Canonical Allele Identifier: CA267182

Gene: DMD

Linked Data

• ClinVar Variation Id: 94839
• ClinVar RCV Id: RCV000179641 ; RCV000254753 ; RCV001826766
• dbSNP Id: rs398124092
• MyVariant Identifiers: chrX:g.31241188G>A (hg19) ; chrX:g.31223071G>A (hg38)
• PubMed: PMID:19602481 ; PMID:23891399

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31223071G>A , CM000685.2:g.31223071G>A	GRCh38
NC_000023.10:g.31241188G>A , CM000685.1:g.31241188G>A	GRCh37
NC_000023.9:g.31151109G>A	NCBI36
NG_012232.1:g.2121539C>T , LRG_199:g.2121539C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.4183C>T	ENSP00000350765.3:p.Arg1395Ter
ENST00000680162.2:c.133C>T	ENSP00000506634.2:p.Arg45Ter
ENST00000680768.2:c.133C>T	ENSP00000506359.2:p.Arg45Ter
ENST00000681989.1:n.135C>T
ENST00000682238.1:c.1957C>T	ENSP00000508124.1:p.Arg653Ter
ENST00000682322.1:c.133C>T	ENSP00000507690.1:p.Arg45Ter
ENST00000682600.1:c.133C>T	ENSP00000507640.1:p.Arg45Ter
ENST00000682769.1:n.135C>T
ENST00000683509.1:n.854C>T
ENST00000683675.1:n.436C>T
ENST00000683709.1:n.855C>T
ENST00000683957.1:n.2829C>T
ENST00000684130.1:c.1957C>T	ENSP00000508037.1:p.Arg653Ter
ENST00000343523.7:c.1192C>T	ENSP00000340057.4:p.Arg398Ter
ENST00000357033.9:c.9337C>T MANE Select	ENSP00000354923.3:p.Arg3113Ter
ENST00000619831.5:c.5305C>T	ENSP00000479270.2:p.Arg1769Ter
ENST00000620040.5:c.1957C>T	ENSP00000478150.2:p.Arg653Ter
ENST00000679641.1:c.133C>T	ENSP00000506135.1:p.Arg45Ter
ENST00000680162.1:c.10C>T	ENSP00000506634.1:p.Arg4Ter
ENST00000680355.1:c.133C>T	ENSP00000506257.1:p.Arg45Ter
ENST00000680557.1:c.133C>T	ENSP00000505164.1:p.Arg45Ter
ENST00000680768.1:c.76C>T	ENSP00000506359.1:p.Arg26Ter
ENST00000680961.1:c.1957C>T	ENSP00000506386.1:p.Arg653Ter
ENST00000681153.1:c.133C>T	ENSP00000505124.1:p.Arg45Ter
ENST00000681334.1:c.133C>T	ENSP00000506066.1:p.Arg45Ter
ENST00000681646.1:n.2998C>T
ENST00000681654.1:n.267C>T
ENST00000343523.6:c.1150C>T	ENSP00000340057.3:p.Arg384Ter
ENST00000357033.8:c.9337C>T	ENSP00000354923.3:p.Arg3113Ter
ENST00000358062.6:c.2425C>T	ENSP00000350765.2:p.Arg809Ter
ENST00000359836.5:c.1957C>T	ENSP00000352894.1:p.Arg653Ter
ENST00000361471.8:c.133C>T	ENSP00000354464.4:p.Arg45Ter
ENST00000378677.6:c.9325C>T	ENSP00000367948.2:p.Arg3109Ter
ENST00000378680.6:c.133C>T	ENSP00000367951.2:p.Arg45Ter
ENST00000378702.8:c.133C>T	ENSP00000367974.4:p.Arg45Ter
ENST00000378707.7:c.1957C>T	ENSP00000367979.3:p.Arg653Ter
ENST00000378723.7:c.133C>T	ENSP00000367997.3:p.Arg45Ter
ENST00000469142.1:n.356C>T
ENST00000474231.5:c.1957C>T	ENSP00000417123.1:p.Arg653Ter
ENST00000541735.5:c.1957C>T	ENSP00000444119.1:p.Arg653Ter
ENST00000619831.4:c.9322C>T	ENSP00000479270.1:p.Arg3108Ter
ENST00000620040.4:c.9334C>T	ENSP00000478150.1:p.Arg3112Ter
NM_000109.3:c.9313C>T	NP_000100.2:p.Arg3105Ter
NM_004006.2:c.9337C>T , LRG_199t1:c.9337C>T	NP_003997.1:p.Arg3113Ter
NM_004009.3:c.9325C>T	NP_004000.1:p.Arg3109Ter
NM_004010.3:c.8968C>T	NP_004001.1:p.Arg2990Ter
NM_004011.3:c.5314C>T	NP_004002.2:p.Arg1772Ter
NM_004012.3:c.5305C>T	NP_004003.1:p.Arg1769Ter
NM_004013.2:c.1957C>T	NP_004004.1:p.Arg653Ter
NM_004014.2:c.1150C>T	NP_004005.1:p.Arg384Ter
NM_004015.2:c.133C>T	NP_004006.1:p.Arg45Ter
NM_004016.2:c.133C>T	NP_004007.1:p.Arg45Ter
NM_004017.2:c.133C>T	NP_004008.1:p.Arg45Ter
NM_004018.2:c.133C>T	NP_004009.1:p.Arg45Ter
NM_004019.2:c.133C>T	NP_004010.1:p.Arg45Ter
NM_004020.3:c.1957C>T	NP_004011.2:p.Arg653Ter
NM_004021.2:c.1957C>T	NP_004012.1:p.Arg653Ter
NM_004022.2:c.1957C>T	NP_004013.1:p.Arg653Ter
NM_004023.2:c.1957C>T	NP_004014.1:p.Arg653Ter
XM_006724468.2:c.9337C>T	XP_006724531.1:p.Arg3113Ter
XM_006724469.2:c.9313C>T	XP_006724532.1:p.Arg3105Ter
XM_006724470.2:c.9337C>T	XP_006724533.1:p.Arg3113Ter
XM_006724471.2:c.9337C>T	XP_006724534.1:p.Arg3113Ter
XM_006724472.2:c.9208C>T	XP_006724535.1:p.Arg3070Ter
XM_006724473.2:c.9199C>T	XP_006724536.1:p.Arg3067Ter
XM_006724474.2:c.9337C>T	XP_006724537.1:p.Arg3113Ter
XM_006724475.2:c.9337C>T	XP_006724538.1:p.Arg3113Ter
XM_011545467.1:c.9214C>T	XP_011543769.1:p.Arg3072Ter
XM_011545468.1:c.9337C>T	XP_011543770.1:p.Arg3113Ter
XM_006724469.3:c.9313C>T	XP_006724532.1:p.Arg3105Ter
XM_006724470.3:c.9337C>T	XP_006724533.1:p.Arg3113Ter
XM_006724474.3:c.9337C>T	XP_006724537.1:p.Arg3113Ter
XM_011545468.2:c.9337C>T	XP_011543770.1:p.Arg3113Ter
XM_017029328.1:c.9337C>T	XP_016884817.1:p.Arg3113Ter
XM_017029331.1:c.3511C>T	XP_016884820.1:p.Arg1171Ter
NM_000109.4:c.9313C>T	NP_000100.3:p.Arg3105Ter
NM_004006.3:c.9337C>T MANE Select	NP_003997.2:p.Arg3113Ter
NM_004011.4:c.5314C>T	NP_004002.3:p.Arg1772Ter
NM_004012.4:c.5305C>T	NP_004003.2:p.Arg1769Ter
NM_004015.3:c.133C>T	NP_004006.1:p.Arg45Ter
NM_004016.3:c.133C>T	NP_004007.1:p.Arg45Ter
NM_004017.3:c.133C>T	NP_004008.1:p.Arg45Ter
NM_004018.3:c.133C>T	NP_004009.1:p.Arg45Ter
NM_004019.3:c.133C>T	NP_004010.1:p.Arg45Ter
NM_004021.3:c.1957C>T	NP_004012.2:p.Arg653Ter
NM_004023.3:c.1957C>T	NP_004014.2:p.Arg653Ter
NM_004013.3:c.1957C>T	NP_004004.2:p.Arg653Ter
NM_004014.3:c.1150C>T	NP_004005.2:p.Arg384Ter
NM_004020.4:c.1957C>T	NP_004011.3:p.Arg653Ter
NM_004022.3:c.1957C>T	NP_004013.2:p.Arg653Ter