Canonical Allele Identifier: CA412658975

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.31792202C>T (hg19) ; chrX:g.31774085C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31774085C>T , CM000685.2:g.31774085C>T	GRCh38
NC_000023.10:g.31792202C>T , CM000685.1:g.31792202C>T	GRCh37
NC_000023.9:g.31702123C>T	NCBI36
NG_012232.1:g.1570525G>A , LRG_199:g.1570525G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000358062.7:c.2263G>A	ENSP00000350765.3:p.Ala755Thr
ENST00000682238.1:c.37G>A	ENSP00000508124.1:p.Ala13Thr
ENST00000683117.1:n.1078G>A
ENST00000683450.1:n.1000G>A
ENST00000683851.1:n.1078G>A
ENST00000683957.1:n.909G>A
ENST00000684130.1:c.37G>A	ENSP00000508037.1:p.Ala13Thr
ENST00000357033.9:c.7417G>A MANE Select	ENSP00000354923.3:p.Ala2473Thr
ENST00000619831.5:c.3385G>A	ENSP00000479270.2:p.Ala1129Thr
ENST00000620040.5:c.37G>A	ENSP00000478150.2:p.Ala13Thr
ENST00000680961.1:c.37G>A	ENSP00000506386.1:p.Ala13Thr
ENST00000681646.1:n.1078G>A
ENST00000681839.1:c.406G>A	ENSP00000505228.1:p.Ala136Thr
ENST00000357033.8:c.7417G>A	ENSP00000354923.3:p.Ala2473Thr
ENST00000358062.6:c.505G>A	ENSP00000350765.2:p.Ala169Thr
ENST00000359836.5:c.37G>A	ENSP00000352894.1:p.Ala13Thr
ENST00000378677.6:c.7405G>A	ENSP00000367948.2:p.Ala2469Thr
ENST00000378707.7:c.37G>A	ENSP00000367979.3:p.Ala13Thr
ENST00000471779.1:c.174G>A	ENSP00000417075.1:n.174G>A
ENST00000474231.5:c.37G>A	ENSP00000417123.1:p.Ala13Thr
ENST00000541735.5:c.37G>A	ENSP00000444119.1:p.Ala13Thr
ENST00000619831.4:c.7402G>A	ENSP00000479270.1:p.Ala2468Thr
ENST00000620040.4:c.7414G>A	ENSP00000478150.1:p.Ala2472Thr
NM_000109.3:c.7393G>A	NP_000100.2:p.Ala2465Thr
NM_004006.2:c.7417G>A , LRG_199t1:c.7417G>A	NP_003997.1:p.Ala2473Thr
NM_004009.3:c.7405G>A	NP_004000.1:p.Ala2469Thr
NM_004010.3:c.7048G>A	NP_004001.1:p.Ala2350Thr
NM_004011.3:c.3394G>A	NP_004002.2:p.Ala1132Thr
NM_004012.3:c.3385G>A	NP_004003.1:p.Ala1129Thr
NM_004013.2:c.37G>A	NP_004004.1:p.Ala13Thr
NM_004020.3:c.37G>A	NP_004011.2:p.Ala13Thr
NM_004021.2:c.37G>A	NP_004012.1:p.Ala13Thr
NM_004022.2:c.37G>A	NP_004013.1:p.Ala13Thr
NM_004023.2:c.37G>A	NP_004014.1:p.Ala13Thr
XM_006724468.2:c.7417G>A	XP_006724531.1:p.Ala2473Thr
XM_006724469.2:c.7393G>A	XP_006724532.1:p.Ala2465Thr
XM_006724470.2:c.7417G>A	XP_006724533.1:p.Ala2473Thr
XM_006724471.2:c.7417G>A	XP_006724534.1:p.Ala2473Thr
XM_006724472.2:c.7288G>A	XP_006724535.1:p.Ala2430Thr
XM_006724473.2:c.7279G>A	XP_006724536.1:p.Ala2427Thr
XM_006724474.2:c.7417G>A	XP_006724537.1:p.Ala2473Thr
XM_006724475.2:c.7417G>A	XP_006724538.1:p.Ala2473Thr
XM_011545467.1:c.7294G>A	XP_011543769.1:p.Ala2432Thr
XM_011545468.1:c.7417G>A	XP_011543770.1:p.Ala2473Thr
XM_006724469.3:c.7393G>A	XP_006724532.1:p.Ala2465Thr
XM_006724470.3:c.7417G>A	XP_006724533.1:p.Ala2473Thr
XM_006724474.3:c.7417G>A	XP_006724537.1:p.Ala2473Thr
XM_011545468.2:c.7417G>A	XP_011543770.1:p.Ala2473Thr
XM_017029328.1:c.7417G>A	XP_016884817.1:p.Ala2473Thr
XM_017029331.1:c.1591G>A	XP_016884820.1:p.Ala531Thr
NM_000109.4:c.7393G>A	NP_000100.3:p.Ala2465Thr
NM_004006.3:c.7417G>A MANE Select	NP_003997.2:p.Ala2473Thr
NM_004011.4:c.3394G>A	NP_004002.3:p.Ala1132Thr
NM_004012.4:c.3385G>A	NP_004003.2:p.Ala1129Thr
NM_004021.3:c.37G>A	NP_004012.2:p.Ala13Thr
NM_004023.3:c.37G>A	NP_004014.2:p.Ala13Thr
NM_004013.3:c.37G>A	NP_004004.2:p.Ala13Thr
NM_004020.4:c.37G>A	NP_004011.3:p.Ala13Thr
NM_004022.3:c.37G>A	NP_004013.2:p.Ala13Thr