Canonical Allele Identifier: CA2422770026

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32364882A= , CM000685.2:g.32364882A=	GRCh38
NC_000023.10:g.32382999A= , CM000685.1:g.32382999A=	GRCh37
NC_000023.9:g.32292920A=	NCBI36
NG_012232.1:g.979728T= , LRG_199:g.979728T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357033.9:c.5025+138T= MANE Select	ENSP00000354923.3:n.5025+138T=
ENST00000619831.5:c.993+138T=	ENSP00000479270.2:n.993+138T=
ENST00000357033.8:c.5025+138T=	ENSP00000354923.3:n.5025+138T=
ENST00000378677.6:c.5013+138T=	ENSP00000367948.2:n.5013+138T=
ENST00000420596.5:c.273+138T=	ENSP00000399897.1:n.273+138T=
ENST00000448370.5:c.94-172T=	ENSP00000388559.1:n.94-172T=
ENST00000488902.5:n.336-147819T=
ENST00000619831.4:c.5013+138T=	ENSP00000479270.1:n.5013+138T=
ENST00000620040.4:c.5025+138T=	ENSP00000478150.1:n.5025+138T=
NM_000109.3:c.5001+138T=	NP_000100.2:n.5001+138T=
NM_004006.2:c.5025+138T= , LRG_199t1:c.5025+138T=	NP_003997.1:n.5025+138T=
NM_004009.3:c.5013+138T=	NP_004000.1:n.5013+138T=
NM_004010.3:c.4656+138T=	NP_004001.1:n.4656+138T=
NM_004011.3:c.1002+138T=	NP_004002.2:n.1002+138T=
NM_004012.3:c.993+138T=	NP_004003.1:n.993+138T=
XM_006724468.2:c.5025+138T=	XP_006724531.1:n.5025+138T=
XM_006724469.2:c.5001+138T=	XP_006724532.1:n.5001+138T=
XM_006724470.2:c.5025+138T=	XP_006724533.1:n.5025+138T=
XM_006724471.2:c.5025+138T=	XP_006724534.1:n.5025+138T=
XM_006724472.2:c.4896+138T=	XP_006724535.1:n.4896+138T=
XM_006724473.2:c.5025+138T=	XP_006724536.1:n.5025+138T=
XM_006724474.2:c.5025+138T=	XP_006724537.1:n.5025+138T=
XM_006724475.2:c.5025+138T=	XP_006724538.1:n.5025+138T=
XM_011545467.1:c.5025+138T=	XP_011543769.1:n.5025+138T=
XM_011545468.1:c.5025+138T=	XP_011543770.1:n.5025+138T=
XM_011545469.1:c.5025+138T=	XP_011543771.1:n.5025+138T=
XM_006724469.3:c.5001+138T=	XP_006724532.1:n.5001+138T=
XM_006724470.3:c.5025+138T=	XP_006724533.1:n.5025+138T=
XM_006724474.3:c.5025+138T=	XP_006724537.1:n.5025+138T=
XM_011545468.2:c.5025+138T=	XP_011543770.1:n.5025+138T=
XM_017029328.1:c.5025+138T=	XP_016884817.1:n.5025+138T=
XM_017029329.1:c.5025+138T=	XP_016884818.1:n.5025+138T=
XM_017029330.2:c.5025+138T=	XP_016884819.1:n.5025+138T=
NM_000109.4:c.5001+138T=	NP_000100.3:n.5001+138T=
NM_004006.3:c.5025+138T= MANE Select	NP_003997.2:n.5025+138T=
NM_004011.4:c.1002+138T=	NP_004002.3:n.1002+138T=
NM_004012.4:c.993+138T=	NP_004003.2:n.993+138T=