Canonical Allele Identifier: CA412657090

Gene: DMD

Linked Data

• ClinVar Variation Id: 2994898
• ClinVar RCV Id: RCV003858521
• dbSNP Id: rs1219165101
• gnomAD v2: X-31645809-T-C
• gnomAD v3: X-31627692-T-C
• gnomAD v4: X-31627692-T-C
• MyVariant Identifiers: chrX:g.31645809T>C (hg19) ; chrX:g.31627692T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31627692T>C , CM000685.2:g.31627692T>C	GRCh38
NC_000023.10:g.31645809T>C , CM000685.1:g.31645809T>C	GRCh37
NC_000023.9:g.31555730T>C	NCBI36
NG_012232.1:g.1716918A>G , LRG_199:g.1716918A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.3044A>G	ENSP00000350765.3:p.Glu1015Gly
ENST00000682238.1:c.818A>G	ENSP00000508124.1:p.Glu273Gly
ENST00000683450.1:n.1663A>G
ENST00000683851.1:n.1859A>G
ENST00000683957.1:n.1690A>G
ENST00000684130.1:c.818A>G	ENSP00000508037.1:p.Glu273Gly
ENST00000357033.9:c.8198A>G MANE Select	ENSP00000354923.3:p.Glu2733Gly
ENST00000619831.5:c.4166A>G	ENSP00000479270.2:p.Glu1389Gly
ENST00000620040.5:c.818A>G	ENSP00000478150.2:p.Glu273Gly
ENST00000680961.1:c.818A>G	ENSP00000506386.1:p.Glu273Gly
ENST00000681646.1:n.1859A>G
ENST00000357033.8:c.8198A>G	ENSP00000354923.3:p.Glu2733Gly
ENST00000358062.6:c.1286A>G	ENSP00000350765.2:p.Glu429Gly
ENST00000359836.5:c.818A>G	ENSP00000352894.1:p.Glu273Gly
ENST00000378677.6:c.8186A>G	ENSP00000367948.2:p.Glu2729Gly
ENST00000378707.7:c.818A>G	ENSP00000367979.3:p.Glu273Gly
ENST00000474231.5:c.818A>G	ENSP00000417123.1:p.Glu273Gly
ENST00000541735.5:c.818A>G	ENSP00000444119.1:p.Glu273Gly
ENST00000619831.4:c.8183A>G	ENSP00000479270.1:p.Glu2728Gly
ENST00000620040.4:c.8195A>G	ENSP00000478150.1:p.Glu2732Gly
NM_000109.3:c.8174A>G	NP_000100.2:p.Glu2725Gly
NM_004006.2:c.8198A>G , LRG_199t1:c.8198A>G	NP_003997.1:p.Glu2733Gly
NM_004009.3:c.8186A>G	NP_004000.1:p.Glu2729Gly
NM_004010.3:c.7829A>G	NP_004001.1:p.Glu2610Gly
NM_004011.3:c.4175A>G	NP_004002.2:p.Glu1392Gly
NM_004012.3:c.4166A>G	NP_004003.1:p.Glu1389Gly
NM_004013.2:c.818A>G	NP_004004.1:p.Glu273Gly
NM_004020.3:c.818A>G	NP_004011.2:p.Glu273Gly
NM_004021.2:c.818A>G	NP_004012.1:p.Glu273Gly
NM_004022.2:c.818A>G	NP_004013.1:p.Glu273Gly
NM_004023.2:c.818A>G	NP_004014.1:p.Glu273Gly
XM_006724468.2:c.8198A>G	XP_006724531.1:p.Glu2733Gly
XM_006724469.2:c.8174A>G	XP_006724532.1:p.Glu2725Gly
XM_006724470.2:c.8198A>G	XP_006724533.1:p.Glu2733Gly
XM_006724471.2:c.8198A>G	XP_006724534.1:p.Glu2733Gly
XM_006724472.2:c.8069A>G	XP_006724535.1:p.Glu2690Gly
XM_006724473.2:c.8060A>G	XP_006724536.1:p.Glu2687Gly
XM_006724474.2:c.8198A>G	XP_006724537.1:p.Glu2733Gly
XM_006724475.2:c.8198A>G	XP_006724538.1:p.Glu2733Gly
XM_011545467.1:c.8075A>G	XP_011543769.1:p.Glu2692Gly
XM_011545468.1:c.8198A>G	XP_011543770.1:p.Glu2733Gly
XM_006724469.3:c.8174A>G	XP_006724532.1:p.Glu2725Gly
XM_006724470.3:c.8198A>G	XP_006724533.1:p.Glu2733Gly
XM_006724474.3:c.8198A>G	XP_006724537.1:p.Glu2733Gly
XM_011545468.2:c.8198A>G	XP_011543770.1:p.Glu2733Gly
XM_017029328.1:c.8198A>G	XP_016884817.1:p.Glu2733Gly
XM_017029331.1:c.2372A>G	XP_016884820.1:p.Glu791Gly
NM_000109.4:c.8174A>G	NP_000100.3:p.Glu2725Gly
NM_004006.3:c.8198A>G MANE Select	NP_003997.2:p.Glu2733Gly
NM_004011.4:c.4175A>G	NP_004002.3:p.Glu1392Gly
NM_004012.4:c.4166A>G	NP_004003.2:p.Glu1389Gly
NM_004021.3:c.818A>G	NP_004012.2:p.Glu273Gly
NM_004023.3:c.818A>G	NP_004014.2:p.Glu273Gly
NM_004013.3:c.818A>G	NP_004004.2:p.Glu273Gly
NM_004020.4:c.818A>G	NP_004011.3:p.Glu273Gly
NM_004022.3:c.818A>G	NP_004013.2:p.Glu273Gly