Canonical Allele Identifier: CA412672075

Gene: DMD

Linked Data

• gnomAD v4: X-32365103-A-T
• MyVariant Identifiers: chrX:g.32383220A>T (hg19) ; chrX:g.32365103A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32365103A>T , CM000685.2:g.32365103A>T	GRCh38
NC_000023.10:g.32383220A>T , CM000685.1:g.32383220A>T	GRCh37
NC_000023.9:g.32293141A>T	NCBI36
NG_012232.1:g.979507T>A , LRG_199:g.979507T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357033.9:c.4942T>A MANE Select	ENSP00000354923.3:p.Leu1648Met
ENST00000619831.5:c.910T>A	ENSP00000479270.2:p.Leu304Met
ENST00000357033.8:c.4942T>A	ENSP00000354923.3:p.Leu1648Met
ENST00000378677.6:c.4930T>A	ENSP00000367948.2:p.Leu1644Met
ENST00000420596.5:c.190T>A	ENSP00000399897.1:p.Leu64Met
ENST00000448370.5:c.94-393T>A	ENSP00000388559.1:n.94-393T>A
ENST00000488902.5:n.336-148040T>A
ENST00000619831.4:c.4930T>A	ENSP00000479270.1:p.Leu1644Met
ENST00000620040.4:c.4942T>A	ENSP00000478150.1:p.Leu1648Met
NM_000109.3:c.4918T>A	NP_000100.2:p.Leu1640Met
NM_004006.2:c.4942T>A , LRG_199t1:c.4942T>A	NP_003997.1:p.Leu1648Met
NM_004009.3:c.4930T>A	NP_004000.1:p.Leu1644Met
NM_004010.3:c.4573T>A	NP_004001.1:p.Leu1525Met
NM_004011.3:c.919T>A	NP_004002.2:p.Leu307Met
NM_004012.3:c.910T>A	NP_004003.1:p.Leu304Met
XM_006724468.2:c.4942T>A	XP_006724531.1:p.Leu1648Met
XM_006724469.2:c.4918T>A	XP_006724532.1:p.Leu1640Met
XM_006724470.2:c.4942T>A	XP_006724533.1:p.Leu1648Met
XM_006724471.2:c.4942T>A	XP_006724534.1:p.Leu1648Met
XM_006724472.2:c.4813T>A	XP_006724535.1:p.Leu1605Met
XM_006724473.2:c.4942T>A	XP_006724536.1:p.Leu1648Met
XM_006724474.2:c.4942T>A	XP_006724537.1:p.Leu1648Met
XM_006724475.2:c.4942T>A	XP_006724538.1:p.Leu1648Met
XM_011545467.1:c.4942T>A	XP_011543769.1:p.Leu1648Met
XM_011545468.1:c.4942T>A	XP_011543770.1:p.Leu1648Met
XM_011545469.1:c.4942T>A	XP_011543771.1:p.Leu1648Met
XM_006724469.3:c.4918T>A	XP_006724532.1:p.Leu1640Met
XM_006724470.3:c.4942T>A	XP_006724533.1:p.Leu1648Met
XM_006724474.3:c.4942T>A	XP_006724537.1:p.Leu1648Met
XM_011545468.2:c.4942T>A	XP_011543770.1:p.Leu1648Met
XM_017029328.1:c.4942T>A	XP_016884817.1:p.Leu1648Met
XM_017029329.1:c.4942T>A	XP_016884818.1:p.Leu1648Met
XM_017029330.2:c.4942T>A	XP_016884819.1:p.Leu1648Met
NM_000109.4:c.4918T>A	NP_000100.3:p.Leu1640Met
NM_004006.3:c.4942T>A MANE Select	NP_003997.2:p.Leu1648Met
NM_004011.4:c.919T>A	NP_004002.3:p.Leu307Met
NM_004012.4:c.910T>A	NP_004003.2:p.Leu304Met