Canonical Allele Identifier: CA412652521

Gene: DMD

Linked Data

• COSMIC: COSM1120145 ; COSM1120147 ; COSM1120149 ; COSM1120150 ; COSM1599220 ; COSM1599221
• MyVariant Identifiers: chrX:g.31279112G>T (hg19) ; chrX:g.31260995G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31260995G>T , CM000685.2:g.31260995G>T	GRCh38
NC_000023.10:g.31279112G>T , CM000685.1:g.31279112G>T	GRCh37
NC_000023.9:g.31189033G>T	NCBI36
NG_012232.1:g.2083615C>A , LRG_199:g.2083615C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.4092C>A	ENSP00000350765.3:p.Cys1364Ter
ENST00000680162.2:c.42C>A	ENSP00000506634.2:p.Cys14Ter
ENST00000680768.2:c.42C>A	ENSP00000506359.2:p.Cys14Ter
ENST00000682238.1:c.1866C>A	ENSP00000508124.1:p.Cys622Ter
ENST00000682322.1:c.42C>A	ENSP00000507690.1:p.Cys14Ter
ENST00000682600.1:c.42C>A	ENSP00000507640.1:p.Cys14Ter
ENST00000683509.1:n.763C>A
ENST00000683675.1:n.345C>A
ENST00000683709.1:n.764C>A
ENST00000683957.1:n.2738C>A
ENST00000684130.1:c.1866C>A	ENSP00000508037.1:p.Cys622Ter
ENST00000343523.7:c.1101C>A	ENSP00000340057.4:p.Cys367Ter
ENST00000357033.9:c.9246C>A MANE Select	ENSP00000354923.3:p.Cys3082Ter
ENST00000619831.5:c.5214C>A	ENSP00000479270.2:p.Cys1738Ter
ENST00000620040.5:c.1866C>A	ENSP00000478150.2:p.Cys622Ter
ENST00000679641.1:c.42C>A	ENSP00000506135.1:p.Cys14Ter
ENST00000680216.1:c.22C>A
ENST00000680355.1:c.42C>A	ENSP00000506257.1:p.Cys14Ter
ENST00000680557.1:c.42C>A	ENSP00000505164.1:p.Cys14Ter
ENST00000680768.1:c.-16C>A	ENSP00000506359.1:n.-16C>A
ENST00000680961.1:c.1866C>A	ENSP00000506386.1:p.Cys622Ter
ENST00000681153.1:c.42C>A	ENSP00000505124.1:p.Cys14Ter
ENST00000681334.1:c.42C>A	ENSP00000506066.1:p.Cys14Ter
ENST00000681646.1:n.2907C>A
ENST00000681654.1:n.176C>A
ENST00000681870.1:c.42C>A	ENSP00000506709.1:p.Cys14Ter
ENST00000343523.6:c.1059C>A	ENSP00000340057.3:p.Cys353Ter
ENST00000357033.8:c.9246C>A	ENSP00000354923.3:p.Cys3082Ter
ENST00000358062.6:c.2334C>A	ENSP00000350765.2:p.Cys778Ter
ENST00000359836.5:c.1866C>A	ENSP00000352894.1:p.Cys622Ter
ENST00000361471.8:c.42C>A	ENSP00000354464.4:p.Cys14Ter
ENST00000378677.6:c.9234C>A	ENSP00000367948.2:p.Cys3078Ter
ENST00000378680.6:c.42C>A	ENSP00000367951.2:p.Cys14Ter
ENST00000378702.8:c.42C>A	ENSP00000367974.4:p.Cys14Ter
ENST00000378707.7:c.1866C>A	ENSP00000367979.3:p.Cys622Ter
ENST00000378723.7:c.42C>A	ENSP00000367997.3:p.Cys14Ter
ENST00000469142.1:n.265C>A
ENST00000474231.5:c.1866C>A	ENSP00000417123.1:p.Cys622Ter
ENST00000541735.5:c.1866C>A	ENSP00000444119.1:p.Cys622Ter
ENST00000619831.4:c.9231C>A	ENSP00000479270.1:p.Cys3077Ter
ENST00000620040.4:c.9243C>A	ENSP00000478150.1:p.Cys3081Ter
NM_000109.3:c.9222C>A	NP_000100.2:p.Cys3074Ter
NM_004006.2:c.9246C>A , LRG_199t1:c.9246C>A	NP_003997.1:p.Cys3082Ter
NM_004009.3:c.9234C>A	NP_004000.1:p.Cys3078Ter
NM_004010.3:c.8877C>A	NP_004001.1:p.Cys2959Ter
NM_004011.3:c.5223C>A	NP_004002.2:p.Cys1741Ter
NM_004012.3:c.5214C>A	NP_004003.1:p.Cys1738Ter
NM_004013.2:c.1866C>A	NP_004004.1:p.Cys622Ter
NM_004014.2:c.1059C>A	NP_004005.1:p.Cys353Ter
NM_004015.2:c.42C>A	NP_004006.1:p.Cys14Ter
NM_004016.2:c.42C>A	NP_004007.1:p.Cys14Ter
NM_004017.2:c.42C>A	NP_004008.1:p.Cys14Ter
NM_004018.2:c.42C>A	NP_004009.1:p.Cys14Ter
NM_004019.2:c.42C>A	NP_004010.1:p.Cys14Ter
NM_004020.3:c.1866C>A	NP_004011.2:p.Cys622Ter
NM_004021.2:c.1866C>A	NP_004012.1:p.Cys622Ter
NM_004022.2:c.1866C>A	NP_004013.1:p.Cys622Ter
NM_004023.2:c.1866C>A	NP_004014.1:p.Cys622Ter
XM_006724468.2:c.9246C>A	XP_006724531.1:p.Cys3082Ter
XM_006724469.2:c.9222C>A	XP_006724532.1:p.Cys3074Ter
XM_006724470.2:c.9246C>A	XP_006724533.1:p.Cys3082Ter
XM_006724471.2:c.9246C>A	XP_006724534.1:p.Cys3082Ter
XM_006724472.2:c.9117C>A	XP_006724535.1:p.Cys3039Ter
XM_006724473.2:c.9108C>A	XP_006724536.1:p.Cys3036Ter
XM_006724474.2:c.9246C>A	XP_006724537.1:p.Cys3082Ter
XM_006724475.2:c.9246C>A	XP_006724538.1:p.Cys3082Ter
XM_011545467.1:c.9123C>A	XP_011543769.1:p.Cys3041Ter
XM_011545468.1:c.9246C>A	XP_011543770.1:p.Cys3082Ter
XM_006724469.3:c.9222C>A	XP_006724532.1:p.Cys3074Ter
XM_006724470.3:c.9246C>A	XP_006724533.1:p.Cys3082Ter
XM_006724474.3:c.9246C>A	XP_006724537.1:p.Cys3082Ter
XM_011545468.2:c.9246C>A	XP_011543770.1:p.Cys3082Ter
XM_017029328.1:c.9246C>A	XP_016884817.1:p.Cys3082Ter
XM_017029331.1:c.3420C>A	XP_016884820.1:p.Cys1140Ter
NM_000109.4:c.9222C>A	NP_000100.3:p.Cys3074Ter
NM_004006.3:c.9246C>A MANE Select	NP_003997.2:p.Cys3082Ter
NM_004011.4:c.5223C>A	NP_004002.3:p.Cys1741Ter
NM_004012.4:c.5214C>A	NP_004003.2:p.Cys1738Ter
NM_004015.3:c.42C>A	NP_004006.1:p.Cys14Ter
NM_004016.3:c.42C>A	NP_004007.1:p.Cys14Ter
NM_004017.3:c.42C>A	NP_004008.1:p.Cys14Ter
NM_004018.3:c.42C>A	NP_004009.1:p.Cys14Ter
NM_004019.3:c.42C>A	NP_004010.1:p.Cys14Ter
NM_004021.3:c.1866C>A	NP_004012.2:p.Cys622Ter
NM_004023.3:c.1866C>A	NP_004014.2:p.Cys622Ter
NM_004013.3:c.1866C>A	NP_004004.2:p.Cys622Ter
NM_004014.3:c.1059C>A	NP_004005.2:p.Cys353Ter
NM_004020.4:c.1866C>A	NP_004011.3:p.Cys622Ter
NM_004022.3:c.1866C>A	NP_004013.2:p.Cys622Ter