Canonical Allele Identifier: CA412655148
Gene: DMD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.31444537A>G , CM000685.2:g.31444537A>G GRCh38
NC_000023.10:g.31462654A>G , CM000685.1:g.31462654A>G GRCh37
NC_000023.9:g.31372575A>G NCBI36
NG_012232.1:g.1900073T>C , LRG_199:g.1900073T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358062.7:c.3874T>C ENSP00000350765.3:p.Ser1292Pro
ENST00000682238.1:c.1648T>C ENSP00000508124.1:p.Ser550Pro
ENST00000683450.1:n.2493T>C
ENST00000683957.1:n.2520T>C
ENST00000684130.1:c.1648T>C ENSP00000508037.1:p.Ser550Pro
ENST00000343523.7:c.883T>C ENSP00000340057.4:p.Ser295Pro
ENST00000357033.9:c.9028T>C MANE Select ENSP00000354923.3:p.Ser3010Pro
ENST00000619831.5:c.4996T>C ENSP00000479270.2:p.Ser1666Pro
ENST00000620040.5:c.1648T>C ENSP00000478150.2:p.Ser550Pro
ENST00000680961.1:c.1648T>C ENSP00000506386.1:p.Ser550Pro
ENST00000681646.1:n.2689T>C
ENST00000343523.6:c.841T>C ENSP00000340057.3:p.Ser281Pro
ENST00000357033.8:c.9028T>C ENSP00000354923.3:p.Ser3010Pro
ENST00000358062.6:c.2116T>C ENSP00000350765.2:p.Ser706Pro
ENST00000359836.5:c.1648T>C ENSP00000352894.1:p.Ser550Pro
ENST00000378677.6:c.9016T>C ENSP00000367948.2:p.Ser3006Pro
ENST00000378707.7:c.1648T>C ENSP00000367979.3:p.Ser550Pro
ENST00000474231.5:c.1648T>C ENSP00000417123.1:p.Ser550Pro
ENST00000541735.5:c.1648T>C ENSP00000444119.1:p.Ser550Pro
ENST00000619831.4:c.9013T>C ENSP00000479270.1:p.Ser3005Pro
ENST00000620040.4:c.9025T>C ENSP00000478150.1:p.Ser3009Pro
NM_000109.3:c.9004T>C NP_000100.2:p.Ser3002Pro
NM_004006.2:c.9028T>C , LRG_199t1:c.9028T>C NP_003997.1:p.Ser3010Pro
NM_004009.3:c.9016T>C NP_004000.1:p.Ser3006Pro
NM_004010.3:c.8659T>C NP_004001.1:p.Ser2887Pro
NM_004011.3:c.5005T>C NP_004002.2:p.Ser1669Pro
NM_004012.3:c.4996T>C NP_004003.1:p.Ser1666Pro
NM_004013.2:c.1648T>C NP_004004.1:p.Ser550Pro
NM_004014.2:c.841T>C NP_004005.1:p.Ser281Pro
NM_004020.3:c.1648T>C NP_004011.2:p.Ser550Pro
NM_004021.2:c.1648T>C NP_004012.1:p.Ser550Pro
NM_004022.2:c.1648T>C NP_004013.1:p.Ser550Pro
NM_004023.2:c.1648T>C NP_004014.1:p.Ser550Pro
XM_006724468.2:c.9028T>C XP_006724531.1:p.Ser3010Pro
XM_006724469.2:c.9004T>C XP_006724532.1:p.Ser3002Pro
XM_006724470.2:c.9028T>C XP_006724533.1:p.Ser3010Pro
XM_006724471.2:c.9028T>C XP_006724534.1:p.Ser3010Pro
XM_006724472.2:c.8899T>C XP_006724535.1:p.Ser2967Pro
XM_006724473.2:c.8890T>C XP_006724536.1:p.Ser2964Pro
XM_006724474.2:c.9028T>C XP_006724537.1:p.Ser3010Pro
XM_006724475.2:c.9028T>C XP_006724538.1:p.Ser3010Pro
XM_011545467.1:c.8905T>C XP_011543769.1:p.Ser2969Pro
XM_011545468.1:c.9028T>C XP_011543770.1:p.Ser3010Pro
XM_006724469.3:c.9004T>C XP_006724532.1:p.Ser3002Pro
XM_006724470.3:c.9028T>C XP_006724533.1:p.Ser3010Pro
XM_006724474.3:c.9028T>C XP_006724537.1:p.Ser3010Pro
XM_011545468.2:c.9028T>C XP_011543770.1:p.Ser3010Pro
XM_017029328.1:c.9028T>C XP_016884817.1:p.Ser3010Pro
XM_017029331.1:c.3202T>C XP_016884820.1:p.Ser1068Pro
NM_000109.4:c.9004T>C NP_000100.3:p.Ser3002Pro
NM_004006.3:c.9028T>C MANE Select NP_003997.2:p.Ser3010Pro
NM_004011.4:c.5005T>C NP_004002.3:p.Ser1669Pro
NM_004012.4:c.4996T>C NP_004003.2:p.Ser1666Pro
NM_004021.3:c.1648T>C NP_004012.2:p.Ser550Pro
NM_004023.3:c.1648T>C NP_004014.2:p.Ser550Pro
NM_004013.3:c.1648T>C NP_004004.2:p.Ser550Pro
NM_004014.3:c.841T>C NP_004005.2:p.Ser281Pro
NM_004020.4:c.1648T>C NP_004011.3:p.Ser550Pro
NM_004022.3:c.1648T>C NP_004013.2:p.Ser550Pro