Canonical Allele Identifier: CA412665568

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.32361261C>G (hg19) ; chrX:g.32343144C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32343144C>G , CM000685.2:g.32343144C>G	GRCh38
NC_000023.10:g.32361261C>G , CM000685.1:g.32361261C>G	GRCh37
NC_000023.9:g.32271182C>G	NCBI36
NG_012232.1:g.1001466G>C , LRG_199:g.1001466G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.575G>C	ENSP00000350765.3:p.Arg192Thr
ENST00000357033.9:c.5729G>C MANE Select	ENSP00000354923.3:p.Arg1910Thr
ENST00000619831.5:c.1697G>C	ENSP00000479270.2:p.Arg566Thr
ENST00000357033.8:c.5729G>C	ENSP00000354923.3:p.Arg1910Thr
ENST00000378677.6:c.5717G>C	ENSP00000367948.2:p.Arg1906Thr
ENST00000488902.5:n.336-126081G>C
ENST00000493412.1:c.386G>C	ENSP00000417725.1:p.Arg129Thr
ENST00000619831.4:c.5717G>C	ENSP00000479270.1:p.Arg1906Thr
ENST00000620040.4:c.5729G>C	ENSP00000478150.1:p.Arg1910Thr
NM_000109.3:c.5705G>C	NP_000100.2:p.Arg1902Thr
NM_004006.2:c.5729G>C , LRG_199t1:c.5729G>C	NP_003997.1:p.Arg1910Thr
NM_004009.3:c.5717G>C	NP_004000.1:p.Arg1906Thr
NM_004010.3:c.5360G>C	NP_004001.1:p.Arg1787Thr
NM_004011.3:c.1706G>C	NP_004002.2:p.Arg569Thr
NM_004012.3:c.1697G>C	NP_004003.1:p.Arg566Thr
XM_006724468.2:c.5729G>C	XP_006724531.1:p.Arg1910Thr
XM_006724469.2:c.5705G>C	XP_006724532.1:p.Arg1902Thr
XM_006724470.2:c.5729G>C	XP_006724533.1:p.Arg1910Thr
XM_006724471.2:c.5729G>C	XP_006724534.1:p.Arg1910Thr
XM_006724472.2:c.5600G>C	XP_006724535.1:p.Arg1867Thr
XM_006724473.2:c.5591G>C	XP_006724536.1:p.Arg1864Thr
XM_006724474.2:c.5729G>C	XP_006724537.1:p.Arg1910Thr
XM_006724475.2:c.5729G>C	XP_006724538.1:p.Arg1910Thr
XM_011545467.1:c.5606G>C	XP_011543769.1:p.Arg1869Thr
XM_011545468.1:c.5729G>C	XP_011543770.1:p.Arg1910Thr
XM_011545469.1:c.5729G>C	XP_011543771.1:p.Arg1910Thr
XM_006724469.3:c.5705G>C	XP_006724532.1:p.Arg1902Thr
XM_006724470.3:c.5729G>C	XP_006724533.1:p.Arg1910Thr
XM_006724474.3:c.5729G>C	XP_006724537.1:p.Arg1910Thr
XM_011545468.2:c.5729G>C	XP_011543770.1:p.Arg1910Thr
XM_017029328.1:c.5729G>C	XP_016884817.1:p.Arg1910Thr
XM_017029329.1:c.5729G>C	XP_016884818.1:p.Arg1910Thr
XM_017029330.2:c.5729G>C	XP_016884819.1:p.Arg1910Thr
NM_000109.4:c.5705G>C	NP_000100.3:p.Arg1902Thr
NM_004006.3:c.5729G>C MANE Select	NP_003997.2:p.Arg1910Thr
NM_004011.4:c.1706G>C	NP_004002.3:p.Arg569Thr
NM_004012.4:c.1697G>C	NP_004003.2:p.Arg566Thr