Canonical Allele Identifier: CA412659938

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31875224A>T , CM000685.2:g.31875224A>T	GRCh38
NC_000023.10:g.31893341A>T , CM000685.1:g.31893341A>T	GRCh37
NC_000023.9:g.31803262A>T	NCBI36
NG_012232.1:g.1469386T>A , LRG_199:g.1469386T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004006.3:c.7062T>A MANE Select	NP_003997.2:p.Tyr2354Ter
ENST00000357033.9:c.7062T>A MANE Select	ENSP00000354923.3:p.Tyr2354Ter
NM_000109.3:c.7038T>A	NP_000100.2:p.Tyr2346Ter
NM_000109.4:c.7038T>A	NP_000100.3:p.Tyr2346Ter
NM_004006.2:c.7062T>A , LRG_199t1:c.7062T>A	NP_003997.1:p.Tyr2354Ter
NM_004009.3:c.7050T>A	NP_004000.1:p.Tyr2350Ter
NM_004010.3:c.6693T>A	NP_004001.1:p.Tyr2231Ter
NM_004011.3:c.3039T>A	NP_004002.2:p.Tyr1013Ter
NM_004011.4:c.3039T>A	NP_004002.3:p.Tyr1013Ter
NM_004012.3:c.3030T>A	NP_004003.1:p.Tyr1010Ter
NM_004012.4:c.3030T>A	NP_004003.2:p.Tyr1010Ter
NM_004013.2:c.-319T>A	NP_004004.1:n.-319T>A
NM_004013.3:c.-319T>A	NP_004004.2:n.-319T>A
NM_004020.3:c.-319T>A	NP_004011.2:n.-319T>A
NM_004020.4:c.-319T>A	NP_004011.3:n.-319T>A
NM_004021.2:c.-319T>A	NP_004012.1:n.-319T>A
NM_004021.3:c.-319T>A	NP_004012.2:n.-319T>A
NM_004022.2:c.-319T>A	NP_004013.1:n.-319T>A
NM_004022.3:c.-319T>A	NP_004013.2:n.-319T>A
NM_004023.2:c.-319T>A	NP_004014.1:n.-319T>A
NM_004023.3:c.-319T>A	NP_004014.2:n.-319T>A
ENST00000357033.8:c.7062T>A	ENSP00000354923.3:p.Tyr2354Ter
ENST00000358062.6:c.150T>A	ENSP00000350765.2:p.Tyr50Ter
ENST00000358062.7:c.1908T>A	ENSP00000350765.3:p.Tyr636Ter
ENST00000359836.5:c.-319T>A	ENSP00000352894.1:n.-319T>A
ENST00000378677.6:c.7050T>A	ENSP00000367948.2:p.Tyr2350Ter
ENST00000378707.7:c.-319T>A	ENSP00000367979.3:n.-319T>A
ENST00000474231.5:c.-319T>A	ENSP00000417123.1:n.-319T>A
ENST00000541735.5:c.-319T>A	ENSP00000444119.1:n.-319T>A
ENST00000619831.4:c.7047T>A	ENSP00000479270.1:p.Tyr2349Ter
ENST00000619831.5:c.3030T>A	ENSP00000479270.2:p.Tyr1010Ter
ENST00000620040.4:c.7059T>A	ENSP00000478150.1:p.Tyr2353Ter
ENST00000620040.5:c.-319T>A	ENSP00000478150.2:n.-319T>A
ENST00000680961.1:c.-319T>A	ENSP00000506386.1:n.-319T>A
ENST00000681646.1:n.723T>A
ENST00000682238.1:c.-319T>A	ENSP00000508124.1:n.-319T>A
ENST00000683117.1:n.723T>A
ENST00000683450.1:n.645T>A
ENST00000683851.1:n.723T>A
ENST00000683957.1:n.554T>A
ENST00000684130.1:c.-319T>A	ENSP00000508037.1:n.-319T>A
XM_006724468.2:c.7062T>A	XP_006724531.1:p.Tyr2354Ter
XM_006724469.2:c.7038T>A	XP_006724532.1:p.Tyr2346Ter
XM_006724469.3:c.7038T>A	XP_006724532.1:p.Tyr2346Ter
XM_006724470.2:c.7062T>A	XP_006724533.1:p.Tyr2354Ter
XM_006724470.3:c.7062T>A	XP_006724533.1:p.Tyr2354Ter
XM_006724471.2:c.7062T>A	XP_006724534.1:p.Tyr2354Ter
XM_006724472.2:c.6933T>A	XP_006724535.1:p.Tyr2311Ter
XM_006724473.2:c.6924T>A	XP_006724536.1:p.Tyr2308Ter
XM_006724474.2:c.7062T>A	XP_006724537.1:p.Tyr2354Ter
XM_006724474.3:c.7062T>A	XP_006724537.1:p.Tyr2354Ter
XM_006724475.2:c.7062T>A	XP_006724538.1:p.Tyr2354Ter
XM_011545467.1:c.6939T>A	XP_011543769.1:p.Tyr2313Ter
XM_011545468.1:c.7062T>A	XP_011543770.1:p.Tyr2354Ter
XM_011545468.2:c.7062T>A	XP_011543770.1:p.Tyr2354Ter
XM_017029328.1:c.7062T>A	XP_016884817.1:p.Tyr2354Ter
XM_017029331.1:c.1236T>A	XP_016884820.1:p.Tyr412Ter