Canonical Allele Identifier: CA412669873
Gene: DMD HGNC NCBI

Linked Data

gnomAD v4: X-32310195-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32310195T>A , CM000685.2:g.32310195T>A GRCh38
NC_000023.10:g.32328312T>A , CM000685.1:g.32328312T>A GRCh37
NC_000023.9:g.32238233T>A NCBI36
NG_012232.1:g.1034415A>T , LRG_199:g.1034415A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000358062.7:c.850A>T ENSP00000350765.3:p.Thr284Ser
ENST00000357033.9:c.6004A>T MANE Select ENSP00000354923.3:p.Thr2002Ser
ENST00000619831.5:c.1972A>T ENSP00000479270.2:p.Thr658Ser
ENST00000357033.8:c.6004A>T ENSP00000354923.3:p.Thr2002Ser
ENST00000378677.6:c.5992A>T ENSP00000367948.2:p.Thr1998Ser
ENST00000488902.5:n.336-93132A>T
ENST00000619831.4:c.5992A>T ENSP00000479270.1:p.Thr1998Ser
ENST00000620040.4:c.6004A>T ENSP00000478150.1:p.Thr2002Ser
NM_000109.3:c.5980A>T NP_000100.2:p.Thr1994Ser
NM_004006.2:c.6004A>T , LRG_199t1:c.6004A>T NP_003997.1:p.Thr2002Ser
NM_004009.3:c.5992A>T NP_004000.1:p.Thr1998Ser
NM_004010.3:c.5635A>T NP_004001.1:p.Thr1879Ser
NM_004011.3:c.1981A>T NP_004002.2:p.Thr661Ser
NM_004012.3:c.1972A>T NP_004003.1:p.Thr658Ser
XM_006724468.2:c.6004A>T XP_006724531.1:p.Thr2002Ser
XM_006724469.2:c.5980A>T XP_006724532.1:p.Thr1994Ser
XM_006724470.2:c.6004A>T XP_006724533.1:p.Thr2002Ser
XM_006724471.2:c.6004A>T XP_006724534.1:p.Thr2002Ser
XM_006724472.2:c.5875A>T XP_006724535.1:p.Thr1959Ser
XM_006724473.2:c.5866A>T XP_006724536.1:p.Thr1956Ser
XM_006724474.2:c.6004A>T XP_006724537.1:p.Thr2002Ser
XM_006724475.2:c.6004A>T XP_006724538.1:p.Thr2002Ser
XM_011545467.1:c.5881A>T XP_011543769.1:p.Thr1961Ser
XM_011545468.1:c.6004A>T XP_011543770.1:p.Thr2002Ser
XM_006724469.3:c.5980A>T XP_006724532.1:p.Thr1994Ser
XM_006724470.3:c.6004A>T XP_006724533.1:p.Thr2002Ser
XM_006724474.3:c.6004A>T XP_006724537.1:p.Thr2002Ser
XM_011545468.2:c.6004A>T XP_011543770.1:p.Thr2002Ser
XM_017029328.1:c.6004A>T XP_016884817.1:p.Thr2002Ser
XM_017029329.1:c.6004A>T XP_016884818.1:p.Thr2002Ser
XM_017029330.2:c.6004A>T XP_016884819.1:p.Thr2002Ser
XM_017029331.1:c.178A>T XP_016884820.1:p.Thr60Ser
NM_000109.4:c.5980A>T NP_000100.3:p.Thr1994Ser
NM_004006.3:c.6004A>T MANE Select NP_003997.2:p.Thr2002Ser
NM_004011.4:c.1981A>T NP_004002.3:p.Thr661Ser
NM_004012.4:c.1972A>T NP_004003.2:p.Thr658Ser