2:p.Asn16ThrfsTer18