Canonical Allele Identifier: CA328529827

Gene: DMD

Linked Data

• ClinVar Variation Id: 594909
• ClinVar RCV Id: RCV000730310 ; RCV001436772
• dbSNP Id: rs969925680
• gnomAD v2: X-32305735-C-T
• gnomAD v3: X-32287618-C-T
• gnomAD v4: X-32287618-C-T
• MyVariant Identifiers: chrX:g.32305735C>T (hg19) ; chrX:g.32287618C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32287618C>T , CM000685.2:g.32287618C>T	GRCh38
NC_000023.10:g.32305735C>T , CM000685.1:g.32305735C>T	GRCh37
NC_000023.9:g.32215656C>T	NCBI36
NG_012232.1:g.1056992G>A , LRG_199:g.1056992G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.1047G>A	ENSP00000350765.3:p.Thr349=
ENST00000357033.9:c.6201G>A MANE Select	ENSP00000354923.3:p.Thr2067=
ENST00000619831.5:c.2169G>A	ENSP00000479270.2:p.Thr723=
ENST00000357033.8:c.6201G>A	ENSP00000354923.3:p.Thr2067=
ENST00000378677.6:c.6189G>A	ENSP00000367948.2:p.Thr2063=
ENST00000488902.5:n.336-70555G>A
ENST00000619831.4:c.6189G>A	ENSP00000479270.1:p.Thr2063=
ENST00000620040.4:c.6201G>A	ENSP00000478150.1:p.Thr2067=
NM_000109.3:c.6177G>A	NP_000100.2:p.Thr2059=
NM_004006.2:c.6201G>A , LRG_199t1:c.6201G>A	NP_003997.1:p.Thr2067=
NM_004009.3:c.6189G>A	NP_004000.1:p.Thr2063=
NM_004010.3:c.5832G>A	NP_004001.1:p.Thr1944=
NM_004011.3:c.2178G>A	NP_004002.2:p.Thr726=
NM_004012.3:c.2169G>A	NP_004003.1:p.Thr723=
XM_006724468.2:c.6201G>A	XP_006724531.1:p.Thr2067=
XM_006724469.2:c.6177G>A	XP_006724532.1:p.Thr2059=
XM_006724470.2:c.6201G>A	XP_006724533.1:p.Thr2067=
XM_006724471.2:c.6201G>A	XP_006724534.1:p.Thr2067=
XM_006724472.2:c.6072G>A	XP_006724535.1:p.Thr2024=
XM_006724473.2:c.6063G>A	XP_006724536.1:p.Thr2021=
XM_006724474.2:c.6201G>A	XP_006724537.1:p.Thr2067=
XM_006724475.2:c.6201G>A	XP_006724538.1:p.Thr2067=
XM_011545467.1:c.6078G>A	XP_011543769.1:p.Thr2026=
XM_011545468.1:c.6201G>A	XP_011543770.1:p.Thr2067=
XM_006724469.3:c.6177G>A	XP_006724532.1:p.Thr2059=
XM_006724470.3:c.6201G>A	XP_006724533.1:p.Thr2067=
XM_006724474.3:c.6201G>A	XP_006724537.1:p.Thr2067=
XM_011545468.2:c.6201G>A	XP_011543770.1:p.Thr2067=
XM_017029328.1:c.6201G>A	XP_016884817.1:p.Thr2067=
XM_017029329.1:c.6201G>A	XP_016884818.1:p.Thr2067=
XM_017029330.2:c.6201G>A	XP_016884819.1:p.Thr2067=
XM_017029331.1:c.375G>A	XP_016884820.1:p.Thr125=
NM_000109.4:c.6177G>A	NP_000100.3:p.Thr2059=
NM_004006.3:c.6201G>A MANE Select	NP_003997.2:p.Thr2067=
NM_004011.4:c.2178G>A	NP_004002.3:p.Thr726=
NM_004012.4:c.2169G>A	NP_004003.2:p.Thr723=