Canonical Allele Identifier: CA412672665

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32365200C>A , CM000685.2:g.32365200C>A	GRCh38
NC_000023.10:g.32383317C>A , CM000685.1:g.32383317C>A	GRCh37
NC_000023.9:g.32293238C>A	NCBI36
NG_012232.1:g.979410G>T , LRG_199:g.979410G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004006.3:c.4846-1G>T MANE Select	NP_003997.2:n.4846-1G>T
ENST00000357033.9:c.4846-1G>T MANE Select	ENSP00000354923.3:n.4846-1G>T
NM_000109.3:c.4822-1G>T	NP_000100.2:n.4822-1G>T
NM_000109.4:c.4822-1G>T	NP_000100.3:n.4822-1G>T
NM_004006.2:c.4846-1G>T , LRG_199t1:c.4846-1G>T	NP_003997.1:n.4846-1G>T
NM_004009.3:c.4834-1G>T	NP_004000.1:n.4834-1G>T
NM_004010.3:c.4477-1G>T	NP_004001.1:n.4477-1G>T
NM_004011.3:c.823-1G>T	NP_004002.2:n.823-1G>T
NM_004011.4:c.823-1G>T	NP_004002.3:n.823-1G>T
NM_004012.3:c.814-1G>T	NP_004003.1:n.814-1G>T
NM_004012.4:c.814-1G>T	NP_004003.2:n.814-1G>T
ENST00000357033.8:c.4846-1G>T	ENSP00000354923.3:n.4846-1G>T
ENST00000378677.6:c.4834-1G>T	ENSP00000367948.2:n.4834-1G>T
ENST00000420596.5:c.94-1G>T	ENSP00000399897.1:n.94-1G>T
ENST00000448370.5:c.94-490G>T	ENSP00000388559.1:n.94-490G>T
ENST00000488902.5:n.336-148137G>T
ENST00000619831.4:c.4834-1G>T	ENSP00000479270.1:n.4834-1G>T
ENST00000619831.5:c.814-1G>T	ENSP00000479270.2:n.814-1G>T
ENST00000620040.4:c.4846-1G>T	ENSP00000478150.1:n.4846-1G>T
XM_006724468.2:c.4846-1G>T	XP_006724531.1:n.4846-1G>T
XM_006724469.2:c.4822-1G>T	XP_006724532.1:n.4822-1G>T
XM_006724469.3:c.4822-1G>T	XP_006724532.1:n.4822-1G>T
XM_006724470.2:c.4846-1G>T	XP_006724533.1:n.4846-1G>T
XM_006724470.3:c.4846-1G>T	XP_006724533.1:n.4846-1G>T
XM_006724471.2:c.4846-1G>T	XP_006724534.1:n.4846-1G>T
XM_006724472.2:c.4717-1G>T	XP_006724535.1:n.4717-1G>T
XM_006724473.2:c.4846-1G>T	XP_006724536.1:n.4846-1G>T
XM_006724474.2:c.4846-1G>T	XP_006724537.1:n.4846-1G>T
XM_006724474.3:c.4846-1G>T	XP_006724537.1:n.4846-1G>T
XM_006724475.2:c.4846-1G>T	XP_006724538.1:n.4846-1G>T
XM_011545467.1:c.4846-1G>T	XP_011543769.1:n.4846-1G>T
XM_011545468.1:c.4846-1G>T	XP_011543770.1:n.4846-1G>T
XM_011545468.2:c.4846-1G>T	XP_011543770.1:n.4846-1G>T
XM_011545469.1:c.4846-1G>T	XP_011543771.1:n.4846-1G>T
XM_017029328.1:c.4846-1G>T	XP_016884817.1:n.4846-1G>T
XM_017029329.1:c.4846-1G>T	XP_016884818.1:n.4846-1G>T
XM_017029330.2:c.4846-1G>T	XP_016884819.1:n.4846-1G>T