Canonical Allele Identifier: CA10606837

Gene: DMD

Linked Data

• ClinVar Variation Id: 290597
• ClinVar RCV Id: RCV000299536 ; RCV001473755 ; RCV002429238
• dbSNP Id: rs886044500
• MyVariant Identifiers: chrX:g.31645835G>A (hg19) ; chrX:g.31627718G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31627718G>A , CM000685.2:g.31627718G>A	GRCh38
NC_000023.10:g.31645835G>A , CM000685.1:g.31645835G>A	GRCh37
NC_000023.9:g.31555756G>A	NCBI36
NG_012232.1:g.1716892C>T , LRG_199:g.1716892C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.3018C>T	ENSP00000350765.3:p.Leu1006=
ENST00000682238.1:c.792C>T	ENSP00000508124.1:p.Leu264=
ENST00000683450.1:n.1637C>T
ENST00000683851.1:n.1833C>T
ENST00000683957.1:n.1664C>T
ENST00000684130.1:c.792C>T	ENSP00000508037.1:p.Leu264=
ENST00000357033.9:c.8172C>T MANE Select	ENSP00000354923.3:p.Leu2724=
ENST00000619831.5:c.4140C>T	ENSP00000479270.2:p.Leu1380=
ENST00000620040.5:c.792C>T	ENSP00000478150.2:p.Leu264=
ENST00000680961.1:c.792C>T	ENSP00000506386.1:p.Leu264=
ENST00000681646.1:n.1833C>T
ENST00000357033.8:c.8172C>T	ENSP00000354923.3:p.Leu2724=
ENST00000358062.6:c.1260C>T	ENSP00000350765.2:p.Leu420=
ENST00000359836.5:c.792C>T	ENSP00000352894.1:p.Leu264=
ENST00000378677.6:c.8160C>T	ENSP00000367948.2:p.Leu2720=
ENST00000378707.7:c.792C>T	ENSP00000367979.3:p.Leu264=
ENST00000474231.5:c.792C>T	ENSP00000417123.1:p.Leu264=
ENST00000541735.5:c.792C>T	ENSP00000444119.1:p.Leu264=
ENST00000619831.4:c.8157C>T	ENSP00000479270.1:p.Leu2719=
ENST00000620040.4:c.8169C>T	ENSP00000478150.1:p.Leu2723=
NM_000109.3:c.8148C>T	NP_000100.2:p.Leu2716=
NM_004006.2:c.8172C>T , LRG_199t1:c.8172C>T	NP_003997.1:p.Leu2724=
NM_004009.3:c.8160C>T	NP_004000.1:p.Leu2720=
NM_004010.3:c.7803C>T	NP_004001.1:p.Leu2601=
NM_004011.3:c.4149C>T	NP_004002.2:p.Leu1383=
NM_004012.3:c.4140C>T	NP_004003.1:p.Leu1380=
NM_004013.2:c.792C>T	NP_004004.1:p.Leu264=
NM_004020.3:c.792C>T	NP_004011.2:p.Leu264=
NM_004021.2:c.792C>T	NP_004012.1:p.Leu264=
NM_004022.2:c.792C>T	NP_004013.1:p.Leu264=
NM_004023.2:c.792C>T	NP_004014.1:p.Leu264=
XM_006724468.2:c.8172C>T	XP_006724531.1:p.Leu2724=
XM_006724469.2:c.8148C>T	XP_006724532.1:p.Leu2716=
XM_006724470.2:c.8172C>T	XP_006724533.1:p.Leu2724=
XM_006724471.2:c.8172C>T	XP_006724534.1:p.Leu2724=
XM_006724472.2:c.8043C>T	XP_006724535.1:p.Leu2681=
XM_006724473.2:c.8034C>T	XP_006724536.1:p.Leu2678=
XM_006724474.2:c.8172C>T	XP_006724537.1:p.Leu2724=
XM_006724475.2:c.8172C>T	XP_006724538.1:p.Leu2724=
XM_011545467.1:c.8049C>T	XP_011543769.1:p.Leu2683=
XM_011545468.1:c.8172C>T	XP_011543770.1:p.Leu2724=
XM_006724469.3:c.8148C>T	XP_006724532.1:p.Leu2716=
XM_006724470.3:c.8172C>T	XP_006724533.1:p.Leu2724=
XM_006724474.3:c.8172C>T	XP_006724537.1:p.Leu2724=
XM_011545468.2:c.8172C>T	XP_011543770.1:p.Leu2724=
XM_017029328.1:c.8172C>T	XP_016884817.1:p.Leu2724=
XM_017029331.1:c.2346C>T	XP_016884820.1:p.Leu782=
NM_000109.4:c.8148C>T	NP_000100.3:p.Leu2716=
NM_004006.3:c.8172C>T MANE Select	NP_003997.2:p.Leu2724=
NM_004011.4:c.4149C>T	NP_004002.3:p.Leu1383=
NM_004012.4:c.4140C>T	NP_004003.2:p.Leu1380=
NM_004021.3:c.792C>T	NP_004012.2:p.Leu264=
NM_004023.3:c.792C>T	NP_004014.2:p.Leu264=
NM_004013.3:c.792C>T	NP_004004.2:p.Leu264=
NM_004020.4:c.792C>T	NP_004011.3:p.Leu264=
NM_004022.3:c.792C>T	NP_004013.2:p.Leu264=