Canonical Allele Identifier: CA515860937

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.32305807A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32287690A>G , CM000685.2:g.32287690A>G	GRCh38
NC_000023.10:g.32305807A>G , CM000685.1:g.32305807A>G	GRCh37
NC_000023.9:g.32215728A>G	NCBI36
NG_012232.1:g.1056920T>C , LRG_199:g.1056920T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000358062.7:c.975T>C	ENSP00000350765.3:p.Asp325=
ENST00000357033.9:c.6129T>C MANE Select	ENSP00000354923.3:p.Asp2043=
ENST00000619831.5:c.2097T>C	ENSP00000479270.2:p.Asp699=
ENST00000357033.8:c.6129T>C	ENSP00000354923.3:p.Asp2043=
ENST00000378677.6:c.6117T>C	ENSP00000367948.2:p.Asp2039=
ENST00000488902.5:n.336-70627T>C
ENST00000619831.4:c.6117T>C	ENSP00000479270.1:p.Asp2039=
ENST00000620040.4:c.6129T>C	ENSP00000478150.1:p.Asp2043=
NM_000109.3:c.6105T>C	NP_000100.2:p.Asp2035=
NM_004006.2:c.6129T>C , LRG_199t1:c.6129T>C	NP_003997.1:p.Asp2043=
NM_004009.3:c.6117T>C	NP_004000.1:p.Asp2039=
NM_004010.3:c.5760T>C	NP_004001.1:p.Asp1920=
NM_004011.3:c.2106T>C	NP_004002.2:p.Asp702=
NM_004012.3:c.2097T>C	NP_004003.1:p.Asp699=
XM_006724468.2:c.6129T>C	XP_006724531.1:p.Asp2043=
XM_006724469.2:c.6105T>C	XP_006724532.1:p.Asp2035=
XM_006724470.2:c.6129T>C	XP_006724533.1:p.Asp2043=
XM_006724471.2:c.6129T>C	XP_006724534.1:p.Asp2043=
XM_006724472.2:c.6000T>C	XP_006724535.1:p.Asp2000=
XM_006724473.2:c.5991T>C	XP_006724536.1:p.Asp1997=
XM_006724474.2:c.6129T>C	XP_006724537.1:p.Asp2043=
XM_006724475.2:c.6129T>C	XP_006724538.1:p.Asp2043=
XM_011545467.1:c.6006T>C	XP_011543769.1:p.Asp2002=
XM_011545468.1:c.6129T>C	XP_011543770.1:p.Asp2043=
XM_006724469.3:c.6105T>C	XP_006724532.1:p.Asp2035=
XM_006724470.3:c.6129T>C	XP_006724533.1:p.Asp2043=
XM_006724474.3:c.6129T>C	XP_006724537.1:p.Asp2043=
XM_011545468.2:c.6129T>C	XP_011543770.1:p.Asp2043=
XM_017029328.1:c.6129T>C	XP_016884817.1:p.Asp2043=
XM_017029329.1:c.6129T>C	XP_016884818.1:p.Asp2043=
XM_017029330.2:c.6129T>C	XP_016884819.1:p.Asp2043=
XM_017029331.1:c.303T>C	XP_016884820.1:p.Asp101=
NM_000109.4:c.6105T>C	NP_000100.3:p.Asp2035=
NM_004006.3:c.6129T>C MANE Select	NP_003997.2:p.Asp2043=
NM_004011.4:c.2106T>C	NP_004002.3:p.Asp702=
NM_004012.4:c.2097T>C	NP_004003.2:p.Asp699=