Canonical Allele Identifier: CA515858334

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.31462742T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31444625T>A , CM000685.2:g.31444625T>A	GRCh38
NC_000023.10:g.31462742T>A , CM000685.1:g.31462742T>A	GRCh37
NC_000023.9:g.31372663T>A	NCBI36
NG_012232.1:g.1899985A>T , LRG_199:g.1899985A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.3786A>T	ENSP00000350765.3:p.Ala1262=
ENST00000682238.1:c.1560A>T	ENSP00000508124.1:p.Ala520=
ENST00000683450.1:n.2405A>T
ENST00000683957.1:n.2432A>T
ENST00000684130.1:c.1560A>T	ENSP00000508037.1:p.Ala520=
ENST00000343523.7:c.795A>T	ENSP00000340057.4:p.Ala265=
ENST00000357033.9:c.8940A>T MANE Select	ENSP00000354923.3:p.Ala2980=
ENST00000619831.5:c.4908A>T	ENSP00000479270.2:p.Ala1636=
ENST00000620040.5:c.1560A>T	ENSP00000478150.2:p.Ala520=
ENST00000680961.1:c.1560A>T	ENSP00000506386.1:p.Ala520=
ENST00000681646.1:n.2601A>T
ENST00000343523.6:c.753A>T	ENSP00000340057.3:p.Ala251=
ENST00000357033.8:c.8940A>T	ENSP00000354923.3:p.Ala2980=
ENST00000358062.6:c.2028A>T	ENSP00000350765.2:p.Ala676=
ENST00000359836.5:c.1560A>T	ENSP00000352894.1:p.Ala520=
ENST00000378677.6:c.8928A>T	ENSP00000367948.2:p.Ala2976=
ENST00000378707.7:c.1560A>T	ENSP00000367979.3:p.Ala520=
ENST00000474231.5:c.1560A>T	ENSP00000417123.1:p.Ala520=
ENST00000541735.5:c.1560A>T	ENSP00000444119.1:p.Ala520=
ENST00000619831.4:c.8925A>T	ENSP00000479270.1:p.Ala2975=
ENST00000620040.4:c.8937A>T	ENSP00000478150.1:p.Ala2979=
NM_000109.3:c.8916A>T	NP_000100.2:p.Ala2972=
NM_004006.2:c.8940A>T , LRG_199t1:c.8940A>T	NP_003997.1:p.Ala2980=
NM_004009.3:c.8928A>T	NP_004000.1:p.Ala2976=
NM_004010.3:c.8571A>T	NP_004001.1:p.Ala2857=
NM_004011.3:c.4917A>T	NP_004002.2:p.Ala1639=
NM_004012.3:c.4908A>T	NP_004003.1:p.Ala1636=
NM_004013.2:c.1560A>T	NP_004004.1:p.Ala520=
NM_004014.2:c.753A>T	NP_004005.1:p.Ala251=
NM_004020.3:c.1560A>T	NP_004011.2:p.Ala520=
NM_004021.2:c.1560A>T	NP_004012.1:p.Ala520=
NM_004022.2:c.1560A>T	NP_004013.1:p.Ala520=
NM_004023.2:c.1560A>T	NP_004014.1:p.Ala520=
XM_006724468.2:c.8940A>T	XP_006724531.1:p.Ala2980=
XM_006724469.2:c.8916A>T	XP_006724532.1:p.Ala2972=
XM_006724470.2:c.8940A>T	XP_006724533.1:p.Ala2980=
XM_006724471.2:c.8940A>T	XP_006724534.1:p.Ala2980=
XM_006724472.2:c.8811A>T	XP_006724535.1:p.Ala2937=
XM_006724473.2:c.8802A>T	XP_006724536.1:p.Ala2934=
XM_006724474.2:c.8940A>T	XP_006724537.1:p.Ala2980=
XM_006724475.2:c.8940A>T	XP_006724538.1:p.Ala2980=
XM_011545467.1:c.8817A>T	XP_011543769.1:p.Ala2939=
XM_011545468.1:c.8940A>T	XP_011543770.1:p.Ala2980=
XM_006724469.3:c.8916A>T	XP_006724532.1:p.Ala2972=
XM_006724470.3:c.8940A>T	XP_006724533.1:p.Ala2980=
XM_006724474.3:c.8940A>T	XP_006724537.1:p.Ala2980=
XM_011545468.2:c.8940A>T	XP_011543770.1:p.Ala2980=
XM_017029328.1:c.8940A>T	XP_016884817.1:p.Ala2980=
XM_017029331.1:c.3114A>T	XP_016884820.1:p.Ala1038=
NM_000109.4:c.8916A>T	NP_000100.3:p.Ala2972=
NM_004006.3:c.8940A>T MANE Select	NP_003997.2:p.Ala2980=
NM_004011.4:c.4917A>T	NP_004002.3:p.Ala1639=
NM_004012.4:c.4908A>T	NP_004003.2:p.Ala1636=
NM_004021.3:c.1560A>T	NP_004012.2:p.Ala520=
NM_004023.3:c.1560A>T	NP_004014.2:p.Ala520=
NM_004013.3:c.1560A>T	NP_004004.2:p.Ala520=
NM_004014.3:c.753A>T	NP_004005.2:p.Ala251=
NM_004020.4:c.1560A>T	NP_004011.3:p.Ala520=
NM_004022.3:c.1560A>T	NP_004013.2:p.Ala520=