Canonical Allele Identifier: CA412665154

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.32482803G>C (hg19) ; chrX:g.32464686G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32464686G>C , CM000685.2:g.32464686G>C	GRCh38
NC_000023.10:g.32482803G>C , CM000685.1:g.32482803G>C	GRCh37
NC_000023.9:g.32392724G>C	NCBI36
NG_012232.1:g.879924C>G , LRG_199:g.879924C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682899.1:n.3383C>G
ENST00000357033.9:c.3176C>G MANE Select	ENSP00000354923.3:p.Thr1059Ser
ENST00000357033.8:c.3176C>G	ENSP00000354923.3:p.Thr1059Ser
ENST00000378677.6:c.3164C>G	ENSP00000367948.2:p.Thr1055Ser
ENST00000420596.5:c.94-99487C>G	ENSP00000399897.1:n.94-99487C>G
ENST00000448370.5:c.94-99976C>G	ENSP00000388559.1:n.94-99976C>G
ENST00000488902.5:n.336-247623C>G
ENST00000619831.4:c.3164C>G	ENSP00000479270.1:p.Thr1055Ser
ENST00000620040.4:c.3176C>G	ENSP00000478150.1:p.Thr1059Ser
NM_000109.3:c.3152C>G	NP_000100.2:p.Thr1051Ser
NM_004006.2:c.3176C>G , LRG_199t1:c.3176C>G	NP_003997.1:p.Thr1059Ser
NM_004009.3:c.3164C>G	NP_004000.1:p.Thr1055Ser
NM_004010.3:c.2807C>G	NP_004001.1:p.Thr936Ser
XM_006724468.2:c.3176C>G	XP_006724531.1:p.Thr1059Ser
XM_006724469.2:c.3152C>G	XP_006724532.1:p.Thr1051Ser
XM_006724470.2:c.3176C>G	XP_006724533.1:p.Thr1059Ser
XM_006724471.2:c.3176C>G	XP_006724534.1:p.Thr1059Ser
XM_006724472.2:c.3047C>G	XP_006724535.1:p.Thr1016Ser
XM_006724473.2:c.3176C>G	XP_006724536.1:p.Thr1059Ser
XM_006724474.2:c.3176C>G	XP_006724537.1:p.Thr1059Ser
XM_006724475.2:c.3176C>G	XP_006724538.1:p.Thr1059Ser
XM_011545467.1:c.3176C>G	XP_011543769.1:p.Thr1059Ser
XM_011545468.1:c.3176C>G	XP_011543770.1:p.Thr1059Ser
XM_011545469.1:c.3176C>G	XP_011543771.1:p.Thr1059Ser
XM_006724469.3:c.3152C>G	XP_006724532.1:p.Thr1051Ser
XM_006724470.3:c.3176C>G	XP_006724533.1:p.Thr1059Ser
XM_006724474.3:c.3176C>G	XP_006724537.1:p.Thr1059Ser
XM_011545468.2:c.3176C>G	XP_011543770.1:p.Thr1059Ser
XM_017029328.1:c.3176C>G	XP_016884817.1:p.Thr1059Ser
XM_017029329.1:c.3176C>G	XP_016884818.1:p.Thr1059Ser
XM_017029330.2:c.3176C>G	XP_016884819.1:p.Thr1059Ser
NM_000109.4:c.3152C>G	NP_000100.3:p.Thr1051Ser
NM_004006.3:c.3176C>G MANE Select	NP_003997.2:p.Thr1059Ser