Canonical Allele Identifier: CA10378832

Gene: DMD

Linked Data

• ClinVar Variation Id: 1743717
• ClinVar RCV Id: RCV002340424 ; RCV003096500
• dbSNP Id: rs762250680
• ExAC: X:32383292 G / C
• gnomAD v2: X-32383292-G-C
• gnomAD v4: X-32365175-G-C
• MyVariant Identifiers: chrX:g.32383292G>C (hg19) ; chrX:g.32365175G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32365175G>C , CM000685.2:g.32365175G>C	GRCh38
NC_000023.10:g.32383292G>C , CM000685.1:g.32383292G>C	GRCh37
NC_000023.9:g.32293213G>C	NCBI36
NG_012232.1:g.979435C>G , LRG_199:g.979435C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357033.9:c.4870C>G MANE Select	ENSP00000354923.3:p.Gln1624Glu
ENST00000619831.5:c.838C>G	ENSP00000479270.2:p.Gln280Glu
ENST00000357033.8:c.4870C>G	ENSP00000354923.3:p.Gln1624Glu
ENST00000378677.6:c.4858C>G	ENSP00000367948.2:p.Gln1620Glu
ENST00000420596.5:c.118C>G	ENSP00000399897.1:p.Gln40Glu
ENST00000448370.5:c.94-465C>G	ENSP00000388559.1:n.94-465C>G
ENST00000488902.5:n.336-148112C>G
ENST00000619831.4:c.4858C>G	ENSP00000479270.1:p.Gln1620Glu
ENST00000620040.4:c.4870C>G	ENSP00000478150.1:p.Gln1624Glu
NM_000109.3:c.4846C>G	NP_000100.2:p.Gln1616Glu
NM_004006.2:c.4870C>G , LRG_199t1:c.4870C>G	NP_003997.1:p.Gln1624Glu
NM_004009.3:c.4858C>G	NP_004000.1:p.Gln1620Glu
NM_004010.3:c.4501C>G	NP_004001.1:p.Gln1501Glu
NM_004011.3:c.847C>G	NP_004002.2:p.Gln283Glu
NM_004012.3:c.838C>G	NP_004003.1:p.Gln280Glu
XM_006724468.2:c.4870C>G	XP_006724531.1:p.Gln1624Glu
XM_006724469.2:c.4846C>G	XP_006724532.1:p.Gln1616Glu
XM_006724470.2:c.4870C>G	XP_006724533.1:p.Gln1624Glu
XM_006724471.2:c.4870C>G	XP_006724534.1:p.Gln1624Glu
XM_006724472.2:c.4741C>G	XP_006724535.1:p.Gln1581Glu
XM_006724473.2:c.4870C>G	XP_006724536.1:p.Gln1624Glu
XM_006724474.2:c.4870C>G	XP_006724537.1:p.Gln1624Glu
XM_006724475.2:c.4870C>G	XP_006724538.1:p.Gln1624Glu
XM_011545467.1:c.4870C>G	XP_011543769.1:p.Gln1624Glu
XM_011545468.1:c.4870C>G	XP_011543770.1:p.Gln1624Glu
XM_011545469.1:c.4870C>G	XP_011543771.1:p.Gln1624Glu
XM_006724469.3:c.4846C>G	XP_006724532.1:p.Gln1616Glu
XM_006724470.3:c.4870C>G	XP_006724533.1:p.Gln1624Glu
XM_006724474.3:c.4870C>G	XP_006724537.1:p.Gln1624Glu
XM_011545468.2:c.4870C>G	XP_011543770.1:p.Gln1624Glu
XM_017029328.1:c.4870C>G	XP_016884817.1:p.Gln1624Glu
XM_017029329.1:c.4870C>G	XP_016884818.1:p.Gln1624Glu
XM_017029330.2:c.4870C>G	XP_016884819.1:p.Gln1624Glu
NM_000109.4:c.4846C>G	NP_000100.3:p.Gln1616Glu
NM_004006.3:c.4870C>G MANE Select	NP_003997.2:p.Gln1624Glu
NM_004011.4:c.847C>G	NP_004002.3:p.Gln283Glu
NM_004012.4:c.838C>G	NP_004003.2:p.Gln280Glu