Canonical Allele Identifier: CA412660177

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31875329T>G , CM000685.2:g.31875329T>G	GRCh38
NC_000023.10:g.31893446T>G , CM000685.1:g.31893446T>G	GRCh37
NC_000023.9:g.31803367T>G	NCBI36
NG_012232.1:g.1469281A>C , LRG_199:g.1469281A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004006.3:c.6957A>C MANE Select	NP_003997.2:p.Gln2319His
ENST00000357033.9:c.6957A>C MANE Select	ENSP00000354923.3:p.Gln2319His
NM_000109.3:c.6933A>C	NP_000100.2:p.Gln2311His
NM_000109.4:c.6933A>C	NP_000100.3:p.Gln2311His
NM_004006.2:c.6957A>C , LRG_199t1:c.6957A>C	NP_003997.1:p.Gln2319His
NM_004009.3:c.6945A>C	NP_004000.1:p.Gln2315His
NM_004010.3:c.6588A>C	NP_004001.1:p.Gln2196His
NM_004011.3:c.2934A>C	NP_004002.2:p.Gln978His
NM_004011.4:c.2934A>C	NP_004002.3:p.Gln978His
NM_004012.3:c.2925A>C	NP_004003.1:p.Gln975His
NM_004012.4:c.2925A>C	NP_004003.2:p.Gln975His
NM_004013.2:c.-424A>C	NP_004004.1:n.-424A>C
NM_004013.3:c.-424A>C	NP_004004.2:n.-424A>C
NM_004020.3:c.-424A>C	NP_004011.2:n.-424A>C
NM_004020.4:c.-424A>C	NP_004011.3:n.-424A>C
NM_004021.2:c.-424A>C	NP_004012.1:n.-424A>C
NM_004021.3:c.-424A>C	NP_004012.2:n.-424A>C
NM_004022.2:c.-424A>C	NP_004013.1:n.-424A>C
NM_004022.3:c.-424A>C	NP_004013.2:n.-424A>C
NM_004023.2:c.-424A>C	NP_004014.1:n.-424A>C
NM_004023.3:c.-424A>C	NP_004014.2:n.-424A>C
ENST00000357033.8:c.6957A>C	ENSP00000354923.3:p.Gln2319His
ENST00000358062.6:c.45A>C	ENSP00000350765.2:p.Gln15His
ENST00000358062.7:c.1803A>C	ENSP00000350765.3:p.Gln601His
ENST00000359836.5:c.-424A>C	ENSP00000352894.1:n.-424A>C
ENST00000378677.6:c.6945A>C	ENSP00000367948.2:p.Gln2315His
ENST00000378707.7:c.-424A>C	ENSP00000367979.3:n.-424A>C
ENST00000474231.5:c.-424A>C	ENSP00000417123.1:n.-424A>C
ENST00000541735.5:c.-424A>C	ENSP00000444119.1:n.-424A>C
ENST00000619831.4:c.6942A>C	ENSP00000479270.1:p.Gln2314His
ENST00000619831.5:c.2925A>C	ENSP00000479270.2:p.Gln975His
ENST00000620040.4:c.6954A>C	ENSP00000478150.1:p.Gln2318His
ENST00000620040.5:c.-424A>C	ENSP00000478150.2:n.-424A>C
ENST00000680961.1:c.-424A>C	ENSP00000506386.1:n.-424A>C
ENST00000681646.1:n.618A>C
ENST00000682238.1:c.-424A>C	ENSP00000508124.1:n.-424A>C
ENST00000683117.1:n.618A>C
ENST00000683450.1:n.540A>C
ENST00000683851.1:n.618A>C
ENST00000683957.1:n.449A>C
ENST00000684130.1:c.-424A>C	ENSP00000508037.1:n.-424A>C
XM_006724468.2:c.6957A>C	XP_006724531.1:p.Gln2319His
XM_006724469.2:c.6933A>C	XP_006724532.1:p.Gln2311His
XM_006724469.3:c.6933A>C	XP_006724532.1:p.Gln2311His
XM_006724470.2:c.6957A>C	XP_006724533.1:p.Gln2319His
XM_006724470.3:c.6957A>C	XP_006724533.1:p.Gln2319His
XM_006724471.2:c.6957A>C	XP_006724534.1:p.Gln2319His
XM_006724472.2:c.6828A>C	XP_006724535.1:p.Gln2276His
XM_006724473.2:c.6819A>C	XP_006724536.1:p.Gln2273His
XM_006724474.2:c.6957A>C	XP_006724537.1:p.Gln2319His
XM_006724474.3:c.6957A>C	XP_006724537.1:p.Gln2319His
XM_006724475.2:c.6957A>C	XP_006724538.1:p.Gln2319His
XM_011545467.1:c.6834A>C	XP_011543769.1:p.Gln2278His
XM_011545468.1:c.6957A>C	XP_011543770.1:p.Gln2319His
XM_011545468.2:c.6957A>C	XP_011543770.1:p.Gln2319His
XM_017029328.1:c.6957A>C	XP_016884817.1:p.Gln2319His
XM_017029331.1:c.1131A>C	XP_016884820.1:p.Gln377His