Canonical Allele Identifier: CA412665178

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.32482809A>G (hg19) ; chrX:g.32464692A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32464692A>G , CM000685.2:g.32464692A>G	GRCh38
NC_000023.10:g.32482809A>G , CM000685.1:g.32482809A>G	GRCh37
NC_000023.9:g.32392730A>G	NCBI36
NG_012232.1:g.879918T>C , LRG_199:g.879918T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682899.1:n.3377T>C
ENST00000357033.9:c.3170T>C MANE Select	ENSP00000354923.3:p.Ile1057Thr
ENST00000357033.8:c.3170T>C	ENSP00000354923.3:p.Ile1057Thr
ENST00000378677.6:c.3158T>C	ENSP00000367948.2:p.Ile1053Thr
ENST00000420596.5:c.94-99493T>C	ENSP00000399897.1:n.94-99493T>C
ENST00000448370.5:c.94-99982T>C	ENSP00000388559.1:n.94-99982T>C
ENST00000488902.5:n.336-247629T>C
ENST00000619831.4:c.3158T>C	ENSP00000479270.1:p.Ile1053Thr
ENST00000620040.4:c.3170T>C	ENSP00000478150.1:p.Ile1057Thr
NM_000109.3:c.3146T>C	NP_000100.2:p.Ile1049Thr
NM_004006.2:c.3170T>C , LRG_199t1:c.3170T>C	NP_003997.1:p.Ile1057Thr
NM_004009.3:c.3158T>C	NP_004000.1:p.Ile1053Thr
NM_004010.3:c.2801T>C	NP_004001.1:p.Ile934Thr
XM_006724468.2:c.3170T>C	XP_006724531.1:p.Ile1057Thr
XM_006724469.2:c.3146T>C	XP_006724532.1:p.Ile1049Thr
XM_006724470.2:c.3170T>C	XP_006724533.1:p.Ile1057Thr
XM_006724471.2:c.3170T>C	XP_006724534.1:p.Ile1057Thr
XM_006724472.2:c.3041T>C	XP_006724535.1:p.Ile1014Thr
XM_006724473.2:c.3170T>C	XP_006724536.1:p.Ile1057Thr
XM_006724474.2:c.3170T>C	XP_006724537.1:p.Ile1057Thr
XM_006724475.2:c.3170T>C	XP_006724538.1:p.Ile1057Thr
XM_011545467.1:c.3170T>C	XP_011543769.1:p.Ile1057Thr
XM_011545468.1:c.3170T>C	XP_011543770.1:p.Ile1057Thr
XM_011545469.1:c.3170T>C	XP_011543771.1:p.Ile1057Thr
XM_006724469.3:c.3146T>C	XP_006724532.1:p.Ile1049Thr
XM_006724470.3:c.3170T>C	XP_006724533.1:p.Ile1057Thr
XM_006724474.3:c.3170T>C	XP_006724537.1:p.Ile1057Thr
XM_011545468.2:c.3170T>C	XP_011543770.1:p.Ile1057Thr
XM_017029328.1:c.3170T>C	XP_016884817.1:p.Ile1057Thr
XM_017029329.1:c.3170T>C	XP_016884818.1:p.Ile1057Thr
XM_017029330.2:c.3170T>C	XP_016884819.1:p.Ile1057Thr
NM_000109.4:c.3146T>C	NP_000100.3:p.Ile1049Thr
NM_004006.3:c.3170T>C MANE Select	NP_003997.2:p.Ile1057Thr