Canonical Allele Identifier: CA412660829

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.32662254T>G (hg19) ; chrX:g.32644137T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32644137T>G , CM000685.2:g.32644137T>G	GRCh38
NC_000023.10:g.32662254T>G , CM000685.1:g.32662254T>G	GRCh37
NC_000023.9:g.32572175T>G	NCBI36
NG_012232.1:g.700473A>C , LRG_199:g.700473A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682071.1:c.957A>C	ENSP00000508133.1:p.Gln319His
ENST00000682899.1:n.1533A>C
ENST00000682924.1:c.1326A>C	ENSP00000508187.1:p.Gln442His
ENST00000683985.1:n.1533A>C
ENST00000684165.1:n.1533A>C
ENST00000684237.1:c.1197A>C	ENSP00000507277.1:p.Gln399His
ENST00000684292.1:n.1533A>C
ENST00000288447.9:c.1302A>C	ENSP00000288447.4:p.Gln434His
ENST00000357033.9:c.1326A>C MANE Select	ENSP00000354923.3:p.Gln442His
ENST00000288447.8:c.1302A>C	ENSP00000288447.4:p.Gln434His
ENST00000357033.8:c.1326A>C	ENSP00000354923.3:p.Gln442His
ENST00000378677.6:c.1314A>C	ENSP00000367948.2:p.Gln438His
ENST00000420596.5:c.94-278938A>C	ENSP00000399897.1:n.94-278938A>C
ENST00000447523.1:c.247-70291A>C	ENSP00000395904.1:n.247-70291A>C
ENST00000448370.5:c.94-279427A>C	ENSP00000388559.1:n.94-279427A>C
ENST00000480751.1:n.87-70291A>C
ENST00000488902.5:n.335+376002A>C
ENST00000619831.4:c.1314A>C	ENSP00000479270.1:p.Gln438His
ENST00000620040.4:c.1326A>C	ENSP00000478150.1:p.Gln442His
NM_000109.3:c.1302A>C	NP_000100.2:p.Gln434His
NM_004006.2:c.1326A>C , LRG_199t1:c.1326A>C	NP_003997.1:p.Gln442His
NM_004009.3:c.1314A>C	NP_004000.1:p.Gln438His
NM_004010.3:c.957A>C	NP_004001.1:p.Gln319His
XM_006724468.2:c.1326A>C	XP_006724531.1:p.Gln442His
XM_006724469.2:c.1302A>C	XP_006724532.1:p.Gln434His
XM_006724470.2:c.1326A>C	XP_006724533.1:p.Gln442His
XM_006724471.2:c.1326A>C	XP_006724534.1:p.Gln442His
XM_006724472.2:c.1197A>C	XP_006724535.1:p.Gln399His
XM_006724473.2:c.1326A>C	XP_006724536.1:p.Gln442His
XM_006724474.2:c.1326A>C	XP_006724537.1:p.Gln442His
XM_006724475.2:c.1326A>C	XP_006724538.1:p.Gln442His
XM_011545467.1:c.1326A>C	XP_011543769.1:p.Gln442His
XM_011545468.1:c.1326A>C	XP_011543770.1:p.Gln442His
XM_011545469.1:c.1326A>C	XP_011543771.1:p.Gln442His
XM_006724469.3:c.1302A>C	XP_006724532.1:p.Gln434His
XM_006724470.3:c.1326A>C	XP_006724533.1:p.Gln442His
XM_006724474.3:c.1326A>C	XP_006724537.1:p.Gln442His
XM_011545468.2:c.1326A>C	XP_011543770.1:p.Gln442His
XM_017029328.1:c.1326A>C	XP_016884817.1:p.Gln442His
XM_017029329.1:c.1326A>C	XP_016884818.1:p.Gln442His
XM_017029330.2:c.1326A>C	XP_016884819.1:p.Gln442His
NM_000109.4:c.1302A>C	NP_000100.3:p.Gln434His
NM_004006.3:c.1326A>C MANE Select	NP_003997.2:p.Gln442His