Canonical Allele Identifier: CA412655076

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.31462620T>G (hg19) ; chrX:g.31444503T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31444503T>G , CM000685.2:g.31444503T>G	GRCh38
NC_000023.10:g.31462620T>G , CM000685.1:g.31462620T>G	GRCh37
NC_000023.9:g.31372541T>G	NCBI36
NG_012232.1:g.1900107A>C , LRG_199:g.1900107A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.3908A>C	ENSP00000350765.3:p.Asn1303Thr
ENST00000682238.1:c.1682A>C	ENSP00000508124.1:p.Asn561Thr
ENST00000683450.1:n.2527A>C
ENST00000683957.1:n.2554A>C
ENST00000684130.1:c.1682A>C	ENSP00000508037.1:p.Asn561Thr
ENST00000343523.7:c.917A>C	ENSP00000340057.4:p.Asn306Thr
ENST00000357033.9:c.9062A>C MANE Select	ENSP00000354923.3:p.Asn3021Thr
ENST00000619831.5:c.5030A>C	ENSP00000479270.2:p.Asn1677Thr
ENST00000620040.5:c.1682A>C	ENSP00000478150.2:p.Asn561Thr
ENST00000680961.1:c.1682A>C	ENSP00000506386.1:p.Asn561Thr
ENST00000681646.1:n.2723A>C
ENST00000343523.6:c.875A>C	ENSP00000340057.3:p.Asn292Thr
ENST00000357033.8:c.9062A>C	ENSP00000354923.3:p.Asn3021Thr
ENST00000358062.6:c.2150A>C	ENSP00000350765.2:p.Asn717Thr
ENST00000359836.5:c.1682A>C	ENSP00000352894.1:p.Asn561Thr
ENST00000378677.6:c.9050A>C	ENSP00000367948.2:p.Asn3017Thr
ENST00000378707.7:c.1682A>C	ENSP00000367979.3:p.Asn561Thr
ENST00000474231.5:c.1682A>C	ENSP00000417123.1:p.Asn561Thr
ENST00000541735.5:c.1682A>C	ENSP00000444119.1:p.Asn561Thr
ENST00000619831.4:c.9047A>C	ENSP00000479270.1:p.Asn3016Thr
ENST00000620040.4:c.9059A>C	ENSP00000478150.1:p.Asn3020Thr
NM_000109.3:c.9038A>C	NP_000100.2:p.Asn3013Thr
NM_004006.2:c.9062A>C , LRG_199t1:c.9062A>C	NP_003997.1:p.Asn3021Thr
NM_004009.3:c.9050A>C	NP_004000.1:p.Asn3017Thr
NM_004010.3:c.8693A>C	NP_004001.1:p.Asn2898Thr
NM_004011.3:c.5039A>C	NP_004002.2:p.Asn1680Thr
NM_004012.3:c.5030A>C	NP_004003.1:p.Asn1677Thr
NM_004013.2:c.1682A>C	NP_004004.1:p.Asn561Thr
NM_004014.2:c.875A>C	NP_004005.1:p.Asn292Thr
NM_004020.3:c.1682A>C	NP_004011.2:p.Asn561Thr
NM_004021.2:c.1682A>C	NP_004012.1:p.Asn561Thr
NM_004022.2:c.1682A>C	NP_004013.1:p.Asn561Thr
NM_004023.2:c.1682A>C	NP_004014.1:p.Asn561Thr
XM_006724468.2:c.9062A>C	XP_006724531.1:p.Asn3021Thr
XM_006724469.2:c.9038A>C	XP_006724532.1:p.Asn3013Thr
XM_006724470.2:c.9062A>C	XP_006724533.1:p.Asn3021Thr
XM_006724471.2:c.9062A>C	XP_006724534.1:p.Asn3021Thr
XM_006724472.2:c.8933A>C	XP_006724535.1:p.Asn2978Thr
XM_006724473.2:c.8924A>C	XP_006724536.1:p.Asn2975Thr
XM_006724474.2:c.9062A>C	XP_006724537.1:p.Asn3021Thr
XM_006724475.2:c.9062A>C	XP_006724538.1:p.Asn3021Thr
XM_011545467.1:c.8939A>C	XP_011543769.1:p.Asn2980Thr
XM_011545468.1:c.9062A>C	XP_011543770.1:p.Asn3021Thr
XM_006724469.3:c.9038A>C	XP_006724532.1:p.Asn3013Thr
XM_006724470.3:c.9062A>C	XP_006724533.1:p.Asn3021Thr
XM_006724474.3:c.9062A>C	XP_006724537.1:p.Asn3021Thr
XM_011545468.2:c.9062A>C	XP_011543770.1:p.Asn3021Thr
XM_017029328.1:c.9062A>C	XP_016884817.1:p.Asn3021Thr
XM_017029331.1:c.3236A>C	XP_016884820.1:p.Asn1079Thr
NM_000109.4:c.9038A>C	NP_000100.3:p.Asn3013Thr
NM_004006.3:c.9062A>C MANE Select	NP_003997.2:p.Asn3021Thr
NM_004011.4:c.5039A>C	NP_004002.3:p.Asn1680Thr
NM_004012.4:c.5030A>C	NP_004003.2:p.Asn1677Thr
NM_004021.3:c.1682A>C	NP_004012.2:p.Asn561Thr
NM_004023.3:c.1682A>C	NP_004014.2:p.Asn561Thr
NM_004013.3:c.1682A>C	NP_004004.2:p.Asn561Thr
NM_004014.3:c.875A>C	NP_004005.2:p.Asn292Thr
NM_004020.4:c.1682A>C	NP_004011.3:p.Asn561Thr
NM_004022.3:c.1682A>C	NP_004013.2:p.Asn561Thr