Canonical Allele Identifier: CA412659122

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.31792270A>T (hg19) ; chrX:g.31774153A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31774153A>T , CM000685.2:g.31774153A>T	GRCh38
NC_000023.10:g.31792270A>T , CM000685.1:g.31792270A>T	GRCh37
NC_000023.9:g.31702191A>T	NCBI36
NG_012232.1:g.1570457T>A , LRG_199:g.1570457T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.2195T>A	ENSP00000350765.3:p.Val732Asp
ENST00000682238.1:c.-32T>A	ENSP00000508124.1:n.-32T>A
ENST00000683117.1:n.1010T>A
ENST00000683450.1:n.932T>A
ENST00000683851.1:n.1010T>A
ENST00000683957.1:n.841T>A
ENST00000684130.1:c.-32T>A	ENSP00000508037.1:n.-32T>A
ENST00000357033.9:c.7349T>A MANE Select	ENSP00000354923.3:p.Val2450Asp
ENST00000619831.5:c.3317T>A	ENSP00000479270.2:p.Val1106Asp
ENST00000620040.5:c.-32T>A	ENSP00000478150.2:n.-32T>A
ENST00000680961.1:c.-32T>A	ENSP00000506386.1:n.-32T>A
ENST00000681646.1:n.1010T>A
ENST00000681839.1:c.338T>A	ENSP00000505228.1:p.Val113Asp
ENST00000357033.8:c.7349T>A	ENSP00000354923.3:p.Val2450Asp
ENST00000358062.6:c.437T>A	ENSP00000350765.2:p.Val146Asp
ENST00000359836.5:c.-32T>A	ENSP00000352894.1:n.-32T>A
ENST00000378677.6:c.7337T>A	ENSP00000367948.2:p.Val2446Asp
ENST00000378707.7:c.-32T>A	ENSP00000367979.3:n.-32T>A
ENST00000471779.1:c.106T>A	ENSP00000417075.1:n.106T>A
ENST00000474231.5:c.-32T>A	ENSP00000417123.1:n.-32T>A
ENST00000541735.5:c.-32T>A	ENSP00000444119.1:n.-32T>A
ENST00000619831.4:c.7334T>A	ENSP00000479270.1:p.Val2445Asp
ENST00000620040.4:c.7346T>A	ENSP00000478150.1:p.Val2449Asp
NM_000109.3:c.7325T>A	NP_000100.2:p.Val2442Asp
NM_004006.2:c.7349T>A , LRG_199t1:c.7349T>A	NP_003997.1:p.Val2450Asp
NM_004009.3:c.7337T>A	NP_004000.1:p.Val2446Asp
NM_004010.3:c.6980T>A	NP_004001.1:p.Val2327Asp
NM_004011.3:c.3326T>A	NP_004002.2:p.Val1109Asp
NM_004012.3:c.3317T>A	NP_004003.1:p.Val1106Asp
NM_004013.2:c.-32T>A	NP_004004.1:n.-32T>A
NM_004020.3:c.-32T>A	NP_004011.2:n.-32T>A
NM_004021.2:c.-32T>A	NP_004012.1:n.-32T>A
NM_004022.2:c.-32T>A	NP_004013.1:n.-32T>A
NM_004023.2:c.-32T>A	NP_004014.1:n.-32T>A
XM_006724468.2:c.7349T>A	XP_006724531.1:p.Val2450Asp
XM_006724469.2:c.7325T>A	XP_006724532.1:p.Val2442Asp
XM_006724470.2:c.7349T>A	XP_006724533.1:p.Val2450Asp
XM_006724471.2:c.7349T>A	XP_006724534.1:p.Val2450Asp
XM_006724472.2:c.7220T>A	XP_006724535.1:p.Val2407Asp
XM_006724473.2:c.7211T>A	XP_006724536.1:p.Val2404Asp
XM_006724474.2:c.7349T>A	XP_006724537.1:p.Val2450Asp
XM_006724475.2:c.7349T>A	XP_006724538.1:p.Val2450Asp
XM_011545467.1:c.7226T>A	XP_011543769.1:p.Val2409Asp
XM_011545468.1:c.7349T>A	XP_011543770.1:p.Val2450Asp
XM_006724469.3:c.7325T>A	XP_006724532.1:p.Val2442Asp
XM_006724470.3:c.7349T>A	XP_006724533.1:p.Val2450Asp
XM_006724474.3:c.7349T>A	XP_006724537.1:p.Val2450Asp
XM_011545468.2:c.7349T>A	XP_011543770.1:p.Val2450Asp
XM_017029328.1:c.7349T>A	XP_016884817.1:p.Val2450Asp
XM_017029331.1:c.1523T>A	XP_016884820.1:p.Val508Asp
NM_000109.4:c.7325T>A	NP_000100.3:p.Val2442Asp
NM_004006.3:c.7349T>A MANE Select	NP_003997.2:p.Val2450Asp
NM_004011.4:c.3326T>A	NP_004002.3:p.Val1109Asp
NM_004012.4:c.3317T>A	NP_004003.2:p.Val1106Asp
NM_004021.3:c.-32T>A	NP_004012.2:n.-32T>A
NM_004023.3:c.-32T>A	NP_004014.2:n.-32T>A
NM_004013.3:c.-32T>A	NP_004004.2:n.-32T>A
NM_004020.4:c.-32T>A	NP_004011.3:n.-32T>A
NM_004022.3:c.-32T>A	NP_004013.2:n.-32T>A