Canonical Allele Identifier: CA341073

Gene: DMD

Linked Data

• ClinVar Variation Id: 11266
• ClinVar RCV Id: RCV000012017
• dbSNP Id: rs128626253
• MyVariant Identifiers: chrX:g.31792217C>A (hg19) ; chrX:g.31774100C>A (hg38)
• PubMed: PMID:1301174

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31774100C>A , CM000685.2:g.31774100C>A	GRCh38
NC_000023.10:g.31792217C>A , CM000685.1:g.31792217C>A	GRCh37
NC_000023.9:g.31702138C>A	NCBI36
NG_012232.1:g.1570510G>T , LRG_199:g.1570510G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000358062.7:c.2248G>T	ENSP00000350765.3:p.Glu750Ter
ENST00000682238.1:c.22G>T	ENSP00000508124.1:p.Glu8Ter
ENST00000683117.1:n.1063G>T
ENST00000683450.1:n.985G>T
ENST00000683851.1:n.1063G>T
ENST00000683957.1:n.894G>T
ENST00000684130.1:c.22G>T	ENSP00000508037.1:p.Glu8Ter
ENST00000357033.9:c.7402G>T MANE Select	ENSP00000354923.3:p.Glu2468Ter
ENST00000619831.5:c.3370G>T	ENSP00000479270.2:p.Glu1124Ter
ENST00000620040.5:c.22G>T	ENSP00000478150.2:p.Glu8Ter
ENST00000680961.1:c.22G>T	ENSP00000506386.1:p.Glu8Ter
ENST00000681646.1:n.1063G>T
ENST00000681839.1:c.391G>T	ENSP00000505228.1:p.Glu131Ter
ENST00000357033.8:c.7402G>T	ENSP00000354923.3:p.Glu2468Ter
ENST00000358062.6:c.490G>T	ENSP00000350765.2:p.Glu164Ter
ENST00000359836.5:c.22G>T	ENSP00000352894.1:p.Glu8Ter
ENST00000378677.6:c.7390G>T	ENSP00000367948.2:p.Glu2464Ter
ENST00000378707.7:c.22G>T	ENSP00000367979.3:p.Glu8Ter
ENST00000471779.1:c.159G>T	ENSP00000417075.1:n.159G>T
ENST00000474231.5:c.22G>T	ENSP00000417123.1:p.Glu8Ter
ENST00000541735.5:c.22G>T	ENSP00000444119.1:p.Glu8Ter
ENST00000619831.4:c.7387G>T	ENSP00000479270.1:p.Glu2463Ter
ENST00000620040.4:c.7399G>T	ENSP00000478150.1:p.Glu2467Ter
NM_000109.3:c.7378G>T	NP_000100.2:p.Glu2460Ter
NM_004006.2:c.7402G>T , LRG_199t1:c.7402G>T	NP_003997.1:p.Glu2468Ter
NM_004009.3:c.7390G>T	NP_004000.1:p.Glu2464Ter
NM_004010.3:c.7033G>T	NP_004001.1:p.Glu2345Ter
NM_004011.3:c.3379G>T	NP_004002.2:p.Glu1127Ter
NM_004012.3:c.3370G>T	NP_004003.1:p.Glu1124Ter
NM_004013.2:c.22G>T	NP_004004.1:p.Glu8Ter
NM_004020.3:c.22G>T	NP_004011.2:p.Glu8Ter
NM_004021.2:c.22G>T	NP_004012.1:p.Glu8Ter
NM_004022.2:c.22G>T	NP_004013.1:p.Glu8Ter
NM_004023.2:c.22G>T	NP_004014.1:p.Glu8Ter
XM_006724468.2:c.7402G>T	XP_006724531.1:p.Glu2468Ter
XM_006724469.2:c.7378G>T	XP_006724532.1:p.Glu2460Ter
XM_006724470.2:c.7402G>T	XP_006724533.1:p.Glu2468Ter
XM_006724471.2:c.7402G>T	XP_006724534.1:p.Glu2468Ter
XM_006724472.2:c.7273G>T	XP_006724535.1:p.Glu2425Ter
XM_006724473.2:c.7264G>T	XP_006724536.1:p.Glu2422Ter
XM_006724474.2:c.7402G>T	XP_006724537.1:p.Glu2468Ter
XM_006724475.2:c.7402G>T	XP_006724538.1:p.Glu2468Ter
XM_011545467.1:c.7279G>T	XP_011543769.1:p.Glu2427Ter
XM_011545468.1:c.7402G>T	XP_011543770.1:p.Glu2468Ter
XM_006724469.3:c.7378G>T	XP_006724532.1:p.Glu2460Ter
XM_006724470.3:c.7402G>T	XP_006724533.1:p.Glu2468Ter
XM_006724474.3:c.7402G>T	XP_006724537.1:p.Glu2468Ter
XM_011545468.2:c.7402G>T	XP_011543770.1:p.Glu2468Ter
XM_017029328.1:c.7402G>T	XP_016884817.1:p.Glu2468Ter
XM_017029331.1:c.1576G>T	XP_016884820.1:p.Glu526Ter
NM_000109.4:c.7378G>T	NP_000100.3:p.Glu2460Ter
NM_004006.3:c.7402G>T MANE Select	NP_003997.2:p.Glu2468Ter
NM_004011.4:c.3379G>T	NP_004002.3:p.Glu1127Ter
NM_004012.4:c.3370G>T	NP_004003.2:p.Glu1124Ter
NM_004021.3:c.22G>T	NP_004012.2:p.Glu8Ter
NM_004023.3:c.22G>T	NP_004014.2:p.Glu8Ter
NM_004013.3:c.22G>T	NP_004004.2:p.Glu8Ter
NM_004020.4:c.22G>T	NP_004011.3:p.Glu8Ter
NM_004022.3:c.22G>T	NP_004013.2:p.Glu8Ter