Canonical Allele Identifier: CA412658802

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.31792128C>A (hg19) ; chrX:g.31774011C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31774011C>A , CM000685.2:g.31774011C>A	GRCh38
NC_000023.10:g.31792128C>A , CM000685.1:g.31792128C>A	GRCh37
NC_000023.9:g.31702049C>A	NCBI36
NG_012232.1:g.1570599G>T , LRG_199:g.1570599G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.2337G>T	ENSP00000350765.3:p.Arg779Ser
ENST00000682238.1:c.111G>T	ENSP00000508124.1:p.Arg37Ser
ENST00000683117.1:n.1152G>T
ENST00000683450.1:n.1074G>T
ENST00000683851.1:n.1152G>T
ENST00000683957.1:n.983G>T
ENST00000684130.1:c.111G>T	ENSP00000508037.1:p.Arg37Ser
ENST00000357033.9:c.7491G>T MANE Select	ENSP00000354923.3:p.Arg2497Ser
ENST00000619831.5:c.3459G>T	ENSP00000479270.2:p.Arg1153Ser
ENST00000620040.5:c.111G>T	ENSP00000478150.2:p.Arg37Ser
ENST00000680961.1:c.111G>T	ENSP00000506386.1:p.Arg37Ser
ENST00000681646.1:n.1152G>T
ENST00000681839.1:c.480G>T	ENSP00000505228.1:p.Arg160Ser
ENST00000357033.8:c.7491G>T	ENSP00000354923.3:p.Arg2497Ser
ENST00000358062.6:c.579G>T	ENSP00000350765.2:p.Arg193Ser
ENST00000359836.5:c.111G>T	ENSP00000352894.1:p.Arg37Ser
ENST00000378677.6:c.7479G>T	ENSP00000367948.2:p.Arg2493Ser
ENST00000378707.7:c.111G>T	ENSP00000367979.3:p.Arg37Ser
ENST00000471779.1:c.248G>T	ENSP00000417075.1:n.248G>T
ENST00000474231.5:c.111G>T	ENSP00000417123.1:p.Arg37Ser
ENST00000541735.5:c.111G>T	ENSP00000444119.1:p.Arg37Ser
ENST00000619831.4:c.7476G>T	ENSP00000479270.1:p.Arg2492Ser
ENST00000620040.4:c.7488G>T	ENSP00000478150.1:p.Arg2496Ser
NM_000109.3:c.7467G>T	NP_000100.2:p.Arg2489Ser
NM_004006.2:c.7491G>T , LRG_199t1:c.7491G>T	NP_003997.1:p.Arg2497Ser
NM_004009.3:c.7479G>T	NP_004000.1:p.Arg2493Ser
NM_004010.3:c.7122G>T	NP_004001.1:p.Arg2374Ser
NM_004011.3:c.3468G>T	NP_004002.2:p.Arg1156Ser
NM_004012.3:c.3459G>T	NP_004003.1:p.Arg1153Ser
NM_004013.2:c.111G>T	NP_004004.1:p.Arg37Ser
NM_004020.3:c.111G>T	NP_004011.2:p.Arg37Ser
NM_004021.2:c.111G>T	NP_004012.1:p.Arg37Ser
NM_004022.2:c.111G>T	NP_004013.1:p.Arg37Ser
NM_004023.2:c.111G>T	NP_004014.1:p.Arg37Ser
XM_006724468.2:c.7491G>T	XP_006724531.1:p.Arg2497Ser
XM_006724469.2:c.7467G>T	XP_006724532.1:p.Arg2489Ser
XM_006724470.2:c.7491G>T	XP_006724533.1:p.Arg2497Ser
XM_006724471.2:c.7491G>T	XP_006724534.1:p.Arg2497Ser
XM_006724472.2:c.7362G>T	XP_006724535.1:p.Arg2454Ser
XM_006724473.2:c.7353G>T	XP_006724536.1:p.Arg2451Ser
XM_006724474.2:c.7491G>T	XP_006724537.1:p.Arg2497Ser
XM_006724475.2:c.7491G>T	XP_006724538.1:p.Arg2497Ser
XM_011545467.1:c.7368G>T	XP_011543769.1:p.Arg2456Ser
XM_011545468.1:c.7491G>T	XP_011543770.1:p.Arg2497Ser
XM_006724469.3:c.7467G>T	XP_006724532.1:p.Arg2489Ser
XM_006724470.3:c.7491G>T	XP_006724533.1:p.Arg2497Ser
XM_006724474.3:c.7491G>T	XP_006724537.1:p.Arg2497Ser
XM_011545468.2:c.7491G>T	XP_011543770.1:p.Arg2497Ser
XM_017029328.1:c.7491G>T	XP_016884817.1:p.Arg2497Ser
XM_017029331.1:c.1665G>T	XP_016884820.1:p.Arg555Ser
NM_000109.4:c.7467G>T	NP_000100.3:p.Arg2489Ser
NM_004006.3:c.7491G>T MANE Select	NP_003997.2:p.Arg2497Ser
NM_004011.4:c.3468G>T	NP_004002.3:p.Arg1156Ser
NM_004012.4:c.3459G>T	NP_004003.2:p.Arg1153Ser
NM_004021.3:c.111G>T	NP_004012.2:p.Arg37Ser
NM_004023.3:c.111G>T	NP_004014.2:p.Arg37Ser
NM_004013.3:c.111G>T	NP_004004.2:p.Arg37Ser
NM_004020.4:c.111G>T	NP_004011.3:p.Arg37Ser
NM_004022.3:c.111G>T	NP_004013.2:p.Arg37Ser