Canonical Allele Identifier: CA412655142

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.31462651G>C (hg19) ; chrX:g.31444534G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31444534G>C , CM000685.2:g.31444534G>C	GRCh38
NC_000023.10:g.31462651G>C , CM000685.1:g.31462651G>C	GRCh37
NC_000023.9:g.31372572G>C	NCBI36
NG_012232.1:g.1900076C>G , LRG_199:g.1900076C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.3877C>G	ENSP00000350765.3:p.Pro1293Ala
ENST00000682238.1:c.1651C>G	ENSP00000508124.1:p.Pro551Ala
ENST00000683450.1:n.2496C>G
ENST00000683957.1:n.2523C>G
ENST00000684130.1:c.1651C>G	ENSP00000508037.1:p.Pro551Ala
ENST00000343523.7:c.886C>G	ENSP00000340057.4:p.Pro296Ala
ENST00000357033.9:c.9031C>G MANE Select	ENSP00000354923.3:p.Pro3011Ala
ENST00000619831.5:c.4999C>G	ENSP00000479270.2:p.Pro1667Ala
ENST00000620040.5:c.1651C>G	ENSP00000478150.2:p.Pro551Ala
ENST00000680961.1:c.1651C>G	ENSP00000506386.1:p.Pro551Ala
ENST00000681646.1:n.2692C>G
ENST00000343523.6:c.844C>G	ENSP00000340057.3:p.Pro282Ala
ENST00000357033.8:c.9031C>G	ENSP00000354923.3:p.Pro3011Ala
ENST00000358062.6:c.2119C>G	ENSP00000350765.2:p.Pro707Ala
ENST00000359836.5:c.1651C>G	ENSP00000352894.1:p.Pro551Ala
ENST00000378677.6:c.9019C>G	ENSP00000367948.2:p.Pro3007Ala
ENST00000378707.7:c.1651C>G	ENSP00000367979.3:p.Pro551Ala
ENST00000474231.5:c.1651C>G	ENSP00000417123.1:p.Pro551Ala
ENST00000541735.5:c.1651C>G	ENSP00000444119.1:p.Pro551Ala
ENST00000619831.4:c.9016C>G	ENSP00000479270.1:p.Pro3006Ala
ENST00000620040.4:c.9028C>G	ENSP00000478150.1:p.Pro3010Ala
NM_000109.3:c.9007C>G	NP_000100.2:p.Pro3003Ala
NM_004006.2:c.9031C>G , LRG_199t1:c.9031C>G	NP_003997.1:p.Pro3011Ala
NM_004009.3:c.9019C>G	NP_004000.1:p.Pro3007Ala
NM_004010.3:c.8662C>G	NP_004001.1:p.Pro2888Ala
NM_004011.3:c.5008C>G	NP_004002.2:p.Pro1670Ala
NM_004012.3:c.4999C>G	NP_004003.1:p.Pro1667Ala
NM_004013.2:c.1651C>G	NP_004004.1:p.Pro551Ala
NM_004014.2:c.844C>G	NP_004005.1:p.Pro282Ala
NM_004020.3:c.1651C>G	NP_004011.2:p.Pro551Ala
NM_004021.2:c.1651C>G	NP_004012.1:p.Pro551Ala
NM_004022.2:c.1651C>G	NP_004013.1:p.Pro551Ala
NM_004023.2:c.1651C>G	NP_004014.1:p.Pro551Ala
XM_006724468.2:c.9031C>G	XP_006724531.1:p.Pro3011Ala
XM_006724469.2:c.9007C>G	XP_006724532.1:p.Pro3003Ala
XM_006724470.2:c.9031C>G	XP_006724533.1:p.Pro3011Ala
XM_006724471.2:c.9031C>G	XP_006724534.1:p.Pro3011Ala
XM_006724472.2:c.8902C>G	XP_006724535.1:p.Pro2968Ala
XM_006724473.2:c.8893C>G	XP_006724536.1:p.Pro2965Ala
XM_006724474.2:c.9031C>G	XP_006724537.1:p.Pro3011Ala
XM_006724475.2:c.9031C>G	XP_006724538.1:p.Pro3011Ala
XM_011545467.1:c.8908C>G	XP_011543769.1:p.Pro2970Ala
XM_011545468.1:c.9031C>G	XP_011543770.1:p.Pro3011Ala
XM_006724469.3:c.9007C>G	XP_006724532.1:p.Pro3003Ala
XM_006724470.3:c.9031C>G	XP_006724533.1:p.Pro3011Ala
XM_006724474.3:c.9031C>G	XP_006724537.1:p.Pro3011Ala
XM_011545468.2:c.9031C>G	XP_011543770.1:p.Pro3011Ala
XM_017029328.1:c.9031C>G	XP_016884817.1:p.Pro3011Ala
XM_017029331.1:c.3205C>G	XP_016884820.1:p.Pro1069Ala
NM_000109.4:c.9007C>G	NP_000100.3:p.Pro3003Ala
NM_004006.3:c.9031C>G MANE Select	NP_003997.2:p.Pro3011Ala
NM_004011.4:c.5008C>G	NP_004002.3:p.Pro1670Ala
NM_004012.4:c.4999C>G	NP_004003.2:p.Pro1667Ala
NM_004021.3:c.1651C>G	NP_004012.2:p.Pro551Ala
NM_004023.3:c.1651C>G	NP_004014.2:p.Pro551Ala
NM_004013.3:c.1651C>G	NP_004004.2:p.Pro551Ala
NM_004014.3:c.844C>G	NP_004005.2:p.Pro282Ala
NM_004020.4:c.1651C>G	NP_004011.3:p.Pro551Ala
NM_004022.3:c.1651C>G	NP_004013.2:p.Pro551Ala