Canonical Allele Identifier: CA2422736463

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32287681T= , CM000685.2:g.32287681T=	GRCh38
NC_000023.10:g.32305798T= , CM000685.1:g.32305798T=	GRCh37
NC_000023.9:g.32215719T=	NCBI36
NG_012232.1:g.1056929A= , LRG_199:g.1056929A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358062.7:c.984A=	ENSP00000350765.3:p.Gln328=
ENST00000357033.9:c.6138A= MANE Select	ENSP00000354923.3:p.Gln2046=
ENST00000619831.5:c.2106A=	ENSP00000479270.2:p.Gln702=
ENST00000357033.8:c.6138A=	ENSP00000354923.3:p.Gln2046=
ENST00000378677.6:c.6126A=	ENSP00000367948.2:p.Gln2042=
ENST00000488902.5:n.336-70618A=
ENST00000619831.4:c.6126A=	ENSP00000479270.1:p.Gln2042=
ENST00000620040.4:c.6138A=	ENSP00000478150.1:p.Gln2046=
NM_000109.3:c.6114A=	NP_000100.2:p.Gln2038=
NM_004006.2:c.6138A= , LRG_199t1:c.6138A=	NP_003997.1:p.Gln2046=
NM_004009.3:c.6126A=	NP_004000.1:p.Gln2042=
NM_004010.3:c.5769A=	NP_004001.1:p.Gln1923=
NM_004011.3:c.2115A=	NP_004002.2:p.Gln705=
NM_004012.3:c.2106A=	NP_004003.1:p.Gln702=
XM_006724468.2:c.6138A=	XP_006724531.1:p.Gln2046=
XM_006724469.2:c.6114A=	XP_006724532.1:p.Gln2038=
XM_006724470.2:c.6138A=	XP_006724533.1:p.Gln2046=
XM_006724471.2:c.6138A=	XP_006724534.1:p.Gln2046=
XM_006724472.2:c.6009A=	XP_006724535.1:p.Gln2003=
XM_006724473.2:c.6000A=	XP_006724536.1:p.Gln2000=
XM_006724474.2:c.6138A=	XP_006724537.1:p.Gln2046=
XM_006724475.2:c.6138A=	XP_006724538.1:p.Gln2046=
XM_011545467.1:c.6015A=	XP_011543769.1:p.Gln2005=
XM_011545468.1:c.6138A=	XP_011543770.1:p.Gln2046=
XM_006724469.3:c.6114A=	XP_006724532.1:p.Gln2038=
XM_006724470.3:c.6138A=	XP_006724533.1:p.Gln2046=
XM_006724474.3:c.6138A=	XP_006724537.1:p.Gln2046=
XM_011545468.2:c.6138A=	XP_011543770.1:p.Gln2046=
XM_017029328.1:c.6138A=	XP_016884817.1:p.Gln2046=
XM_017029329.1:c.6138A=	XP_016884818.1:p.Gln2046=
XM_017029330.2:c.6138A=	XP_016884819.1:p.Gln2046=
XM_017029331.1:c.312A=	XP_016884820.1:p.Gln104=
NM_000109.4:c.6114A=	NP_000100.3:p.Gln2038=
NM_004006.3:c.6138A= MANE Select	NP_003997.2:p.Gln2046=
NM_004011.4:c.2115A=	NP_004002.3:p.Gln705=
NM_004012.4:c.2106A=	NP_004003.2:p.Gln702=