Canonical Allele Identifier: CA412669896

Gene: DMD

Linked Data

• ClinVar Variation Id: 828072
• ClinVar RCV Id: RCV001027923 ; RCV001243442
• dbSNP Id: rs1603630432
• gnomAD v4: X-32310200-T-A
• MyVariant Identifiers: chrX:g.32328317T>A (hg19) ; chrX:g.32310200T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32310200T>A , CM000685.2:g.32310200T>A	GRCh38
NC_000023.10:g.32328317T>A , CM000685.1:g.32328317T>A	GRCh37
NC_000023.9:g.32238238T>A	NCBI36
NG_012232.1:g.1034410A>T , LRG_199:g.1034410A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.845A>T	ENSP00000350765.3:p.Tyr282Phe
ENST00000357033.9:c.5999A>T MANE Select	ENSP00000354923.3:p.Tyr2000Phe
ENST00000619831.5:c.1967A>T	ENSP00000479270.2:p.Tyr656Phe
ENST00000357033.8:c.5999A>T	ENSP00000354923.3:p.Tyr2000Phe
ENST00000378677.6:c.5987A>T	ENSP00000367948.2:p.Tyr1996Phe
ENST00000488902.5:n.336-93137A>T
ENST00000619831.4:c.5987A>T	ENSP00000479270.1:p.Tyr1996Phe
ENST00000620040.4:c.5999A>T	ENSP00000478150.1:p.Tyr2000Phe
NM_000109.3:c.5975A>T	NP_000100.2:p.Tyr1992Phe
NM_004006.2:c.5999A>T , LRG_199t1:c.5999A>T	NP_003997.1:p.Tyr2000Phe
NM_004009.3:c.5987A>T	NP_004000.1:p.Tyr1996Phe
NM_004010.3:c.5630A>T	NP_004001.1:p.Tyr1877Phe
NM_004011.3:c.1976A>T	NP_004002.2:p.Tyr659Phe
NM_004012.3:c.1967A>T	NP_004003.1:p.Tyr656Phe
XM_006724468.2:c.5999A>T	XP_006724531.1:p.Tyr2000Phe
XM_006724469.2:c.5975A>T	XP_006724532.1:p.Tyr1992Phe
XM_006724470.2:c.5999A>T	XP_006724533.1:p.Tyr2000Phe
XM_006724471.2:c.5999A>T	XP_006724534.1:p.Tyr2000Phe
XM_006724472.2:c.5870A>T	XP_006724535.1:p.Tyr1957Phe
XM_006724473.2:c.5861A>T	XP_006724536.1:p.Tyr1954Phe
XM_006724474.2:c.5999A>T	XP_006724537.1:p.Tyr2000Phe
XM_006724475.2:c.5999A>T	XP_006724538.1:p.Tyr2000Phe
XM_011545467.1:c.5876A>T	XP_011543769.1:p.Tyr1959Phe
XM_011545468.1:c.5999A>T	XP_011543770.1:p.Tyr2000Phe
XM_006724469.3:c.5975A>T	XP_006724532.1:p.Tyr1992Phe
XM_006724470.3:c.5999A>T	XP_006724533.1:p.Tyr2000Phe
XM_006724474.3:c.5999A>T	XP_006724537.1:p.Tyr2000Phe
XM_011545468.2:c.5999A>T	XP_011543770.1:p.Tyr2000Phe
XM_017029328.1:c.5999A>T	XP_016884817.1:p.Tyr2000Phe
XM_017029329.1:c.5999A>T	XP_016884818.1:p.Tyr2000Phe
XM_017029330.2:c.5999A>T	XP_016884819.1:p.Tyr2000Phe
XM_017029331.1:c.173A>T	XP_016884820.1:p.Tyr58Phe
NM_000109.4:c.5975A>T	NP_000100.3:p.Tyr1992Phe
NM_004006.3:c.5999A>T MANE Select	NP_003997.2:p.Tyr2000Phe
NM_004011.4:c.1976A>T	NP_004002.3:p.Tyr659Phe
NM_004012.4:c.1967A>T	NP_004003.2:p.Tyr656Phe