Canonical Allele Identifier: CA412657112

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.31645819C>G (hg19) ; chrX:g.31627702C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31627702C>G , CM000685.2:g.31627702C>G	GRCh38
NC_000023.10:g.31645819C>G , CM000685.1:g.31645819C>G	GRCh37
NC_000023.9:g.31555740C>G	NCBI36
NG_012232.1:g.1716908G>C , LRG_199:g.1716908G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.3034G>C	ENSP00000350765.3:p.Gly1012Arg
ENST00000682238.1:c.808G>C	ENSP00000508124.1:p.Gly270Arg
ENST00000683450.1:n.1653G>C
ENST00000683851.1:n.1849G>C
ENST00000683957.1:n.1680G>C
ENST00000684130.1:c.808G>C	ENSP00000508037.1:p.Gly270Arg
ENST00000357033.9:c.8188G>C MANE Select	ENSP00000354923.3:p.Gly2730Arg
ENST00000619831.5:c.4156G>C	ENSP00000479270.2:p.Gly1386Arg
ENST00000620040.5:c.808G>C	ENSP00000478150.2:p.Gly270Arg
ENST00000680961.1:c.808G>C	ENSP00000506386.1:p.Gly270Arg
ENST00000681646.1:n.1849G>C
ENST00000357033.8:c.8188G>C	ENSP00000354923.3:p.Gly2730Arg
ENST00000358062.6:c.1276G>C	ENSP00000350765.2:p.Gly426Arg
ENST00000359836.5:c.808G>C	ENSP00000352894.1:p.Gly270Arg
ENST00000378677.6:c.8176G>C	ENSP00000367948.2:p.Gly2726Arg
ENST00000378707.7:c.808G>C	ENSP00000367979.3:p.Gly270Arg
ENST00000474231.5:c.808G>C	ENSP00000417123.1:p.Gly270Arg
ENST00000541735.5:c.808G>C	ENSP00000444119.1:p.Gly270Arg
ENST00000619831.4:c.8173G>C	ENSP00000479270.1:p.Gly2725Arg
ENST00000620040.4:c.8185G>C	ENSP00000478150.1:p.Gly2729Arg
NM_000109.3:c.8164G>C	NP_000100.2:p.Gly2722Arg
NM_004006.2:c.8188G>C , LRG_199t1:c.8188G>C	NP_003997.1:p.Gly2730Arg
NM_004009.3:c.8176G>C	NP_004000.1:p.Gly2726Arg
NM_004010.3:c.7819G>C	NP_004001.1:p.Gly2607Arg
NM_004011.3:c.4165G>C	NP_004002.2:p.Gly1389Arg
NM_004012.3:c.4156G>C	NP_004003.1:p.Gly1386Arg
NM_004013.2:c.808G>C	NP_004004.1:p.Gly270Arg
NM_004020.3:c.808G>C	NP_004011.2:p.Gly270Arg
NM_004021.2:c.808G>C	NP_004012.1:p.Gly270Arg
NM_004022.2:c.808G>C	NP_004013.1:p.Gly270Arg
NM_004023.2:c.808G>C	NP_004014.1:p.Gly270Arg
XM_006724468.2:c.8188G>C	XP_006724531.1:p.Gly2730Arg
XM_006724469.2:c.8164G>C	XP_006724532.1:p.Gly2722Arg
XM_006724470.2:c.8188G>C	XP_006724533.1:p.Gly2730Arg
XM_006724471.2:c.8188G>C	XP_006724534.1:p.Gly2730Arg
XM_006724472.2:c.8059G>C	XP_006724535.1:p.Gly2687Arg
XM_006724473.2:c.8050G>C	XP_006724536.1:p.Gly2684Arg
XM_006724474.2:c.8188G>C	XP_006724537.1:p.Gly2730Arg
XM_006724475.2:c.8188G>C	XP_006724538.1:p.Gly2730Arg
XM_011545467.1:c.8065G>C	XP_011543769.1:p.Gly2689Arg
XM_011545468.1:c.8188G>C	XP_011543770.1:p.Gly2730Arg
XM_006724469.3:c.8164G>C	XP_006724532.1:p.Gly2722Arg
XM_006724470.3:c.8188G>C	XP_006724533.1:p.Gly2730Arg
XM_006724474.3:c.8188G>C	XP_006724537.1:p.Gly2730Arg
XM_011545468.2:c.8188G>C	XP_011543770.1:p.Gly2730Arg
XM_017029328.1:c.8188G>C	XP_016884817.1:p.Gly2730Arg
XM_017029331.1:c.2362G>C	XP_016884820.1:p.Gly788Arg
NM_000109.4:c.8164G>C	NP_000100.3:p.Gly2722Arg
NM_004006.3:c.8188G>C MANE Select	NP_003997.2:p.Gly2730Arg
NM_004011.4:c.4165G>C	NP_004002.3:p.Gly1389Arg
NM_004012.4:c.4156G>C	NP_004003.2:p.Gly1386Arg
NM_004021.3:c.808G>C	NP_004012.2:p.Gly270Arg
NM_004023.3:c.808G>C	NP_004014.2:p.Gly270Arg
NM_004013.3:c.808G>C	NP_004004.2:p.Gly270Arg
NM_004020.4:c.808G>C	NP_004011.3:p.Gly270Arg
NM_004022.3:c.808G>C	NP_004013.2:p.Gly270Arg