Canonical Allele Identifier: CA412658906

Gene: DMD

Linked Data

• dbSNP Id: rs773102625
• gnomAD v3: X-31774052-C-A
• gnomAD v4: X-31774052-C-A
• MyVariant Identifiers: chrX:g.31792169C>A (hg19) ; chrX:g.31774052C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31774052C>A , CM000685.2:g.31774052C>A	GRCh38
NC_000023.10:g.31792169C>A , CM000685.1:g.31792169C>A	GRCh37
NC_000023.9:g.31702090C>A	NCBI36
NG_012232.1:g.1570558G>T , LRG_199:g.1570558G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.2296G>T	ENSP00000350765.3:p.Asp766Tyr
ENST00000682238.1:c.70G>T	ENSP00000508124.1:p.Asp24Tyr
ENST00000683117.1:n.1111G>T
ENST00000683450.1:n.1033G>T
ENST00000683851.1:n.1111G>T
ENST00000683957.1:n.942G>T
ENST00000684130.1:c.70G>T	ENSP00000508037.1:p.Asp24Tyr
ENST00000357033.9:c.7450G>T MANE Select	ENSP00000354923.3:p.Asp2484Tyr
ENST00000619831.5:c.3418G>T	ENSP00000479270.2:p.Asp1140Tyr
ENST00000620040.5:c.70G>T	ENSP00000478150.2:p.Asp24Tyr
ENST00000680961.1:c.70G>T	ENSP00000506386.1:p.Asp24Tyr
ENST00000681646.1:n.1111G>T
ENST00000681839.1:c.439G>T	ENSP00000505228.1:p.Asp147Tyr
ENST00000357033.8:c.7450G>T	ENSP00000354923.3:p.Asp2484Tyr
ENST00000358062.6:c.538G>T	ENSP00000350765.2:p.Asp180Tyr
ENST00000359836.5:c.70G>T	ENSP00000352894.1:p.Asp24Tyr
ENST00000378677.6:c.7438G>T	ENSP00000367948.2:p.Asp2480Tyr
ENST00000378707.7:c.70G>T	ENSP00000367979.3:p.Asp24Tyr
ENST00000471779.1:c.207G>T	ENSP00000417075.1:n.207G>T
ENST00000474231.5:c.70G>T	ENSP00000417123.1:p.Asp24Tyr
ENST00000541735.5:c.70G>T	ENSP00000444119.1:p.Asp24Tyr
ENST00000619831.4:c.7435G>T	ENSP00000479270.1:p.Asp2479Tyr
ENST00000620040.4:c.7447G>T	ENSP00000478150.1:p.Asp2483Tyr
NM_000109.3:c.7426G>T	NP_000100.2:p.Asp2476Tyr
NM_004006.2:c.7450G>T , LRG_199t1:c.7450G>T	NP_003997.1:p.Asp2484Tyr
NM_004009.3:c.7438G>T	NP_004000.1:p.Asp2480Tyr
NM_004010.3:c.7081G>T	NP_004001.1:p.Asp2361Tyr
NM_004011.3:c.3427G>T	NP_004002.2:p.Asp1143Tyr
NM_004012.3:c.3418G>T	NP_004003.1:p.Asp1140Tyr
NM_004013.2:c.70G>T	NP_004004.1:p.Asp24Tyr
NM_004020.3:c.70G>T	NP_004011.2:p.Asp24Tyr
NM_004021.2:c.70G>T	NP_004012.1:p.Asp24Tyr
NM_004022.2:c.70G>T	NP_004013.1:p.Asp24Tyr
NM_004023.2:c.70G>T	NP_004014.1:p.Asp24Tyr
XM_006724468.2:c.7450G>T	XP_006724531.1:p.Asp2484Tyr
XM_006724469.2:c.7426G>T	XP_006724532.1:p.Asp2476Tyr
XM_006724470.2:c.7450G>T	XP_006724533.1:p.Asp2484Tyr
XM_006724471.2:c.7450G>T	XP_006724534.1:p.Asp2484Tyr
XM_006724472.2:c.7321G>T	XP_006724535.1:p.Asp2441Tyr
XM_006724473.2:c.7312G>T	XP_006724536.1:p.Asp2438Tyr
XM_006724474.2:c.7450G>T	XP_006724537.1:p.Asp2484Tyr
XM_006724475.2:c.7450G>T	XP_006724538.1:p.Asp2484Tyr
XM_011545467.1:c.7327G>T	XP_011543769.1:p.Asp2443Tyr
XM_011545468.1:c.7450G>T	XP_011543770.1:p.Asp2484Tyr
XM_006724469.3:c.7426G>T	XP_006724532.1:p.Asp2476Tyr
XM_006724470.3:c.7450G>T	XP_006724533.1:p.Asp2484Tyr
XM_006724474.3:c.7450G>T	XP_006724537.1:p.Asp2484Tyr
XM_011545468.2:c.7450G>T	XP_011543770.1:p.Asp2484Tyr
XM_017029328.1:c.7450G>T	XP_016884817.1:p.Asp2484Tyr
XM_017029331.1:c.1624G>T	XP_016884820.1:p.Asp542Tyr
NM_000109.4:c.7426G>T	NP_000100.3:p.Asp2476Tyr
NM_004006.3:c.7450G>T MANE Select	NP_003997.2:p.Asp2484Tyr
NM_004011.4:c.3427G>T	NP_004002.3:p.Asp1143Tyr
NM_004012.4:c.3418G>T	NP_004003.2:p.Asp1140Tyr
NM_004021.3:c.70G>T	NP_004012.2:p.Asp24Tyr
NM_004023.3:c.70G>T	NP_004014.2:p.Asp24Tyr
NM_004013.3:c.70G>T	NP_004004.2:p.Asp24Tyr
NM_004020.4:c.70G>T	NP_004011.3:p.Asp24Tyr
NM_004022.3:c.70G>T	NP_004013.2:p.Asp24Tyr