Canonical Allele Identifier: CA412659615

Gene: DMD

Linked Data

• ClinVar Variation Id: 498985
• ClinVar RCV Id: RCV000591973 ; RCV002368009 ; RCV003325968
• dbSNP Id: rs1557038061
• MyVariant Identifiers: chrX:g.31986526G>A (hg19) ; chrX:g.31968409G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31968409G>A , CM000685.2:g.31968409G>A	GRCh38
NC_000023.10:g.31986526G>A , CM000685.1:g.31986526G>A	GRCh37
NC_000023.9:g.31896447G>A	NCBI36
NG_012232.1:g.1376201C>T , LRG_199:g.1376201C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.1390C>T	ENSP00000350765.3:p.Gln464Ter
ENST00000682135.1:n.205C>T
ENST00000682183.1:n.205C>T
ENST00000682238.1:c.-837C>T	ENSP00000508124.1:n.-837C>T
ENST00000683117.1:n.205C>T
ENST00000683450.1:n.205C>T
ENST00000683851.1:n.205C>T
ENST00000684130.1:c.-837C>T	ENSP00000508037.1:n.-837C>T
ENST00000357033.9:c.6544C>T MANE Select	ENSP00000354923.3:p.Gln2182Ter
ENST00000619831.5:c.2512C>T	ENSP00000479270.2:p.Gln838Ter
ENST00000620040.5:c.-837C>T	ENSP00000478150.2:n.-837C>T
ENST00000680961.1:c.-837C>T	ENSP00000506386.1:n.-837C>T
ENST00000681646.1:n.205C>T
ENST00000357033.8:c.6544C>T	ENSP00000354923.3:p.Gln2182Ter
ENST00000359836.5:c.-837C>T	ENSP00000352894.1:n.-837C>T
ENST00000378677.6:c.6532C>T	ENSP00000367948.2:p.Gln2178Ter
ENST00000378707.7:c.-837C>T	ENSP00000367979.3:n.-837C>T
ENST00000474231.5:c.-837C>T	ENSP00000417123.1:n.-837C>T
ENST00000488902.5:n.589C>T
ENST00000541735.5:c.-837C>T	ENSP00000444119.1:n.-837C>T
ENST00000619831.4:c.6529C>T	ENSP00000479270.1:p.Gln2177Ter
ENST00000620040.4:c.6541C>T	ENSP00000478150.1:p.Gln2181Ter
NM_000109.3:c.6520C>T	NP_000100.2:p.Gln2174Ter
NM_004006.2:c.6544C>T , LRG_199t1:c.6544C>T	NP_003997.1:p.Gln2182Ter
NM_004009.3:c.6532C>T	NP_004000.1:p.Gln2178Ter
NM_004010.3:c.6175C>T	NP_004001.1:p.Gln2059Ter
NM_004011.3:c.2521C>T	NP_004002.2:p.Gln841Ter
NM_004012.3:c.2512C>T	NP_004003.1:p.Gln838Ter
NM_004013.2:c.-837C>T	NP_004004.1:n.-837C>T
NM_004020.3:c.-837C>T	NP_004011.2:n.-837C>T
NM_004021.2:c.-837C>T	NP_004012.1:n.-837C>T
NM_004022.2:c.-837C>T	NP_004013.1:n.-837C>T
NM_004023.2:c.-837C>T	NP_004014.1:n.-837C>T
XM_006724468.2:c.6544C>T	XP_006724531.1:p.Gln2182Ter
XM_006724469.2:c.6520C>T	XP_006724532.1:p.Gln2174Ter
XM_006724470.2:c.6544C>T	XP_006724533.1:p.Gln2182Ter
XM_006724471.2:c.6544C>T	XP_006724534.1:p.Gln2182Ter
XM_006724472.2:c.6415C>T	XP_006724535.1:p.Gln2139Ter
XM_006724473.2:c.6406C>T	XP_006724536.1:p.Gln2136Ter
XM_006724474.2:c.6544C>T	XP_006724537.1:p.Gln2182Ter
XM_006724475.2:c.6544C>T	XP_006724538.1:p.Gln2182Ter
XM_011545467.1:c.6421C>T	XP_011543769.1:p.Gln2141Ter
XM_011545468.1:c.6544C>T	XP_011543770.1:p.Gln2182Ter
XM_006724469.3:c.6520C>T	XP_006724532.1:p.Gln2174Ter
XM_006724470.3:c.6544C>T	XP_006724533.1:p.Gln2182Ter
XM_006724474.3:c.6544C>T	XP_006724537.1:p.Gln2182Ter
XM_011545468.2:c.6544C>T	XP_011543770.1:p.Gln2182Ter
XM_017029328.1:c.6544C>T	XP_016884817.1:p.Gln2182Ter
XM_017029331.1:c.718C>T	XP_016884820.1:p.Gln240Ter
NM_000109.4:c.6520C>T	NP_000100.3:p.Gln2174Ter
NM_004006.3:c.6544C>T MANE Select	NP_003997.2:p.Gln2182Ter
NM_004011.4:c.2521C>T	NP_004002.3:p.Gln841Ter
NM_004012.4:c.2512C>T	NP_004003.2:p.Gln838Ter
NM_004021.3:c.-837C>T	NP_004012.2:n.-837C>T
NM_004023.3:c.-837C>T	NP_004014.2:n.-837C>T
NM_004013.3:c.-837C>T	NP_004004.2:n.-837C>T
NM_004020.4:c.-837C>T	NP_004011.3:n.-837C>T
NM_004022.3:c.-837C>T	NP_004013.2:n.-837C>T