Canonical Allele Identifier: CA341061
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 11255
ClinVar RCV Id: RCV000012006
dbSNP Id: rs128626246

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32464674C>T , CM000685.2:g.32464674C>T GRCh38
NC_000023.10:g.32482791C>T , CM000685.1:g.32482791C>T GRCh37
NC_000023.9:g.32392712C>T NCBI36
NG_012232.1:g.879936G>A , LRG_199:g.879936G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682899.1:n.3395G>A
ENST00000357033.9:c.3188G>A MANE Select ENSP00000354923.3:p.Trp1063Ter
ENST00000357033.8:c.3188G>A ENSP00000354923.3:p.Trp1063Ter
ENST00000378677.6:c.3176G>A ENSP00000367948.2:p.Trp1059Ter
ENST00000420596.5:c.94-99475G>A ENSP00000399897.1:n.94-99475G>A
ENST00000448370.5:c.94-99964G>A ENSP00000388559.1:n.94-99964G>A
ENST00000488902.5:n.336-247611G>A
ENST00000619831.4:c.3176G>A ENSP00000479270.1:p.Trp1059Ter
ENST00000620040.4:c.3188G>A ENSP00000478150.1:p.Trp1063Ter
NM_000109.3:c.3164G>A NP_000100.2:p.Trp1055Ter
NM_004006.2:c.3188G>A , LRG_199t1:c.3188G>A NP_003997.1:p.Trp1063Ter
NM_004009.3:c.3176G>A NP_004000.1:p.Trp1059Ter
NM_004010.3:c.2819G>A NP_004001.1:p.Trp940Ter
XM_006724468.2:c.3188G>A XP_006724531.1:p.Trp1063Ter
XM_006724469.2:c.3164G>A XP_006724532.1:p.Trp1055Ter
XM_006724470.2:c.3188G>A XP_006724533.1:p.Trp1063Ter
XM_006724471.2:c.3188G>A XP_006724534.1:p.Trp1063Ter
XM_006724472.2:c.3059G>A XP_006724535.1:p.Trp1020Ter
XM_006724473.2:c.3188G>A XP_006724536.1:p.Trp1063Ter
XM_006724474.2:c.3188G>A XP_006724537.1:p.Trp1063Ter
XM_006724475.2:c.3188G>A XP_006724538.1:p.Trp1063Ter
XM_011545467.1:c.3188G>A XP_011543769.1:p.Trp1063Ter
XM_011545468.1:c.3188G>A XP_011543770.1:p.Trp1063Ter
XM_011545469.1:c.3188G>A XP_011543771.1:p.Trp1063Ter
XM_006724469.3:c.3164G>A XP_006724532.1:p.Trp1055Ter
XM_006724470.3:c.3188G>A XP_006724533.1:p.Trp1063Ter
XM_006724474.3:c.3188G>A XP_006724537.1:p.Trp1063Ter
XM_011545468.2:c.3188G>A XP_011543770.1:p.Trp1063Ter
XM_017029328.1:c.3188G>A XP_016884817.1:p.Trp1063Ter
XM_017029329.1:c.3188G>A XP_016884818.1:p.Trp1063Ter
XM_017029330.2:c.3188G>A XP_016884819.1:p.Trp1063Ter
NM_000109.4:c.3164G>A NP_000100.3:p.Trp1055Ter
NM_004006.3:c.3188G>A MANE Select NP_003997.2:p.Trp1063Ter