Canonical Allele Identifier: CA515715559

Gene: DMD

Linked Data

• ClinVar Variation Id: 1087403
• ClinVar RCV Id: RCV001405484 ; RCV001836396
• dbSNP Id: rs755632126
• gnomAD v4: X-32464685-G-C
• MyVariant Identifiers: chrX:g.32482802G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32464685G>C , CM000685.2:g.32464685G>C	GRCh38
NC_000023.10:g.32482802G>C , CM000685.1:g.32482802G>C	GRCh37
NC_000023.9:g.32392723G>C	NCBI36
NG_012232.1:g.879925C>G , LRG_199:g.879925C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682899.1:n.3384C>G
ENST00000357033.9:c.3177C>G MANE Select	ENSP00000354923.3:p.Thr1059=
ENST00000357033.8:c.3177C>G	ENSP00000354923.3:p.Thr1059=
ENST00000378677.6:c.3165C>G	ENSP00000367948.2:p.Thr1055=
ENST00000420596.5:c.94-99486C>G	ENSP00000399897.1:n.94-99486C>G
ENST00000448370.5:c.94-99975C>G	ENSP00000388559.1:n.94-99975C>G
ENST00000488902.5:n.336-247622C>G
ENST00000619831.4:c.3165C>G	ENSP00000479270.1:p.Thr1055=
ENST00000620040.4:c.3177C>G	ENSP00000478150.1:p.Thr1059=
NM_000109.3:c.3153C>G	NP_000100.2:p.Thr1051=
NM_004006.2:c.3177C>G , LRG_199t1:c.3177C>G	NP_003997.1:p.Thr1059=
NM_004009.3:c.3165C>G	NP_004000.1:p.Thr1055=
NM_004010.3:c.2808C>G	NP_004001.1:p.Thr936=
XM_006724468.2:c.3177C>G	XP_006724531.1:p.Thr1059=
XM_006724469.2:c.3153C>G	XP_006724532.1:p.Thr1051=
XM_006724470.2:c.3177C>G	XP_006724533.1:p.Thr1059=
XM_006724471.2:c.3177C>G	XP_006724534.1:p.Thr1059=
XM_006724472.2:c.3048C>G	XP_006724535.1:p.Thr1016=
XM_006724473.2:c.3177C>G	XP_006724536.1:p.Thr1059=
XM_006724474.2:c.3177C>G	XP_006724537.1:p.Thr1059=
XM_006724475.2:c.3177C>G	XP_006724538.1:p.Thr1059=
XM_011545467.1:c.3177C>G	XP_011543769.1:p.Thr1059=
XM_011545468.1:c.3177C>G	XP_011543770.1:p.Thr1059=
XM_011545469.1:c.3177C>G	XP_011543771.1:p.Thr1059=
XM_006724469.3:c.3153C>G	XP_006724532.1:p.Thr1051=
XM_006724470.3:c.3177C>G	XP_006724533.1:p.Thr1059=
XM_006724474.3:c.3177C>G	XP_006724537.1:p.Thr1059=
XM_011545468.2:c.3177C>G	XP_011543770.1:p.Thr1059=
XM_017029328.1:c.3177C>G	XP_016884817.1:p.Thr1059=
XM_017029329.1:c.3177C>G	XP_016884818.1:p.Thr1059=
XM_017029330.2:c.3177C>G	XP_016884819.1:p.Thr1059=
NM_000109.4:c.3153C>G	NP_000100.3:p.Thr1051=
NM_004006.3:c.3177C>G MANE Select	NP_003997.2:p.Thr1059=