Canonical Allele Identifier: CA412660277

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31875374C>G , CM000685.2:g.31875374C>G	GRCh38
NC_000023.10:g.31893491C>G , CM000685.1:g.31893491C>G	GRCh37
NC_000023.9:g.31803412C>G	NCBI36
NG_012232.1:g.1469236G>C , LRG_199:g.1469236G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004006.3:c.6913-1G>C MANE Select	NP_003997.2:n.6913-1G>C
ENST00000357033.9:c.6913-1G>C MANE Select	ENSP00000354923.3:n.6913-1G>C
NM_000109.3:c.6889-1G>C	NP_000100.2:n.6889-1G>C
NM_000109.4:c.6889-1G>C	NP_000100.3:n.6889-1G>C
NM_004006.2:c.6913-1G>C , LRG_199t1:c.6913-1G>C	NP_003997.1:n.6913-1G>C
NM_004009.3:c.6901-1G>C	NP_004000.1:n.6901-1G>C
NM_004010.3:c.6544-1G>C	NP_004001.1:n.6544-1G>C
NM_004011.3:c.2890-1G>C	NP_004002.2:n.2890-1G>C
NM_004011.4:c.2890-1G>C	NP_004002.3:n.2890-1G>C
NM_004012.3:c.2881-1G>C	NP_004003.1:n.2881-1G>C
NM_004012.4:c.2881-1G>C	NP_004003.2:n.2881-1G>C
NM_004013.2:c.-468-1G>C	NP_004004.1:n.-468-1G>C
NM_004013.3:c.-468-1G>C	NP_004004.2:n.-468-1G>C
NM_004020.3:c.-468-1G>C	NP_004011.2:n.-468-1G>C
NM_004020.4:c.-468-1G>C	NP_004011.3:n.-468-1G>C
NM_004021.2:c.-468-1G>C	NP_004012.1:n.-468-1G>C
NM_004021.3:c.-468-1G>C	NP_004012.2:n.-468-1G>C
NM_004022.2:c.-468-1G>C	NP_004013.1:n.-468-1G>C
NM_004022.3:c.-468-1G>C	NP_004013.2:n.-468-1G>C
NM_004023.2:c.-468-1G>C	NP_004014.1:n.-468-1G>C
NM_004023.3:c.-468-1G>C	NP_004014.2:n.-468-1G>C
ENST00000357033.8:c.6913-1G>C	ENSP00000354923.3:n.6913-1G>C
ENST00000358062.7:c.1759-1G>C	ENSP00000350765.3:n.1759-1G>C
ENST00000359836.5:c.-468-1G>C	ENSP00000352894.1:n.-468-1G>C
ENST00000378677.6:c.6901-1G>C	ENSP00000367948.2:n.6901-1G>C
ENST00000378707.7:c.-468-1G>C	ENSP00000367979.3:n.-468-1G>C
ENST00000474231.5:c.-468-1G>C	ENSP00000417123.1:n.-468-1G>C
ENST00000541735.5:c.-468-1G>C	ENSP00000444119.1:n.-468-1G>C
ENST00000619831.4:c.6898-1G>C	ENSP00000479270.1:n.6898-1G>C
ENST00000619831.5:c.2881-1G>C	ENSP00000479270.2:n.2881-1G>C
ENST00000620040.4:c.6910-1G>C	ENSP00000478150.1:n.6910-1G>C
ENST00000620040.5:c.-468-1G>C	ENSP00000478150.2:n.-468-1G>C
ENST00000680961.1:c.-468-1G>C	ENSP00000506386.1:n.-468-1G>C
ENST00000681646.1:n.574-1G>C
ENST00000682238.1:c.-468-1G>C	ENSP00000508124.1:n.-468-1G>C
ENST00000683117.1:n.574-1G>C
ENST00000683450.1:n.496-1G>C
ENST00000683851.1:n.574-1G>C
ENST00000683957.1:n.405-1G>C
ENST00000684130.1:c.-468-1G>C	ENSP00000508037.1:n.-468-1G>C
XM_006724468.2:c.6913-1G>C	XP_006724531.1:n.6913-1G>C
XM_006724469.2:c.6889-1G>C	XP_006724532.1:n.6889-1G>C
XM_006724469.3:c.6889-1G>C	XP_006724532.1:n.6889-1G>C
XM_006724470.2:c.6913-1G>C	XP_006724533.1:n.6913-1G>C
XM_006724470.3:c.6913-1G>C	XP_006724533.1:n.6913-1G>C
XM_006724471.2:c.6913-1G>C	XP_006724534.1:n.6913-1G>C
XM_006724472.2:c.6784-1G>C	XP_006724535.1:n.6784-1G>C
XM_006724473.2:c.6775-1G>C	XP_006724536.1:n.6775-1G>C
XM_006724474.2:c.6913-1G>C	XP_006724537.1:n.6913-1G>C
XM_006724474.3:c.6913-1G>C	XP_006724537.1:n.6913-1G>C
XM_006724475.2:c.6913-1G>C	XP_006724538.1:n.6913-1G>C
XM_011545467.1:c.6790-1G>C	XP_011543769.1:n.6790-1G>C
XM_011545468.1:c.6913-1G>C	XP_011543770.1:n.6913-1G>C
XM_011545468.2:c.6913-1G>C	XP_011543770.1:n.6913-1G>C
XM_017029328.1:c.6913-1G>C	XP_016884817.1:n.6913-1G>C
XM_017029331.1:c.1087-1G>C	XP_016884820.1:n.1087-1G>C