Canonical Allele Identifier: CA10378138

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31627753T>C , CM000685.2:g.31627753T>C	GRCh38
NC_000023.10:g.31645870T>C , CM000685.1:g.31645870T>C	GRCh37
NC_000023.9:g.31555791T>C	NCBI36
NG_012232.1:g.1716857A>G , LRG_199:g.1716857A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004006.3:c.8137A>G MANE Select	NP_003997.2:p.Asn2713Asp
ENST00000357033.9:c.8137A>G MANE Select	ENSP00000354923.3:p.Asn2713Asp
NM_000109.3:c.8113A>G	NP_000100.2:p.Asn2705Asp
NM_000109.4:c.8113A>G	NP_000100.3:p.Asn2705Asp
NM_004006.2:c.8137A>G , LRG_199t1:c.8137A>G	NP_003997.1:p.Asn2713Asp
NM_004009.3:c.8125A>G	NP_004000.1:p.Asn2709Asp
NM_004010.3:c.7768A>G	NP_004001.1:p.Asn2590Asp
NM_004011.3:c.4114A>G	NP_004002.2:p.Asn1372Asp
NM_004011.4:c.4114A>G	NP_004002.3:p.Asn1372Asp
NM_004012.3:c.4105A>G	NP_004003.1:p.Asn1369Asp
NM_004012.4:c.4105A>G	NP_004003.2:p.Asn1369Asp
NM_004013.2:c.757A>G	NP_004004.1:p.Asn253Asp
NM_004013.3:c.757A>G	NP_004004.2:p.Asn253Asp
NM_004020.3:c.757A>G	NP_004011.2:p.Asn253Asp
NM_004020.4:c.757A>G	NP_004011.3:p.Asn253Asp
NM_004021.2:c.757A>G	NP_004012.1:p.Asn253Asp
NM_004021.3:c.757A>G	NP_004012.2:p.Asn253Asp
NM_004022.2:c.757A>G	NP_004013.1:p.Asn253Asp
NM_004022.3:c.757A>G	NP_004013.2:p.Asn253Asp
NM_004023.2:c.757A>G	NP_004014.1:p.Asn253Asp
NM_004023.3:c.757A>G	NP_004014.2:p.Asn253Asp
ENST00000357033.8:c.8137A>G	ENSP00000354923.3:p.Asn2713Asp
ENST00000358062.6:c.1225A>G	ENSP00000350765.2:p.Asn409Asp
ENST00000358062.7:c.2983A>G	ENSP00000350765.3:p.Asn995Asp
ENST00000359836.5:c.757A>G	ENSP00000352894.1:p.Asn253Asp
ENST00000378677.6:c.8125A>G	ENSP00000367948.2:p.Asn2709Asp
ENST00000378707.7:c.757A>G	ENSP00000367979.3:p.Asn253Asp
ENST00000474231.5:c.757A>G	ENSP00000417123.1:p.Asn253Asp
ENST00000541735.5:c.757A>G	ENSP00000444119.1:p.Asn253Asp
ENST00000619831.4:c.8122A>G	ENSP00000479270.1:p.Asn2708Asp
ENST00000619831.5:c.4105A>G	ENSP00000479270.2:p.Asn1369Asp
ENST00000620040.4:c.8134A>G	ENSP00000478150.1:p.Asn2712Asp
ENST00000620040.5:c.757A>G	ENSP00000478150.2:p.Asn253Asp
ENST00000680961.1:c.757A>G	ENSP00000506386.1:p.Asn253Asp
ENST00000681646.1:n.1798A>G
ENST00000682238.1:c.757A>G	ENSP00000508124.1:p.Asn253Asp
ENST00000683450.1:n.1602A>G
ENST00000683851.1:n.1798A>G
ENST00000683957.1:n.1629A>G
ENST00000684130.1:c.757A>G	ENSP00000508037.1:p.Asn253Asp
XM_006724468.2:c.8137A>G	XP_006724531.1:p.Asn2713Asp
XM_006724469.2:c.8113A>G	XP_006724532.1:p.Asn2705Asp
XM_006724469.3:c.8113A>G	XP_006724532.1:p.Asn2705Asp
XM_006724470.2:c.8137A>G	XP_006724533.1:p.Asn2713Asp
XM_006724470.3:c.8137A>G	XP_006724533.1:p.Asn2713Asp
XM_006724471.2:c.8137A>G	XP_006724534.1:p.Asn2713Asp
XM_006724472.2:c.8008A>G	XP_006724535.1:p.Asn2670Asp
XM_006724473.2:c.7999A>G	XP_006724536.1:p.Asn2667Asp
XM_006724474.2:c.8137A>G	XP_006724537.1:p.Asn2713Asp
XM_006724474.3:c.8137A>G	XP_006724537.1:p.Asn2713Asp
XM_006724475.2:c.8137A>G	XP_006724538.1:p.Asn2713Asp
XM_011545467.1:c.8014A>G	XP_011543769.1:p.Asn2672Asp
XM_011545468.1:c.8137A>G	XP_011543770.1:p.Asn2713Asp
XM_011545468.2:c.8137A>G	XP_011543770.1:p.Asn2713Asp
XM_017029328.1:c.8137A>G	XP_016884817.1:p.Asn2713Asp
XM_017029331.1:c.2311A>G	XP_016884820.1:p.Asn771Asp