Canonical Allele Identifier: CA2693407107

Gene: DMD

Linked Data

• gnomAD v4: X-32364719-TAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32364721_32364722del , CM000685.2:g.32364721_32364722del	GRCh38
NC_000023.10:g.32382838_32382839del , CM000685.1:g.32382838_32382839del	GRCh37
NC_000023.9:g.32292759_32292760del	NCBI36
NG_012232.1:g.979889_979890del , LRG_199:g.979889_979890del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357033.9:c.5026-11_5026-10del MANE Select	ENSP00000354923.3:n.5026-11_5026-10del
ENST00000619831.5:c.994-11_994-10del	ENSP00000479270.2:n.994-11_994-10del
ENST00000357033.8:c.5026-11_5026-10del	ENSP00000354923.3:n.5026-11_5026-10del
ENST00000378677.6:c.5014-11_5014-10del	ENSP00000367948.2:n.5014-11_5014-10del
ENST00000420596.5:c.274-11_274-10del	ENSP00000399897.1:n.274-11_274-10del
ENST00000448370.5:c.94-11_94-10del	ENSP00000388559.1:n.94-11_94-10del
ENST00000488902.5:n.336-147658_336-147657del
ENST00000619831.4:c.5014-11_5014-10del	ENSP00000479270.1:n.5014-11_5014-10del
ENST00000620040.4:c.5026-11_5026-10del	ENSP00000478150.1:n.5026-11_5026-10del
NM_000109.3:c.5002-11_5002-10del	NP_000100.2:n.5002-11_5002-10del
NM_004006.2:c.5026-11_5026-10del , LRG_199t1:c.5026-11_5026-10del	NP_003997.1:n.5026-11_5026-10del
NM_004009.3:c.5014-11_5014-10del	NP_004000.1:n.5014-11_5014-10del
NM_004010.3:c.4657-11_4657-10del	NP_004001.1:n.4657-11_4657-10del
NM_004011.3:c.1003-11_1003-10del	NP_004002.2:n.1003-11_1003-10del
NM_004012.3:c.994-11_994-10del	NP_004003.1:n.994-11_994-10del
XM_006724468.2:c.5026-11_5026-10del	XP_006724531.1:n.5026-11_5026-10del
XM_006724469.2:c.5002-11_5002-10del	XP_006724532.1:n.5002-11_5002-10del
XM_006724470.2:c.5026-11_5026-10del	XP_006724533.1:n.5026-11_5026-10del
XM_006724471.2:c.5026-11_5026-10del	XP_006724534.1:n.5026-11_5026-10del
XM_006724472.2:c.4897-11_4897-10del	XP_006724535.1:n.4897-11_4897-10del
XM_006724473.2:c.5026-11_5026-10del	XP_006724536.1:n.5026-11_5026-10del
XM_006724474.2:c.5026-11_5026-10del	XP_006724537.1:n.5026-11_5026-10del
XM_006724475.2:c.5026-11_5026-10del	XP_006724538.1:n.5026-11_5026-10del
XM_011545467.1:c.5026-11_5026-10del	XP_011543769.1:n.5026-11_5026-10del
XM_011545468.1:c.5026-11_5026-10del	XP_011543770.1:n.5026-11_5026-10del
XM_011545469.1:c.5026-11_5026-10del	XP_011543771.1:n.5026-11_5026-10del
XM_006724469.3:c.5002-11_5002-10del	XP_006724532.1:n.5002-11_5002-10del
XM_006724470.3:c.5026-11_5026-10del	XP_006724533.1:n.5026-11_5026-10del
XM_006724474.3:c.5026-11_5026-10del	XP_006724537.1:n.5026-11_5026-10del
XM_011545468.2:c.5026-11_5026-10del	XP_011543770.1:n.5026-11_5026-10del
XM_017029328.1:c.5026-11_5026-10del	XP_016884817.1:n.5026-11_5026-10del
XM_017029329.1:c.5026-11_5026-10del	XP_016884818.1:n.5026-11_5026-10del
XM_017029330.2:c.5026-11_5026-10del	XP_016884819.1:n.5026-11_5026-10del
NM_000109.4:c.5002-11_5002-10del	NP_000100.3:n.5002-11_5002-10del
NM_004006.3:c.5026-11_5026-10del MANE Select	NP_003997.2:n.5026-11_5026-10del
NM_004011.4:c.1003-11_1003-10del	NP_004002.3:n.1003-11_1003-10del
NM_004012.4:c.994-11_994-10del	NP_004003.2:n.994-11_994-10del