Canonical Allele Identifier: CA412660969

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32380523A>T , CM000685.2:g.32380523A>T	GRCh38
NC_000023.10:g.32398640A>T , CM000685.1:g.32398640A>T	GRCh37
NC_000023.9:g.32308561A>T	NCBI36
NG_012232.1:g.964087T>A , LRG_199:g.964087T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004006.3:c.4832T>A MANE Select	NP_003997.2:p.Val1611Asp
ENST00000357033.9:c.4832T>A MANE Select	ENSP00000354923.3:p.Val1611Asp
NM_000109.3:c.4808T>A	NP_000100.2:p.Val1603Asp
NM_000109.4:c.4808T>A	NP_000100.3:p.Val1603Asp
NM_004006.2:c.4832T>A , LRG_199t1:c.4832T>A	NP_003997.1:p.Val1611Asp
NM_004009.3:c.4820T>A	NP_004000.1:p.Val1607Asp
NM_004010.3:c.4463T>A	NP_004001.1:p.Val1488Asp
NM_004011.3:c.809T>A	NP_004002.2:p.Val270Asp
NM_004011.4:c.809T>A	NP_004002.3:p.Val270Asp
NM_004012.3:c.800T>A	NP_004003.1:p.Val267Asp
NM_004012.4:c.800T>A	NP_004003.2:p.Val267Asp
ENST00000357033.8:c.4832T>A	ENSP00000354923.3:p.Val1611Asp
ENST00000378677.6:c.4820T>A	ENSP00000367948.2:p.Val1607Asp
ENST00000420596.5:c.94-15324T>A	ENSP00000399897.1:n.94-15324T>A
ENST00000448370.5:c.94-15813T>A	ENSP00000388559.1:n.94-15813T>A
ENST00000488902.5:n.336-163460T>A
ENST00000619831.4:c.4820T>A	ENSP00000479270.1:p.Val1607Asp
ENST00000619831.5:c.800T>A	ENSP00000479270.2:p.Val267Asp
ENST00000620040.4:c.4832T>A	ENSP00000478150.1:p.Val1611Asp
XM_006724468.2:c.4832T>A	XP_006724531.1:p.Val1611Asp
XM_006724469.2:c.4808T>A	XP_006724532.1:p.Val1603Asp
XM_006724469.3:c.4808T>A	XP_006724532.1:p.Val1603Asp
XM_006724470.2:c.4832T>A	XP_006724533.1:p.Val1611Asp
XM_006724470.3:c.4832T>A	XP_006724533.1:p.Val1611Asp
XM_006724471.2:c.4832T>A	XP_006724534.1:p.Val1611Asp
XM_006724472.2:c.4703T>A	XP_006724535.1:p.Val1568Asp
XM_006724473.2:c.4832T>A	XP_006724536.1:p.Val1611Asp
XM_006724474.2:c.4832T>A	XP_006724537.1:p.Val1611Asp
XM_006724474.3:c.4832T>A	XP_006724537.1:p.Val1611Asp
XM_006724475.2:c.4832T>A	XP_006724538.1:p.Val1611Asp
XM_011545467.1:c.4832T>A	XP_011543769.1:p.Val1611Asp
XM_011545468.1:c.4832T>A	XP_011543770.1:p.Val1611Asp
XM_011545468.2:c.4832T>A	XP_011543770.1:p.Val1611Asp
XM_011545469.1:c.4832T>A	XP_011543771.1:p.Val1611Asp
XM_017029328.1:c.4832T>A	XP_016884817.1:p.Val1611Asp
XM_017029329.1:c.4832T>A	XP_016884818.1:p.Val1611Asp
XM_017029330.2:c.4832T>A	XP_016884819.1:p.Val1611Asp