Canonical Allele Identifier: CA412658845

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.31792140T>C (hg19) ; chrX:g.31774023T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31774023T>C , CM000685.2:g.31774023T>C	GRCh38
NC_000023.10:g.31792140T>C , CM000685.1:g.31792140T>C	GRCh37
NC_000023.9:g.31702061T>C	NCBI36
NG_012232.1:g.1570587A>G , LRG_199:g.1570587A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.2325A>G	ENSP00000350765.3:p.Ile775Met
ENST00000682238.1:c.99A>G	ENSP00000508124.1:p.Ile33Met
ENST00000683117.1:n.1140A>G
ENST00000683450.1:n.1062A>G
ENST00000683851.1:n.1140A>G
ENST00000683957.1:n.971A>G
ENST00000684130.1:c.99A>G	ENSP00000508037.1:p.Ile33Met
ENST00000357033.9:c.7479A>G MANE Select	ENSP00000354923.3:p.Ile2493Met
ENST00000619831.5:c.3447A>G	ENSP00000479270.2:p.Ile1149Met
ENST00000620040.5:c.99A>G	ENSP00000478150.2:p.Ile33Met
ENST00000680961.1:c.99A>G	ENSP00000506386.1:p.Ile33Met
ENST00000681646.1:n.1140A>G
ENST00000681839.1:c.468A>G	ENSP00000505228.1:p.Ile156Met
ENST00000357033.8:c.7479A>G	ENSP00000354923.3:p.Ile2493Met
ENST00000358062.6:c.567A>G	ENSP00000350765.2:p.Ile189Met
ENST00000359836.5:c.99A>G	ENSP00000352894.1:p.Ile33Met
ENST00000378677.6:c.7467A>G	ENSP00000367948.2:p.Ile2489Met
ENST00000378707.7:c.99A>G	ENSP00000367979.3:p.Ile33Met
ENST00000471779.1:c.236A>G	ENSP00000417075.1:n.236A>G
ENST00000474231.5:c.99A>G	ENSP00000417123.1:p.Ile33Met
ENST00000541735.5:c.99A>G	ENSP00000444119.1:p.Ile33Met
ENST00000619831.4:c.7464A>G	ENSP00000479270.1:p.Ile2488Met
ENST00000620040.4:c.7476A>G	ENSP00000478150.1:p.Ile2492Met
NM_000109.3:c.7455A>G	NP_000100.2:p.Ile2485Met
NM_004006.2:c.7479A>G , LRG_199t1:c.7479A>G	NP_003997.1:p.Ile2493Met
NM_004009.3:c.7467A>G	NP_004000.1:p.Ile2489Met
NM_004010.3:c.7110A>G	NP_004001.1:p.Ile2370Met
NM_004011.3:c.3456A>G	NP_004002.2:p.Ile1152Met
NM_004012.3:c.3447A>G	NP_004003.1:p.Ile1149Met
NM_004013.2:c.99A>G	NP_004004.1:p.Ile33Met
NM_004020.3:c.99A>G	NP_004011.2:p.Ile33Met
NM_004021.2:c.99A>G	NP_004012.1:p.Ile33Met
NM_004022.2:c.99A>G	NP_004013.1:p.Ile33Met
NM_004023.2:c.99A>G	NP_004014.1:p.Ile33Met
XM_006724468.2:c.7479A>G	XP_006724531.1:p.Ile2493Met
XM_006724469.2:c.7455A>G	XP_006724532.1:p.Ile2485Met
XM_006724470.2:c.7479A>G	XP_006724533.1:p.Ile2493Met
XM_006724471.2:c.7479A>G	XP_006724534.1:p.Ile2493Met
XM_006724472.2:c.7350A>G	XP_006724535.1:p.Ile2450Met
XM_006724473.2:c.7341A>G	XP_006724536.1:p.Ile2447Met
XM_006724474.2:c.7479A>G	XP_006724537.1:p.Ile2493Met
XM_006724475.2:c.7479A>G	XP_006724538.1:p.Ile2493Met
XM_011545467.1:c.7356A>G	XP_011543769.1:p.Ile2452Met
XM_011545468.1:c.7479A>G	XP_011543770.1:p.Ile2493Met
XM_006724469.3:c.7455A>G	XP_006724532.1:p.Ile2485Met
XM_006724470.3:c.7479A>G	XP_006724533.1:p.Ile2493Met
XM_006724474.3:c.7479A>G	XP_006724537.1:p.Ile2493Met
XM_011545468.2:c.7479A>G	XP_011543770.1:p.Ile2493Met
XM_017029328.1:c.7479A>G	XP_016884817.1:p.Ile2493Met
XM_017029331.1:c.1653A>G	XP_016884820.1:p.Ile551Met
NM_000109.4:c.7455A>G	NP_000100.3:p.Ile2485Met
NM_004006.3:c.7479A>G MANE Select	NP_003997.2:p.Ile2493Met
NM_004011.4:c.3456A>G	NP_004002.3:p.Ile1152Met
NM_004012.4:c.3447A>G	NP_004003.2:p.Ile1149Met
NM_004021.3:c.99A>G	NP_004012.2:p.Ile33Met
NM_004023.3:c.99A>G	NP_004014.2:p.Ile33Met
NM_004013.3:c.99A>G	NP_004004.2:p.Ile33Met
NM_004020.4:c.99A>G	NP_004011.3:p.Ile33Met
NM_004022.3:c.99A>G	NP_004013.2:p.Ile33Met