Canonical Allele Identifier: CA267127
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 94758
ClinVar RCV Id: RCV000080751
dbSNP Id: rs398124042

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.31836729G>A , CM000685.2:g.31836729G>A GRCh38
NC_000023.10:g.31854846G>A , CM000685.1:g.31854846G>A GRCh37
NC_000023.9:g.31764767G>A NCBI36
NG_012232.1:g.1507881C>T , LRG_199:g.1507881C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000358062.7:c.2035C>T ENSP00000350765.3:p.Gln679Ter
ENST00000682238.1:c.-192C>T ENSP00000508124.1:n.-192C>T
ENST00000683117.1:n.850C>T
ENST00000683450.1:n.772C>T
ENST00000683851.1:n.850C>T
ENST00000683957.1:n.681C>T
ENST00000684130.1:c.-192C>T ENSP00000508037.1:n.-192C>T
ENST00000357033.9:c.7189C>T MANE Select ENSP00000354923.3:p.Gln2397Ter
ENST00000619831.5:c.3157C>T ENSP00000479270.2:p.Gln1053Ter
ENST00000620040.5:c.-192C>T ENSP00000478150.2:n.-192C>T
ENST00000680961.1:c.-192C>T ENSP00000506386.1:n.-192C>T
ENST00000681646.1:n.850C>T
ENST00000681839.1:c.178C>T ENSP00000505228.1:p.Gln60Ter
ENST00000357033.8:c.7189C>T ENSP00000354923.3:p.Gln2397Ter
ENST00000358062.6:c.277C>T ENSP00000350765.2:p.Gln93Ter
ENST00000359836.5:c.-192C>T ENSP00000352894.1:n.-192C>T
ENST00000378677.6:c.7177C>T ENSP00000367948.2:p.Gln2393Ter
ENST00000378707.7:c.-192C>T ENSP00000367979.3:n.-192C>T
ENST00000471779.1:c.55C>T ENSP00000417075.1:p.Gln19Ter
ENST00000474231.5:c.-192C>T ENSP00000417123.1:n.-192C>T
ENST00000541735.5:c.-192C>T ENSP00000444119.1:n.-192C>T
ENST00000619831.4:c.7174C>T ENSP00000479270.1:p.Gln2392Ter
ENST00000620040.4:c.7186C>T ENSP00000478150.1:p.Gln2396Ter
NM_000109.3:c.7165C>T NP_000100.2:p.Gln2389Ter
NM_004006.2:c.7189C>T , LRG_199t1:c.7189C>T NP_003997.1:p.Gln2397Ter
NM_004009.3:c.7177C>T NP_004000.1:p.Gln2393Ter
NM_004010.3:c.6820C>T NP_004001.1:p.Gln2274Ter
NM_004011.3:c.3166C>T NP_004002.2:p.Gln1056Ter
NM_004012.3:c.3157C>T NP_004003.1:p.Gln1053Ter
NM_004013.2:c.-192C>T NP_004004.1:n.-192C>T
NM_004020.3:c.-192C>T NP_004011.2:n.-192C>T
NM_004021.2:c.-192C>T NP_004012.1:n.-192C>T
NM_004022.2:c.-192C>T NP_004013.1:n.-192C>T
NM_004023.2:c.-192C>T NP_004014.1:n.-192C>T
XM_006724468.2:c.7189C>T XP_006724531.1:p.Gln2397Ter
XM_006724469.2:c.7165C>T XP_006724532.1:p.Gln2389Ter
XM_006724470.2:c.7189C>T XP_006724533.1:p.Gln2397Ter
XM_006724471.2:c.7189C>T XP_006724534.1:p.Gln2397Ter
XM_006724472.2:c.7060C>T XP_006724535.1:p.Gln2354Ter
XM_006724473.2:c.7051C>T XP_006724536.1:p.Gln2351Ter
XM_006724474.2:c.7189C>T XP_006724537.1:p.Gln2397Ter
XM_006724475.2:c.7189C>T XP_006724538.1:p.Gln2397Ter
XM_011545467.1:c.7066C>T XP_011543769.1:p.Gln2356Ter
XM_011545468.1:c.7189C>T XP_011543770.1:p.Gln2397Ter
XM_006724469.3:c.7165C>T XP_006724532.1:p.Gln2389Ter
XM_006724470.3:c.7189C>T XP_006724533.1:p.Gln2397Ter
XM_006724474.3:c.7189C>T XP_006724537.1:p.Gln2397Ter
XM_011545468.2:c.7189C>T XP_011543770.1:p.Gln2397Ter
XM_017029328.1:c.7189C>T XP_016884817.1:p.Gln2397Ter
XM_017029331.1:c.1363C>T XP_016884820.1:p.Gln455Ter
NM_000109.4:c.7165C>T NP_000100.3:p.Gln2389Ter
NM_004006.3:c.7189C>T MANE Select NP_003997.2:p.Gln2397Ter
NM_004011.4:c.3166C>T NP_004002.3:p.Gln1056Ter
NM_004012.4:c.3157C>T NP_004003.2:p.Gln1053Ter
NM_004021.3:c.-192C>T NP_004012.2:n.-192C>T
NM_004023.3:c.-192C>T NP_004014.2:n.-192C>T
NM_004013.3:c.-192C>T NP_004004.2:n.-192C>T
NM_004020.4:c.-192C>T NP_004011.3:n.-192C>T
NM_004022.3:c.-192C>T NP_004013.2:n.-192C>T