Canonical Allele Identifier: CA515866112

Gene: DMD

Linked Data

• ClinVar Variation Id: 1138514
• ClinVar RCV Id: RCV001474885
• dbSNP Id: rs2148807117
• MyVariant Identifiers: chrX:g.32834692C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32816575C>T , CM000685.2:g.32816575C>T	GRCh38
NC_000023.10:g.32834692C>T , CM000685.1:g.32834692C>T	GRCh37
NC_000023.9:g.32744613C>T	NCBI36
NG_012232.1:g.528035G>A , LRG_199:g.528035G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682071.1:c.54G>A	ENSP00000508133.1:p.Leu18=
ENST00000682437.1:n.747G>A
ENST00000682870.1:n.608G>A
ENST00000682899.1:n.630G>A
ENST00000682924.1:c.423G>A	ENSP00000508187.1:p.Leu141=
ENST00000683309.1:n.607G>A
ENST00000683658.1:n.768G>A
ENST00000683985.1:n.630G>A
ENST00000684056.1:n.607G>A
ENST00000684165.1:n.630G>A
ENST00000684237.1:c.423G>A	ENSP00000507277.1:p.Leu141=
ENST00000684292.1:n.630G>A
ENST00000684660.1:n.608G>A
ENST00000288447.9:c.399G>A	ENSP00000288447.4:p.Leu133=
ENST00000357033.9:c.423G>A MANE Select	ENSP00000354923.3:p.Leu141=
ENST00000288447.8:c.399G>A	ENSP00000288447.4:p.Leu133=
ENST00000357033.8:c.423G>A	ENSP00000354923.3:p.Leu141=
ENST00000378677.6:c.411G>A	ENSP00000367948.2:p.Leu137=
ENST00000420596.5:c.93+203564G>A	ENSP00000399897.1:n.93+203564G>A
ENST00000447523.1:c.246+6720G>A	ENSP00000395904.1:n.246+6720G>A
ENST00000448370.5:c.93+203564G>A	ENSP00000388559.1:n.93+203564G>A
ENST00000488902.5:n.335+203564G>A
ENST00000619831.4:c.411G>A	ENSP00000479270.1:p.Leu137=
ENST00000620040.4:c.423G>A	ENSP00000478150.1:p.Leu141=
NM_000109.3:c.399G>A	NP_000100.2:p.Leu133=
NM_004006.2:c.423G>A , LRG_199t1:c.423G>A	NP_003997.1:p.Leu141=
NM_004009.3:c.411G>A	NP_004000.1:p.Leu137=
NM_004010.3:c.54G>A	NP_004001.1:p.Leu18=
XM_006724468.2:c.423G>A	XP_006724531.1:p.Leu141=
XM_006724469.2:c.399G>A	XP_006724532.1:p.Leu133=
XM_006724470.2:c.423G>A	XP_006724533.1:p.Leu141=
XM_006724471.2:c.423G>A	XP_006724534.1:p.Leu141=
XM_006724472.2:c.423G>A	XP_006724535.1:p.Leu141=
XM_006724473.2:c.423G>A	XP_006724536.1:p.Leu141=
XM_006724474.2:c.423G>A	XP_006724537.1:p.Leu141=
XM_006724475.2:c.423G>A	XP_006724538.1:p.Leu141=
XM_011545467.1:c.423G>A	XP_011543769.1:p.Leu141=
XM_011545468.1:c.423G>A	XP_011543770.1:p.Leu141=
XM_011545469.1:c.423G>A	XP_011543771.1:p.Leu141=
XM_006724469.3:c.399G>A	XP_006724532.1:p.Leu133=
XM_006724470.3:c.423G>A	XP_006724533.1:p.Leu141=
XM_006724474.3:c.423G>A	XP_006724537.1:p.Leu141=
XM_011545468.2:c.423G>A	XP_011543770.1:p.Leu141=
XM_017029328.1:c.423G>A	XP_016884817.1:p.Leu141=
XM_017029329.1:c.423G>A	XP_016884818.1:p.Leu141=
XM_017029330.2:c.423G>A	XP_016884819.1:p.Leu141=
NM_000109.4:c.399G>A	NP_000100.3:p.Leu133=
NM_004006.3:c.423G>A MANE Select	NP_003997.2:p.Leu141=