Canonical Allele Identifier: CA328429792

Gene: DMD

Linked Data

• dbSNP Id: rs1036865168
• gnomAD v4: X-31444611-A-G
• MyVariant Identifiers: chrX:g.31462728A>G (hg19) ; chrX:g.31444611A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31444611A>G , CM000685.2:g.31444611A>G	GRCh38
NC_000023.10:g.31462728A>G , CM000685.1:g.31462728A>G	GRCh37
NC_000023.9:g.31372649A>G	NCBI36
NG_012232.1:g.1899999T>C , LRG_199:g.1899999T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.3800T>C	ENSP00000350765.3:p.Ile1267Thr
ENST00000682238.1:c.1574T>C	ENSP00000508124.1:p.Ile525Thr
ENST00000683450.1:n.2419T>C
ENST00000683957.1:n.2446T>C
ENST00000684130.1:c.1574T>C	ENSP00000508037.1:p.Ile525Thr
ENST00000343523.7:c.809T>C	ENSP00000340057.4:p.Ile270Thr
ENST00000357033.9:c.8954T>C MANE Select	ENSP00000354923.3:p.Ile2985Thr
ENST00000619831.5:c.4922T>C	ENSP00000479270.2:p.Ile1641Thr
ENST00000620040.5:c.1574T>C	ENSP00000478150.2:p.Ile525Thr
ENST00000680961.1:c.1574T>C	ENSP00000506386.1:p.Ile525Thr
ENST00000681646.1:n.2615T>C
ENST00000343523.6:c.767T>C	ENSP00000340057.3:p.Ile256Thr
ENST00000357033.8:c.8954T>C	ENSP00000354923.3:p.Ile2985Thr
ENST00000358062.6:c.2042T>C	ENSP00000350765.2:p.Ile681Thr
ENST00000359836.5:c.1574T>C	ENSP00000352894.1:p.Ile525Thr
ENST00000378677.6:c.8942T>C	ENSP00000367948.2:p.Ile2981Thr
ENST00000378707.7:c.1574T>C	ENSP00000367979.3:p.Ile525Thr
ENST00000474231.5:c.1574T>C	ENSP00000417123.1:p.Ile525Thr
ENST00000541735.5:c.1574T>C	ENSP00000444119.1:p.Ile525Thr
ENST00000619831.4:c.8939T>C	ENSP00000479270.1:p.Ile2980Thr
ENST00000620040.4:c.8951T>C	ENSP00000478150.1:p.Ile2984Thr
NM_000109.3:c.8930T>C	NP_000100.2:p.Ile2977Thr
NM_004006.2:c.8954T>C , LRG_199t1:c.8954T>C	NP_003997.1:p.Ile2985Thr
NM_004009.3:c.8942T>C	NP_004000.1:p.Ile2981Thr
NM_004010.3:c.8585T>C	NP_004001.1:p.Ile2862Thr
NM_004011.3:c.4931T>C	NP_004002.2:p.Ile1644Thr
NM_004012.3:c.4922T>C	NP_004003.1:p.Ile1641Thr
NM_004013.2:c.1574T>C	NP_004004.1:p.Ile525Thr
NM_004014.2:c.767T>C	NP_004005.1:p.Ile256Thr
NM_004020.3:c.1574T>C	NP_004011.2:p.Ile525Thr
NM_004021.2:c.1574T>C	NP_004012.1:p.Ile525Thr
NM_004022.2:c.1574T>C	NP_004013.1:p.Ile525Thr
NM_004023.2:c.1574T>C	NP_004014.1:p.Ile525Thr
XM_006724468.2:c.8954T>C	XP_006724531.1:p.Ile2985Thr
XM_006724469.2:c.8930T>C	XP_006724532.1:p.Ile2977Thr
XM_006724470.2:c.8954T>C	XP_006724533.1:p.Ile2985Thr
XM_006724471.2:c.8954T>C	XP_006724534.1:p.Ile2985Thr
XM_006724472.2:c.8825T>C	XP_006724535.1:p.Ile2942Thr
XM_006724473.2:c.8816T>C	XP_006724536.1:p.Ile2939Thr
XM_006724474.2:c.8954T>C	XP_006724537.1:p.Ile2985Thr
XM_006724475.2:c.8954T>C	XP_006724538.1:p.Ile2985Thr
XM_011545467.1:c.8831T>C	XP_011543769.1:p.Ile2944Thr
XM_011545468.1:c.8954T>C	XP_011543770.1:p.Ile2985Thr
XM_006724469.3:c.8930T>C	XP_006724532.1:p.Ile2977Thr
XM_006724470.3:c.8954T>C	XP_006724533.1:p.Ile2985Thr
XM_006724474.3:c.8954T>C	XP_006724537.1:p.Ile2985Thr
XM_011545468.2:c.8954T>C	XP_011543770.1:p.Ile2985Thr
XM_017029328.1:c.8954T>C	XP_016884817.1:p.Ile2985Thr
XM_017029331.1:c.3128T>C	XP_016884820.1:p.Ile1043Thr
NM_000109.4:c.8930T>C	NP_000100.3:p.Ile2977Thr
NM_004006.3:c.8954T>C MANE Select	NP_003997.2:p.Ile2985Thr
NM_004011.4:c.4931T>C	NP_004002.3:p.Ile1644Thr
NM_004012.4:c.4922T>C	NP_004003.2:p.Ile1641Thr
NM_004021.3:c.1574T>C	NP_004012.2:p.Ile525Thr
NM_004023.3:c.1574T>C	NP_004014.2:p.Ile525Thr
NM_004013.3:c.1574T>C	NP_004004.2:p.Ile525Thr
NM_004014.3:c.767T>C	NP_004005.2:p.Ile256Thr
NM_004020.4:c.1574T>C	NP_004011.3:p.Ile525Thr
NM_004022.3:c.1574T>C	NP_004013.2:p.Ile525Thr