Canonical Allele Identifier: CA267150

Gene: DMD

Linked Data

• ClinVar Variation Id: 94781
• ClinVar RCV Id: RCV000080774 ; RCV001854425
• dbSNP Id: rs398124058
• MyVariant Identifiers: chrX:g.31676240G>A (hg19) ; chrX:g.31658123G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31658123G>A , CM000685.2:g.31658123G>A	GRCh38
NC_000023.10:g.31676240G>A , CM000685.1:g.31676240G>A	GRCh37
NC_000023.9:g.31586161G>A	NCBI36
NG_012232.1:g.1686487C>T , LRG_199:g.1686487C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.2740C>T	ENSP00000350765.3:p.Gln914Ter
ENST00000682238.1:c.514C>T	ENSP00000508124.1:p.Gln172Ter
ENST00000683450.1:n.1359C>T
ENST00000683851.1:n.1555C>T
ENST00000683957.1:n.1386C>T
ENST00000684130.1:c.514C>T	ENSP00000508037.1:p.Gln172Ter
ENST00000357033.9:c.7894C>T MANE Select	ENSP00000354923.3:p.Gln2632Ter
ENST00000619831.5:c.3862C>T	ENSP00000479270.2:p.Gln1288Ter
ENST00000620040.5:c.514C>T	ENSP00000478150.2:p.Gln172Ter
ENST00000680961.1:c.514C>T	ENSP00000506386.1:p.Gln172Ter
ENST00000681646.1:n.1555C>T
ENST00000357033.8:c.7894C>T	ENSP00000354923.3:p.Gln2632Ter
ENST00000358062.6:c.982C>T	ENSP00000350765.2:p.Gln328Ter
ENST00000359836.5:c.514C>T	ENSP00000352894.1:p.Gln172Ter
ENST00000378677.6:c.7882C>T	ENSP00000367948.2:p.Gln2628Ter
ENST00000378707.7:c.514C>T	ENSP00000367979.3:p.Gln172Ter
ENST00000474231.5:c.514C>T	ENSP00000417123.1:p.Gln172Ter
ENST00000541735.5:c.514C>T	ENSP00000444119.1:p.Gln172Ter
ENST00000619831.4:c.7879C>T	ENSP00000479270.1:p.Gln2627Ter
ENST00000620040.4:c.7891C>T	ENSP00000478150.1:p.Gln2631Ter
NM_000109.3:c.7870C>T	NP_000100.2:p.Gln2624Ter
NM_004006.2:c.7894C>T , LRG_199t1:c.7894C>T	NP_003997.1:p.Gln2632Ter
NM_004009.3:c.7882C>T	NP_004000.1:p.Gln2628Ter
NM_004010.3:c.7525C>T	NP_004001.1:p.Gln2509Ter
NM_004011.3:c.3871C>T	NP_004002.2:p.Gln1291Ter
NM_004012.3:c.3862C>T	NP_004003.1:p.Gln1288Ter
NM_004013.2:c.514C>T	NP_004004.1:p.Gln172Ter
NM_004020.3:c.514C>T	NP_004011.2:p.Gln172Ter
NM_004021.2:c.514C>T	NP_004012.1:p.Gln172Ter
NM_004022.2:c.514C>T	NP_004013.1:p.Gln172Ter
NM_004023.2:c.514C>T	NP_004014.1:p.Gln172Ter
XM_006724468.2:c.7894C>T	XP_006724531.1:p.Gln2632Ter
XM_006724469.2:c.7870C>T	XP_006724532.1:p.Gln2624Ter
XM_006724470.2:c.7894C>T	XP_006724533.1:p.Gln2632Ter
XM_006724471.2:c.7894C>T	XP_006724534.1:p.Gln2632Ter
XM_006724472.2:c.7765C>T	XP_006724535.1:p.Gln2589Ter
XM_006724473.2:c.7756C>T	XP_006724536.1:p.Gln2586Ter
XM_006724474.2:c.7894C>T	XP_006724537.1:p.Gln2632Ter
XM_006724475.2:c.7894C>T	XP_006724538.1:p.Gln2632Ter
XM_011545467.1:c.7771C>T	XP_011543769.1:p.Gln2591Ter
XM_011545468.1:c.7894C>T	XP_011543770.1:p.Gln2632Ter
XM_006724469.3:c.7870C>T	XP_006724532.1:p.Gln2624Ter
XM_006724470.3:c.7894C>T	XP_006724533.1:p.Gln2632Ter
XM_006724474.3:c.7894C>T	XP_006724537.1:p.Gln2632Ter
XM_011545468.2:c.7894C>T	XP_011543770.1:p.Gln2632Ter
XM_017029328.1:c.7894C>T	XP_016884817.1:p.Gln2632Ter
XM_017029331.1:c.2068C>T	XP_016884820.1:p.Gln690Ter
NM_000109.4:c.7870C>T	NP_000100.3:p.Gln2624Ter
NM_004006.3:c.7894C>T MANE Select	NP_003997.2:p.Gln2632Ter
NM_004011.4:c.3871C>T	NP_004002.3:p.Gln1291Ter
NM_004012.4:c.3862C>T	NP_004003.2:p.Gln1288Ter
NM_004021.3:c.514C>T	NP_004012.2:p.Gln172Ter
NM_004023.3:c.514C>T	NP_004014.2:p.Gln172Ter
NM_004013.3:c.514C>T	NP_004004.2:p.Gln172Ter
NM_004020.4:c.514C>T	NP_004011.3:p.Gln172Ter
NM_004022.3:c.514C>T	NP_004013.2:p.Gln172Ter