Canonical Allele Identifier: CA16043316
Gene: DMD HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 373091
dbSNP Id: rs1057518207

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32545158C>T , CM000685.2:g.32545158C>T GRCh38
NC_000023.10:g.32563275C>T , CM000685.1:g.32563275C>T GRCh37
NC_000023.9:g.32473196C>T NCBI36
NG_012232.1:g.799452G>A , LRG_199:g.799452G>A

Transcript Alleles

HGVS Amino-acid change
NM_000109.3:c.2144+1G>A VV NP_000100.2:p.=
NM_004006.2:c.2168+1G>A , LRG_199t1:c.2168+1G>A NP_003997.1:p.=
NM_004009.3:c.2156+1G>A VV NP_004000.1:p.=
NM_004010.3:c.1799+1G>A VV NP_004001.1:p.=
XM_006724468.2:c.2168+1G>A XP_006724531.1:p.=
XM_006724469.2:c.2144+1G>A XP_006724532.1:p.=
XM_006724470.2:c.2168+1G>A XP_006724533.1:p.=
XM_006724471.2:c.2168+1G>A XP_006724534.1:p.=
XM_006724472.2:c.2039+1G>A XP_006724535.1:p.=
XM_006724473.2:c.2168+1G>A XP_006724536.1:p.=
XM_006724474.2:c.2168+1G>A XP_006724537.1:p.=
XM_006724475.2:c.2168+1G>A XP_006724538.1:p.=
XM_011545467.1:c.2168+1G>A XP_011543769.1:p.=
XM_011545468.1:c.2168+1G>A XP_011543770.1:p.=
XM_011545469.1:c.2168+1G>A XP_011543771.1:p.=
XM_006724469.3:c.2144+1G>A
XM_006724470.3:c.2168+1G>A
XM_006724474.3:c.2168+1G>A
XM_011545468.2:c.2168+1G>A
XM_017029328.1:c.2168+1G>A XP_016884817.1:p.=
XM_017029329.1:c.2168+1G>A XP_016884818.1:p.=
XM_017029330.2:c.2168+1G>A XP_016884819.1:p.=
ENST00000288447.8:c.2144+1G>A ENSP00000288447.4:p.=
ENST00000357033.8:c.2168+1G>A ENSP00000354923.3:p.=
ENST00000378677.6:c.2156+1G>A ENSP00000367948.2:p.=
ENST00000420596.5:n.94-179959G>A ENSP00000399897.1:p.=
ENST00000448370.5:n.94-180448G>A ENSP00000388559.1:p.=
ENST00000488902.5:n.336-328095G>A
ENST00000619831.4:n.2156+1G>A ENSP00000479270.1:p.=
ENST00000620040.4:n.2168+1G>A ENSP00000478150.1:p.=