Canonical Allele Identifier: CA515863251

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.32328310A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32310193A>G , CM000685.2:g.32310193A>G	GRCh38
NC_000023.10:g.32328310A>G , CM000685.1:g.32328310A>G	GRCh37
NC_000023.9:g.32238231A>G	NCBI36
NG_012232.1:g.1034417T>C , LRG_199:g.1034417T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.852T>C	ENSP00000350765.3:p.Thr284=
ENST00000357033.9:c.6006T>C MANE Select	ENSP00000354923.3:p.Thr2002=
ENST00000619831.5:c.1974T>C	ENSP00000479270.2:p.Thr658=
ENST00000357033.8:c.6006T>C	ENSP00000354923.3:p.Thr2002=
ENST00000378677.6:c.5994T>C	ENSP00000367948.2:p.Thr1998=
ENST00000488902.5:n.336-93130T>C
ENST00000619831.4:c.5994T>C	ENSP00000479270.1:p.Thr1998=
ENST00000620040.4:c.6006T>C	ENSP00000478150.1:p.Thr2002=
NM_000109.3:c.5982T>C	NP_000100.2:p.Thr1994=
NM_004006.2:c.6006T>C , LRG_199t1:c.6006T>C	NP_003997.1:p.Thr2002=
NM_004009.3:c.5994T>C	NP_004000.1:p.Thr1998=
NM_004010.3:c.5637T>C	NP_004001.1:p.Thr1879=
NM_004011.3:c.1983T>C	NP_004002.2:p.Thr661=
NM_004012.3:c.1974T>C	NP_004003.1:p.Thr658=
XM_006724468.2:c.6006T>C	XP_006724531.1:p.Thr2002=
XM_006724469.2:c.5982T>C	XP_006724532.1:p.Thr1994=
XM_006724470.2:c.6006T>C	XP_006724533.1:p.Thr2002=
XM_006724471.2:c.6006T>C	XP_006724534.1:p.Thr2002=
XM_006724472.2:c.5877T>C	XP_006724535.1:p.Thr1959=
XM_006724473.2:c.5868T>C	XP_006724536.1:p.Thr1956=
XM_006724474.2:c.6006T>C	XP_006724537.1:p.Thr2002=
XM_006724475.2:c.6006T>C	XP_006724538.1:p.Thr2002=
XM_011545467.1:c.5883T>C	XP_011543769.1:p.Thr1961=
XM_011545468.1:c.6006T>C	XP_011543770.1:p.Thr2002=
XM_006724469.3:c.5982T>C	XP_006724532.1:p.Thr1994=
XM_006724470.3:c.6006T>C	XP_006724533.1:p.Thr2002=
XM_006724474.3:c.6006T>C	XP_006724537.1:p.Thr2002=
XM_011545468.2:c.6006T>C	XP_011543770.1:p.Thr2002=
XM_017029328.1:c.6006T>C	XP_016884817.1:p.Thr2002=
XM_017029329.1:c.6006T>C	XP_016884818.1:p.Thr2002=
XM_017029330.2:c.6006T>C	XP_016884819.1:p.Thr2002=
XM_017029331.1:c.180T>C	XP_016884820.1:p.Thr60=
NM_000109.4:c.5982T>C	NP_000100.3:p.Thr1994=
NM_004006.3:c.6006T>C MANE Select	NP_003997.2:p.Thr2002=
NM_004011.4:c.1983T>C	NP_004002.3:p.Thr661=
NM_004012.4:c.1974T>C	NP_004003.2:p.Thr658=