Canonical Allele Identifier: CA412666354

Gene: DMD

Linked Data

• gnomAD v4: X-32287655-A-G
• MyVariant Identifiers: chrX:g.32305772A>G (hg19) ; chrX:g.32287655A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32287655A>G , CM000685.2:g.32287655A>G	GRCh38
NC_000023.10:g.32305772A>G , CM000685.1:g.32305772A>G	GRCh37
NC_000023.9:g.32215693A>G	NCBI36
NG_012232.1:g.1056955T>C , LRG_199:g.1056955T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.1010T>C	ENSP00000350765.3:p.Ile337Thr
ENST00000357033.9:c.6164T>C MANE Select	ENSP00000354923.3:p.Ile2055Thr
ENST00000619831.5:c.2132T>C	ENSP00000479270.2:p.Ile711Thr
ENST00000357033.8:c.6164T>C	ENSP00000354923.3:p.Ile2055Thr
ENST00000378677.6:c.6152T>C	ENSP00000367948.2:p.Ile2051Thr
ENST00000488902.5:n.336-70592T>C
ENST00000619831.4:c.6152T>C	ENSP00000479270.1:p.Ile2051Thr
ENST00000620040.4:c.6164T>C	ENSP00000478150.1:p.Ile2055Thr
NM_000109.3:c.6140T>C	NP_000100.2:p.Ile2047Thr
NM_004006.2:c.6164T>C , LRG_199t1:c.6164T>C	NP_003997.1:p.Ile2055Thr
NM_004009.3:c.6152T>C	NP_004000.1:p.Ile2051Thr
NM_004010.3:c.5795T>C	NP_004001.1:p.Ile1932Thr
NM_004011.3:c.2141T>C	NP_004002.2:p.Ile714Thr
NM_004012.3:c.2132T>C	NP_004003.1:p.Ile711Thr
XM_006724468.2:c.6164T>C	XP_006724531.1:p.Ile2055Thr
XM_006724469.2:c.6140T>C	XP_006724532.1:p.Ile2047Thr
XM_006724470.2:c.6164T>C	XP_006724533.1:p.Ile2055Thr
XM_006724471.2:c.6164T>C	XP_006724534.1:p.Ile2055Thr
XM_006724472.2:c.6035T>C	XP_006724535.1:p.Ile2012Thr
XM_006724473.2:c.6026T>C	XP_006724536.1:p.Ile2009Thr
XM_006724474.2:c.6164T>C	XP_006724537.1:p.Ile2055Thr
XM_006724475.2:c.6164T>C	XP_006724538.1:p.Ile2055Thr
XM_011545467.1:c.6041T>C	XP_011543769.1:p.Ile2014Thr
XM_011545468.1:c.6164T>C	XP_011543770.1:p.Ile2055Thr
XM_006724469.3:c.6140T>C	XP_006724532.1:p.Ile2047Thr
XM_006724470.3:c.6164T>C	XP_006724533.1:p.Ile2055Thr
XM_006724474.3:c.6164T>C	XP_006724537.1:p.Ile2055Thr
XM_011545468.2:c.6164T>C	XP_011543770.1:p.Ile2055Thr
XM_017029328.1:c.6164T>C	XP_016884817.1:p.Ile2055Thr
XM_017029329.1:c.6164T>C	XP_016884818.1:p.Ile2055Thr
XM_017029330.2:c.6164T>C	XP_016884819.1:p.Ile2055Thr
XM_017029331.1:c.338T>C	XP_016884820.1:p.Ile113Thr
NM_000109.4:c.6140T>C	NP_000100.3:p.Ile2047Thr
NM_004006.3:c.6164T>C MANE Select	NP_003997.2:p.Ile2055Thr
NM_004011.4:c.2141T>C	NP_004002.3:p.Ile714Thr
NM_004012.4:c.2132T>C	NP_004003.2:p.Ile711Thr