Canonical Allele Identifier: CA341040
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 11239
dbSNP Id: rs128626233

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32849736G>A , CM000685.2:g.32849736G>A GRCh38
NC_000023.10:g.32867853G>A , CM000685.1:g.32867853G>A GRCh37
NC_000023.9:g.32777774G>A NCBI36
NG_012232.1:g.494874C>T , LRG_199:g.494874C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682071.1:c.-192C>T ENSP00000508133.1:n.-192C>T
ENST00000682437.1:n.502C>T
ENST00000682584.1:n.502C>T
ENST00000682870.1:n.363C>T
ENST00000682899.1:n.385C>T
ENST00000682924.1:c.178C>T ENSP00000508187.1:p.Gln60Ter
ENST00000683309.1:n.362C>T
ENST00000683658.1:n.523C>T
ENST00000683985.1:n.385C>T
ENST00000684056.1:n.362C>T
ENST00000684165.1:n.385C>T
ENST00000684237.1:c.178C>T ENSP00000507277.1:p.Gln60Ter
ENST00000684292.1:n.385C>T
ENST00000684357.1:n.362C>T
ENST00000684660.1:n.363C>T
ENST00000288447.9:c.154C>T ENSP00000288447.4:p.Gln52Ter
ENST00000357033.9:c.178C>T MANE Select ENSP00000354923.3:p.Gln60Ter
ENST00000288447.8:c.154C>T ENSP00000288447.4:p.Gln52Ter
ENST00000357033.8:c.178C>T ENSP00000354923.3:p.Gln60Ter
ENST00000378677.6:c.166C>T ENSP00000367948.2:p.Gln56Ter
ENST00000420596.5:c.93+170403C>T ENSP00000399897.1:n.93+170403C>T
ENST00000447523.1:c.67C>T ENSP00000395904.1:p.Gln23Ter
ENST00000448370.5:c.93+170403C>T ENSP00000388559.1:n.93+170403C>T
ENST00000472681.1:n.363C>T
ENST00000488902.5:n.335+170403C>T
ENST00000619831.4:c.166C>T ENSP00000479270.1:p.Gln56Ter
ENST00000620040.4:c.178C>T ENSP00000478150.1:p.Gln60Ter
NM_000109.3:c.154C>T NP_000100.2:p.Gln52Ter
NM_004006.2:c.178C>T , LRG_199t1:c.178C>T NP_003997.1:p.Gln60Ter
NM_004009.3:c.166C>T NP_004000.1:p.Gln56Ter
NM_004010.3:c.-192C>T NP_004001.1:n.-192C>T
XM_006724468.2:c.178C>T XP_006724531.1:p.Gln60Ter
XM_006724469.2:c.154C>T XP_006724532.1:p.Gln52Ter
XM_006724470.2:c.178C>T XP_006724533.1:p.Gln60Ter
XM_006724471.2:c.178C>T XP_006724534.1:p.Gln60Ter
XM_006724472.2:c.178C>T XP_006724535.1:p.Gln60Ter
XM_006724473.2:c.178C>T XP_006724536.1:p.Gln60Ter
XM_006724474.2:c.178C>T XP_006724537.1:p.Gln60Ter
XM_006724475.2:c.178C>T XP_006724538.1:p.Gln60Ter
XM_011545467.1:c.178C>T XP_011543769.1:p.Gln60Ter
XM_011545468.1:c.178C>T XP_011543770.1:p.Gln60Ter
XM_011545469.1:c.178C>T XP_011543771.1:p.Gln60Ter
XM_006724469.3:c.154C>T XP_006724532.1:p.Gln52Ter
XM_006724470.3:c.178C>T XP_006724533.1:p.Gln60Ter
XM_006724474.3:c.178C>T XP_006724537.1:p.Gln60Ter
XM_011545468.2:c.178C>T XP_011543770.1:p.Gln60Ter
XM_017029328.1:c.178C>T XP_016884817.1:p.Gln60Ter
XM_017029329.1:c.178C>T XP_016884818.1:p.Gln60Ter
XM_017029330.2:c.178C>T XP_016884819.1:p.Gln60Ter
NM_000109.4:c.154C>T NP_000100.3:p.Gln52Ter
NM_004006.3:c.178C>T MANE Select NP_003997.2:p.Gln60Ter