Canonical Allele Identifier: CA412666024

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32343220G>A , CM000685.2:g.32343220G>A	GRCh38
NC_000023.10:g.32361337G>A , CM000685.1:g.32361337G>A	GRCh37
NC_000023.9:g.32271258G>A	NCBI36
NG_012232.1:g.1001390C>T , LRG_199:g.1001390C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004006.3:c.5653C>T MANE Select	NP_003997.2:p.Gln1885Ter
ENST00000357033.9:c.5653C>T MANE Select	ENSP00000354923.3:p.Gln1885Ter
NM_000109.3:c.5629C>T	NP_000100.2:p.Gln1877Ter
NM_000109.4:c.5629C>T	NP_000100.3:p.Gln1877Ter
NM_004006.2:c.5653C>T , LRG_199t1:c.5653C>T	NP_003997.1:p.Gln1885Ter
NM_004009.3:c.5641C>T	NP_004000.1:p.Gln1881Ter
NM_004010.3:c.5284C>T	NP_004001.1:p.Gln1762Ter
NM_004011.3:c.1630C>T	NP_004002.2:p.Gln544Ter
NM_004011.4:c.1630C>T	NP_004002.3:p.Gln544Ter
NM_004012.3:c.1621C>T	NP_004003.1:p.Gln541Ter
NM_004012.4:c.1621C>T	NP_004003.2:p.Gln541Ter
ENST00000357033.8:c.5653C>T	ENSP00000354923.3:p.Gln1885Ter
ENST00000358062.7:c.499C>T	ENSP00000350765.3:p.Gln167Ter
ENST00000378677.6:c.5641C>T	ENSP00000367948.2:p.Gln1881Ter
ENST00000488902.5:n.336-126157C>T
ENST00000493412.1:c.310C>T	ENSP00000417725.1:p.Gln104Ter
ENST00000619831.4:c.5641C>T	ENSP00000479270.1:p.Gln1881Ter
ENST00000619831.5:c.1621C>T	ENSP00000479270.2:p.Gln541Ter
ENST00000620040.4:c.5653C>T	ENSP00000478150.1:p.Gln1885Ter
XM_006724468.2:c.5653C>T	XP_006724531.1:p.Gln1885Ter
XM_006724469.2:c.5629C>T	XP_006724532.1:p.Gln1877Ter
XM_006724469.3:c.5629C>T	XP_006724532.1:p.Gln1877Ter
XM_006724470.2:c.5653C>T	XP_006724533.1:p.Gln1885Ter
XM_006724470.3:c.5653C>T	XP_006724533.1:p.Gln1885Ter
XM_006724471.2:c.5653C>T	XP_006724534.1:p.Gln1885Ter
XM_006724472.2:c.5524C>T	XP_006724535.1:p.Gln1842Ter
XM_006724473.2:c.5515C>T	XP_006724536.1:p.Gln1839Ter
XM_006724474.2:c.5653C>T	XP_006724537.1:p.Gln1885Ter
XM_006724474.3:c.5653C>T	XP_006724537.1:p.Gln1885Ter
XM_006724475.2:c.5653C>T	XP_006724538.1:p.Gln1885Ter
XM_011545467.1:c.5530C>T	XP_011543769.1:p.Gln1844Ter
XM_011545468.1:c.5653C>T	XP_011543770.1:p.Gln1885Ter
XM_011545468.2:c.5653C>T	XP_011543770.1:p.Gln1885Ter
XM_011545469.1:c.5653C>T	XP_011543771.1:p.Gln1885Ter
XM_017029328.1:c.5653C>T	XP_016884817.1:p.Gln1885Ter
XM_017029329.1:c.5653C>T	XP_016884818.1:p.Gln1885Ter
XM_017029330.2:c.5653C>T	XP_016884819.1:p.Gln1885Ter