Canonical Allele Identifier: CA2422770129

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32365109_32365112delinsCCTT , CM000685.2:g.32365109_32365112delinsCCTT	GRCh38
NC_000023.10:g.32383226_32383229delinsCCTT , CM000685.1:g.32383226_32383229delinsCCTT	GRCh37
NC_000023.9:g.32293147_32293150delinsCCTT	NCBI36
NG_012232.1:g.979498_979501delinsAAGG , LRG_199:g.979498_979501delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357033.9:c.4933_4936delinsAAGG MANE Select	ENSP00000354923.3:p.Lys1645=
ENST00000619831.5:c.901_904delinsAAGG	ENSP00000479270.2:p.Lys301=
ENST00000357033.8:c.4933_4936delinsAAGG	ENSP00000354923.3:p.Lys1645=
ENST00000378677.6:c.4921_4924delinsAAGG	ENSP00000367948.2:p.Lys1641=
ENST00000420596.5:c.181_184delinsAAGG	ENSP00000399897.1:p.Lys61=
ENST00000448370.5:c.94-402_94-399delinsAAGG	ENSP00000388559.1:n.94-402_94-399delinsAAGG
ENST00000488902.5:n.336-148049_336-148046delinsAAGG
ENST00000619831.4:c.4921_4924delinsAAGG	ENSP00000479270.1:p.Lys1641=
ENST00000620040.4:c.4933_4936delinsAAGG	ENSP00000478150.1:p.Lys1645=
NM_000109.3:c.4909_4912delinsAAGG	NP_000100.2:p.Lys1637=
NM_004006.2:c.4933_4936delinsAAGG , LRG_199t1:c.4933_4936delinsAAGG	NP_003997.1:p.Lys1645=
NM_004009.3:c.4921_4924delinsAAGG	NP_004000.1:p.Lys1641=
NM_004010.3:c.4564_4567delinsAAGG	NP_004001.1:p.Lys1522=
NM_004011.3:c.910_913delinsAAGG	NP_004002.2:p.Lys304=
NM_004012.3:c.901_904delinsAAGG	NP_004003.1:p.Lys301=
XM_006724468.2:c.4933_4936delinsAAGG	XP_006724531.1:p.Lys1645=
XM_006724469.2:c.4909_4912delinsAAGG	XP_006724532.1:p.Lys1637=
XM_006724470.2:c.4933_4936delinsAAGG	XP_006724533.1:p.Lys1645=
XM_006724471.2:c.4933_4936delinsAAGG	XP_006724534.1:p.Lys1645=
XM_006724472.2:c.4804_4807delinsAAGG	XP_006724535.1:p.Lys1602=
XM_006724473.2:c.4933_4936delinsAAGG	XP_006724536.1:p.Lys1645=
XM_006724474.2:c.4933_4936delinsAAGG	XP_006724537.1:p.Lys1645=
XM_006724475.2:c.4933_4936delinsAAGG	XP_006724538.1:p.Lys1645=
XM_011545467.1:c.4933_4936delinsAAGG	XP_011543769.1:p.Lys1645=
XM_011545468.1:c.4933_4936delinsAAGG	XP_011543770.1:p.Lys1645=
XM_011545469.1:c.4933_4936delinsAAGG	XP_011543771.1:p.Lys1645=
XM_006724469.3:c.4909_4912delinsAAGG	XP_006724532.1:p.Lys1637=
XM_006724470.3:c.4933_4936delinsAAGG	XP_006724533.1:p.Lys1645=
XM_006724474.3:c.4933_4936delinsAAGG	XP_006724537.1:p.Lys1645=
XM_011545468.2:c.4933_4936delinsAAGG	XP_011543770.1:p.Lys1645=
XM_017029328.1:c.4933_4936delinsAAGG	XP_016884817.1:p.Lys1645=
XM_017029329.1:c.4933_4936delinsAAGG	XP_016884818.1:p.Lys1645=
XM_017029330.2:c.4933_4936delinsAAGG	XP_016884819.1:p.Lys1645=
NM_000109.4:c.4909_4912delinsAAGG	NP_000100.3:p.Lys1637=
NM_004006.3:c.4933_4936delinsAAGG MANE Select	NP_003997.2:p.Lys1645=
NM_004011.4:c.910_913delinsAAGG	NP_004002.3:p.Lys304=
NM_004012.4:c.901_904delinsAAGG	NP_004003.2:p.Lys301=