Canonical Allele Identifier: CA515859437

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.31792302A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31774185A>C , CM000685.2:g.31774185A>C	GRCh38
NC_000023.10:g.31792302A>C , CM000685.1:g.31792302A>C	GRCh37
NC_000023.9:g.31702223A>C	NCBI36
NG_012232.1:g.1570425T>G , LRG_199:g.1570425T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.2163T>G	ENSP00000350765.3:p.Thr721=
ENST00000682238.1:c.-64T>G	ENSP00000508124.1:n.-64T>G
ENST00000683117.1:n.978T>G
ENST00000683450.1:n.900T>G
ENST00000683851.1:n.978T>G
ENST00000683957.1:n.809T>G
ENST00000684130.1:c.-64T>G	ENSP00000508037.1:n.-64T>G
ENST00000357033.9:c.7317T>G MANE Select	ENSP00000354923.3:p.Thr2439=
ENST00000619831.5:c.3285T>G	ENSP00000479270.2:p.Thr1095=
ENST00000620040.5:c.-64T>G	ENSP00000478150.2:n.-64T>G
ENST00000680961.1:c.-64T>G	ENSP00000506386.1:n.-64T>G
ENST00000681646.1:n.978T>G
ENST00000681839.1:c.306T>G	ENSP00000505228.1:p.Thr102=
ENST00000357033.8:c.7317T>G	ENSP00000354923.3:p.Thr2439=
ENST00000358062.6:c.405T>G	ENSP00000350765.2:p.Thr135=
ENST00000359836.5:c.-64T>G	ENSP00000352894.1:n.-64T>G
ENST00000378677.6:c.7305T>G	ENSP00000367948.2:p.Thr2435=
ENST00000378707.7:c.-64T>G	ENSP00000367979.3:n.-64T>G
ENST00000471779.1:c.74T>G	ENSP00000417075.1:p.Leu25Arg
ENST00000474231.5:c.-64T>G	ENSP00000417123.1:n.-64T>G
ENST00000541735.5:c.-64T>G	ENSP00000444119.1:n.-64T>G
ENST00000619831.4:c.7302T>G	ENSP00000479270.1:p.Thr2434=
ENST00000620040.4:c.7314T>G	ENSP00000478150.1:p.Thr2438=
NM_000109.3:c.7293T>G	NP_000100.2:p.Thr2431=
NM_004006.2:c.7317T>G , LRG_199t1:c.7317T>G	NP_003997.1:p.Thr2439=
NM_004009.3:c.7305T>G	NP_004000.1:p.Thr2435=
NM_004010.3:c.6948T>G	NP_004001.1:p.Thr2316=
NM_004011.3:c.3294T>G	NP_004002.2:p.Thr1098=
NM_004012.3:c.3285T>G	NP_004003.1:p.Thr1095=
NM_004013.2:c.-64T>G	NP_004004.1:n.-64T>G
NM_004020.3:c.-64T>G	NP_004011.2:n.-64T>G
NM_004021.2:c.-64T>G	NP_004012.1:n.-64T>G
NM_004022.2:c.-64T>G	NP_004013.1:n.-64T>G
NM_004023.2:c.-64T>G	NP_004014.1:n.-64T>G
XM_006724468.2:c.7317T>G	XP_006724531.1:p.Thr2439=
XM_006724469.2:c.7293T>G	XP_006724532.1:p.Thr2431=
XM_006724470.2:c.7317T>G	XP_006724533.1:p.Thr2439=
XM_006724471.2:c.7317T>G	XP_006724534.1:p.Thr2439=
XM_006724472.2:c.7188T>G	XP_006724535.1:p.Thr2396=
XM_006724473.2:c.7179T>G	XP_006724536.1:p.Thr2393=
XM_006724474.2:c.7317T>G	XP_006724537.1:p.Thr2439=
XM_006724475.2:c.7317T>G	XP_006724538.1:p.Thr2439=
XM_011545467.1:c.7194T>G	XP_011543769.1:p.Thr2398=
XM_011545468.1:c.7317T>G	XP_011543770.1:p.Thr2439=
XM_006724469.3:c.7293T>G	XP_006724532.1:p.Thr2431=
XM_006724470.3:c.7317T>G	XP_006724533.1:p.Thr2439=
XM_006724474.3:c.7317T>G	XP_006724537.1:p.Thr2439=
XM_011545468.2:c.7317T>G	XP_011543770.1:p.Thr2439=
XM_017029328.1:c.7317T>G	XP_016884817.1:p.Thr2439=
XM_017029331.1:c.1491T>G	XP_016884820.1:p.Thr497=
NM_000109.4:c.7293T>G	NP_000100.3:p.Thr2431=
NM_004006.3:c.7317T>G MANE Select	NP_003997.2:p.Thr2439=
NM_004011.4:c.3294T>G	NP_004002.3:p.Thr1098=
NM_004012.4:c.3285T>G	NP_004003.2:p.Thr1095=
NM_004021.3:c.-64T>G	NP_004012.2:n.-64T>G
NM_004023.3:c.-64T>G	NP_004014.2:n.-64T>G
NM_004013.3:c.-64T>G	NP_004004.2:n.-64T>G
NM_004020.4:c.-64T>G	NP_004011.3:n.-64T>G
NM_004022.3:c.-64T>G	NP_004013.2:n.-64T>G