Canonical Allele Identifier: CA412655226

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.31462692T>G (hg19) ; chrX:g.31444575T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31444575T>G , CM000685.2:g.31444575T>G	GRCh38
NC_000023.10:g.31462692T>G , CM000685.1:g.31462692T>G	GRCh37
NC_000023.9:g.31372613T>G	NCBI36
NG_012232.1:g.1900035A>C , LRG_199:g.1900035A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.3836A>C	ENSP00000350765.3:p.Asp1279Ala
ENST00000682238.1:c.1610A>C	ENSP00000508124.1:p.Asp537Ala
ENST00000683450.1:n.2455A>C
ENST00000683957.1:n.2482A>C
ENST00000684130.1:c.1610A>C	ENSP00000508037.1:p.Asp537Ala
ENST00000343523.7:c.845A>C	ENSP00000340057.4:p.Asp282Ala
ENST00000357033.9:c.8990A>C MANE Select	ENSP00000354923.3:p.Asp2997Ala
ENST00000619831.5:c.4958A>C	ENSP00000479270.2:p.Asp1653Ala
ENST00000620040.5:c.1610A>C	ENSP00000478150.2:p.Asp537Ala
ENST00000680961.1:c.1610A>C	ENSP00000506386.1:p.Asp537Ala
ENST00000681646.1:n.2651A>C
ENST00000343523.6:c.803A>C	ENSP00000340057.3:p.Asp268Ala
ENST00000357033.8:c.8990A>C	ENSP00000354923.3:p.Asp2997Ala
ENST00000358062.6:c.2078A>C	ENSP00000350765.2:p.Asp693Ala
ENST00000359836.5:c.1610A>C	ENSP00000352894.1:p.Asp537Ala
ENST00000378677.6:c.8978A>C	ENSP00000367948.2:p.Asp2993Ala
ENST00000378707.7:c.1610A>C	ENSP00000367979.3:p.Asp537Ala
ENST00000474231.5:c.1610A>C	ENSP00000417123.1:p.Asp537Ala
ENST00000541735.5:c.1610A>C	ENSP00000444119.1:p.Asp537Ala
ENST00000619831.4:c.8975A>C	ENSP00000479270.1:p.Asp2992Ala
ENST00000620040.4:c.8987A>C	ENSP00000478150.1:p.Asp2996Ala
NM_000109.3:c.8966A>C	NP_000100.2:p.Asp2989Ala
NM_004006.2:c.8990A>C , LRG_199t1:c.8990A>C	NP_003997.1:p.Asp2997Ala
NM_004009.3:c.8978A>C	NP_004000.1:p.Asp2993Ala
NM_004010.3:c.8621A>C	NP_004001.1:p.Asp2874Ala
NM_004011.3:c.4967A>C	NP_004002.2:p.Asp1656Ala
NM_004012.3:c.4958A>C	NP_004003.1:p.Asp1653Ala
NM_004013.2:c.1610A>C	NP_004004.1:p.Asp537Ala
NM_004014.2:c.803A>C	NP_004005.1:p.Asp268Ala
NM_004020.3:c.1610A>C	NP_004011.2:p.Asp537Ala
NM_004021.2:c.1610A>C	NP_004012.1:p.Asp537Ala
NM_004022.2:c.1610A>C	NP_004013.1:p.Asp537Ala
NM_004023.2:c.1610A>C	NP_004014.1:p.Asp537Ala
XM_006724468.2:c.8990A>C	XP_006724531.1:p.Asp2997Ala
XM_006724469.2:c.8966A>C	XP_006724532.1:p.Asp2989Ala
XM_006724470.2:c.8990A>C	XP_006724533.1:p.Asp2997Ala
XM_006724471.2:c.8990A>C	XP_006724534.1:p.Asp2997Ala
XM_006724472.2:c.8861A>C	XP_006724535.1:p.Asp2954Ala
XM_006724473.2:c.8852A>C	XP_006724536.1:p.Asp2951Ala
XM_006724474.2:c.8990A>C	XP_006724537.1:p.Asp2997Ala
XM_006724475.2:c.8990A>C	XP_006724538.1:p.Asp2997Ala
XM_011545467.1:c.8867A>C	XP_011543769.1:p.Asp2956Ala
XM_011545468.1:c.8990A>C	XP_011543770.1:p.Asp2997Ala
XM_006724469.3:c.8966A>C	XP_006724532.1:p.Asp2989Ala
XM_006724470.3:c.8990A>C	XP_006724533.1:p.Asp2997Ala
XM_006724474.3:c.8990A>C	XP_006724537.1:p.Asp2997Ala
XM_011545468.2:c.8990A>C	XP_011543770.1:p.Asp2997Ala
XM_017029328.1:c.8990A>C	XP_016884817.1:p.Asp2997Ala
XM_017029331.1:c.3164A>C	XP_016884820.1:p.Asp1055Ala
NM_000109.4:c.8966A>C	NP_000100.3:p.Asp2989Ala
NM_004006.3:c.8990A>C MANE Select	NP_003997.2:p.Asp2997Ala
NM_004011.4:c.4967A>C	NP_004002.3:p.Asp1656Ala
NM_004012.4:c.4958A>C	NP_004003.2:p.Asp1653Ala
NM_004021.3:c.1610A>C	NP_004012.2:p.Asp537Ala
NM_004023.3:c.1610A>C	NP_004014.2:p.Asp537Ala
NM_004013.3:c.1610A>C	NP_004004.2:p.Asp537Ala
NM_004014.3:c.803A>C	NP_004005.2:p.Asp268Ala
NM_004020.4:c.1610A>C	NP_004011.3:p.Asp537Ala
NM_004022.3:c.1610A>C	NP_004013.2:p.Asp537Ala