Canonical Allele Identifier: CA2573158587

Gene: DMD

Linked Data

• ClinVar Variation Id: 1653225
• ClinVar RCV Id: RCV002160960
• dbSNP Id: rs2147602930

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32699105A>G , CM000685.2:g.32699105A>G	GRCh38
NC_000023.10:g.32717222A>G , CM000685.1:g.32717222A>G	GRCh37
NC_000023.9:g.32627143A>G	NCBI36
NG_012232.1:g.645505T>C , LRG_199:g.645505T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682071.1:c.462+7T>C	ENSP00000508133.1:n.462+7T>C
ENST00000682870.1:n.1016+7T>C
ENST00000682899.1:n.1038+7T>C
ENST00000682924.1:c.831+7T>C	ENSP00000508187.1:n.831+7T>C
ENST00000683985.1:n.1038+7T>C
ENST00000684165.1:n.1038+7T>C
ENST00000684237.1:c.831+7T>C	ENSP00000507277.1:n.831+7T>C
ENST00000684292.1:n.1038+7T>C
ENST00000684660.1:n.1023T>C
ENST00000288447.9:c.807+7T>C	ENSP00000288447.4:n.807+7T>C
ENST00000357033.9:c.831+7T>C MANE Select	ENSP00000354923.3:n.831+7T>C
ENST00000288447.8:c.807+7T>C	ENSP00000288447.4:n.807+7T>C
ENST00000357033.8:c.831+7T>C	ENSP00000354923.3:n.831+7T>C
ENST00000378677.6:c.819+7T>C	ENSP00000367948.2:n.819+7T>C
ENST00000420596.5:c.93+321034T>C	ENSP00000399897.1:n.93+321034T>C
ENST00000447523.1:c.246+124190T>C	ENSP00000395904.1:n.246+124190T>C
ENST00000448370.5:c.93+321034T>C	ENSP00000388559.1:n.93+321034T>C
ENST00000480751.1:n.86+117363T>C
ENST00000488902.5:n.335+321034T>C
ENST00000619831.4:c.819+7T>C	ENSP00000479270.1:n.819+7T>C
ENST00000620040.4:c.831+7T>C	ENSP00000478150.1:n.831+7T>C
NM_000109.3:c.807+7T>C	NP_000100.2:n.807+7T>C
NM_004006.2:c.831+7T>C , LRG_199t1:c.831+7T>C	NP_003997.1:n.831+7T>C
NM_004009.3:c.819+7T>C	NP_004000.1:n.819+7T>C
NM_004010.3:c.462+7T>C	NP_004001.1:n.462+7T>C
XM_006724468.2:c.831+7T>C	XP_006724531.1:n.831+7T>C
XM_006724469.2:c.807+7T>C	XP_006724532.1:n.807+7T>C
XM_006724470.2:c.831+7T>C	XP_006724533.1:n.831+7T>C
XM_006724471.2:c.831+7T>C	XP_006724534.1:n.831+7T>C
XM_006724472.2:c.831+7T>C	XP_006724535.1:n.831+7T>C
XM_006724473.2:c.831+7T>C	XP_006724536.1:n.831+7T>C
XM_006724474.2:c.831+7T>C	XP_006724537.1:n.831+7T>C
XM_006724475.2:c.831+7T>C	XP_006724538.1:n.831+7T>C
XM_011545467.1:c.831+7T>C	XP_011543769.1:n.831+7T>C
XM_011545468.1:c.831+7T>C	XP_011543770.1:n.831+7T>C
XM_011545469.1:c.831+7T>C	XP_011543771.1:n.831+7T>C
XM_006724469.3:c.807+7T>C	XP_006724532.1:n.807+7T>C
XM_006724470.3:c.831+7T>C	XP_006724533.1:n.831+7T>C
XM_006724474.3:c.831+7T>C	XP_006724537.1:n.831+7T>C
XM_011545468.2:c.831+7T>C	XP_011543770.1:n.831+7T>C
XM_017029328.1:c.831+7T>C	XP_016884817.1:n.831+7T>C
XM_017029329.1:c.831+7T>C	XP_016884818.1:n.831+7T>C
XM_017029330.2:c.831+7T>C	XP_016884819.1:n.831+7T>C
NM_000109.4:c.807+7T>C	NP_000100.3:n.807+7T>C
NM_004006.3:c.831+7T>C MANE Select	NP_003997.2:n.831+7T>C