Canonical Allele Identifier: CA412658646

Gene: DMD

Linked Data

• dbSNP Id: rs1207135550
• gnomAD v2: X-31792093-A-G
• MyVariant Identifiers: chrX:g.31792093A>G (hg19) ; chrX:g.31773976A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31773976A>G , CM000685.2:g.31773976A>G	GRCh38
NC_000023.10:g.31792093A>G , CM000685.1:g.31792093A>G	GRCh37
NC_000023.9:g.31702014A>G	NCBI36
NG_012232.1:g.1570634T>C , LRG_199:g.1570634T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.2372T>C	ENSP00000350765.3:p.Met791Thr
ENST00000682238.1:c.146T>C	ENSP00000508124.1:p.Met49Thr
ENST00000683117.1:n.1187T>C
ENST00000683450.1:n.1109T>C
ENST00000683851.1:n.1187T>C
ENST00000683957.1:n.1018T>C
ENST00000684130.1:c.146T>C	ENSP00000508037.1:p.Met49Thr
ENST00000357033.9:c.7526T>C MANE Select	ENSP00000354923.3:p.Met2509Thr
ENST00000619831.5:c.3494T>C	ENSP00000479270.2:p.Met1165Thr
ENST00000620040.5:c.146T>C	ENSP00000478150.2:p.Met49Thr
ENST00000680961.1:c.146T>C	ENSP00000506386.1:p.Met49Thr
ENST00000681646.1:n.1187T>C
ENST00000681839.1:c.515T>C	ENSP00000505228.1:p.Met172Thr
ENST00000357033.8:c.7526T>C	ENSP00000354923.3:p.Met2509Thr
ENST00000358062.6:c.614T>C	ENSP00000350765.2:p.Met205Thr
ENST00000359836.5:c.146T>C	ENSP00000352894.1:p.Met49Thr
ENST00000378677.6:c.7514T>C	ENSP00000367948.2:p.Met2505Thr
ENST00000378707.7:c.146T>C	ENSP00000367979.3:p.Met49Thr
ENST00000471779.1:c.283T>C	ENSP00000417075.1:n.283T>C
ENST00000474231.5:c.146T>C	ENSP00000417123.1:p.Met49Thr
ENST00000541735.5:c.146T>C	ENSP00000444119.1:p.Met49Thr
ENST00000619831.4:c.7511T>C	ENSP00000479270.1:p.Met2504Thr
ENST00000620040.4:c.7523T>C	ENSP00000478150.1:p.Met2508Thr
NM_000109.3:c.7502T>C	NP_000100.2:p.Met2501Thr
NM_004006.2:c.7526T>C , LRG_199t1:c.7526T>C	NP_003997.1:p.Met2509Thr
NM_004009.3:c.7514T>C	NP_004000.1:p.Met2505Thr
NM_004010.3:c.7157T>C	NP_004001.1:p.Met2386Thr
NM_004011.3:c.3503T>C	NP_004002.2:p.Met1168Thr
NM_004012.3:c.3494T>C	NP_004003.1:p.Met1165Thr
NM_004013.2:c.146T>C	NP_004004.1:p.Met49Thr
NM_004020.3:c.146T>C	NP_004011.2:p.Met49Thr
NM_004021.2:c.146T>C	NP_004012.1:p.Met49Thr
NM_004022.2:c.146T>C	NP_004013.1:p.Met49Thr
NM_004023.2:c.146T>C	NP_004014.1:p.Met49Thr
XM_006724468.2:c.7526T>C	XP_006724531.1:p.Met2509Thr
XM_006724469.2:c.7502T>C	XP_006724532.1:p.Met2501Thr
XM_006724470.2:c.7526T>C	XP_006724533.1:p.Met2509Thr
XM_006724471.2:c.7526T>C	XP_006724534.1:p.Met2509Thr
XM_006724472.2:c.7397T>C	XP_006724535.1:p.Met2466Thr
XM_006724473.2:c.7388T>C	XP_006724536.1:p.Met2463Thr
XM_006724474.2:c.7526T>C	XP_006724537.1:p.Met2509Thr
XM_006724475.2:c.7526T>C	XP_006724538.1:p.Met2509Thr
XM_011545467.1:c.7403T>C	XP_011543769.1:p.Met2468Thr
XM_011545468.1:c.7526T>C	XP_011543770.1:p.Met2509Thr
XM_006724469.3:c.7502T>C	XP_006724532.1:p.Met2501Thr
XM_006724470.3:c.7526T>C	XP_006724533.1:p.Met2509Thr
XM_006724474.3:c.7526T>C	XP_006724537.1:p.Met2509Thr
XM_011545468.2:c.7526T>C	XP_011543770.1:p.Met2509Thr
XM_017029328.1:c.7526T>C	XP_016884817.1:p.Met2509Thr
XM_017029331.1:c.1700T>C	XP_016884820.1:p.Met567Thr
NM_000109.4:c.7502T>C	NP_000100.3:p.Met2501Thr
NM_004006.3:c.7526T>C MANE Select	NP_003997.2:p.Met2509Thr
NM_004011.4:c.3503T>C	NP_004002.3:p.Met1168Thr
NM_004012.4:c.3494T>C	NP_004003.2:p.Met1165Thr
NM_004021.3:c.146T>C	NP_004012.2:p.Met49Thr
NM_004023.3:c.146T>C	NP_004014.2:p.Met49Thr
NM_004013.3:c.146T>C	NP_004004.2:p.Met49Thr
NM_004020.4:c.146T>C	NP_004011.3:p.Met49Thr
NM_004022.3:c.146T>C	NP_004013.2:p.Met49Thr