Canonical Allele Identifier: CA10377934
Gene: DMD HGNC NCBI

Linked Data

dbSNP Id: rs772879530

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.31444528_31444542dup , CM000685.2:g.31444528_31444542dup GRCh38
NC_000023.10:g.31462645_31462659dup , CM000685.1:g.31462645_31462659dup GRCh37
NC_000023.9:g.31372566_31372580dup NCBI36
NG_012232.1:g.1900069_1900083dup , LRG_199:g.1900069_1900083dup

Transcript Alleles

HGVS Amino-acid change
ENST00000358062.7:c.3870_3884dup ENSP00000350765.3:p.Tyr1294_Asn1295insLys...
ENST00000682238.1:c.1644_1658dup ENSP00000508124.1:p.Tyr552_Asn553insLysLe...
ENST00000683450.1:n.2489_2503dup
ENST00000683957.1:n.2516_2530dup
ENST00000684130.1:c.1644_1658dup ENSP00000508037.1:p.Tyr552_Asn553insLysLe...
ENST00000343523.7:c.879_893dup ENSP00000340057.4:p.Tyr297_Asn298insLysLe...
ENST00000357033.9:c.9024_9038dup MANE Select ENSP00000354923.3:p.Tyr3012_Asn3013insLys...
ENST00000619831.5:c.4992_5006dup ENSP00000479270.2:p.Tyr1668_Asn1669insLys...
ENST00000620040.5:c.1644_1658dup ENSP00000478150.2:p.Tyr552_Asn553insLysLe...
ENST00000680961.1:c.1644_1658dup ENSP00000506386.1:p.Tyr552_Asn553insLysLe...
ENST00000681646.1:n.2685_2699dup
ENST00000343523.6:c.837_851dup ENSP00000340057.3:p.Tyr283_Asn284insLysLe...
ENST00000357033.8:c.9024_9038dup ENSP00000354923.3:p.Tyr3012_Asn3013insLys...
ENST00000358062.6:c.2112_2126dup ENSP00000350765.2:p.Tyr708_Asn709insLysLe...
ENST00000359836.5:c.1644_1658dup ENSP00000352894.1:p.Tyr552_Asn553insLysLe...
ENST00000378677.6:c.9012_9026dup ENSP00000367948.2:p.Tyr3008_Asn3009insLys...
ENST00000378707.7:c.1644_1658dup ENSP00000367979.3:p.Tyr552_Asn553insLysLe...
ENST00000474231.5:c.1644_1658dup ENSP00000417123.1:p.Tyr552_Asn553insLysLe...
ENST00000541735.5:c.1644_1658dup ENSP00000444119.1:p.Tyr552_Asn553insLysLe...
ENST00000619831.4:c.9009_9023dup ENSP00000479270.1:p.Tyr3007_Asn3008insLys...
ENST00000620040.4:c.9021_9035dup ENSP00000478150.1:p.Tyr3011_Asn3012insLys...
NM_000109.3:c.9000_9014dup NP_000100.2:p.Tyr3004_Asn3005insLysLeuSer...
NM_004006.2:c.9024_9038dup , LRG_199t1:c.9024_9038dup NP_003997.1:p.Tyr3012_Asn3013insLysLeuSer...
NM_004009.3:c.9012_9026dup NP_004000.1:p.Tyr3008_Asn3009insLysLeuSer...
NM_004010.3:c.8655_8669dup NP_004001.1:p.Tyr2889_Asn2890insLysLeuSer...
NM_004011.3:c.5001_5015dup NP_004002.2:p.Tyr1671_Asn1672insLysLeuSer...
NM_004012.3:c.4992_5006dup NP_004003.1:p.Tyr1668_Asn1669insLysLeuSer...
NM_004013.2:c.1644_1658dup NP_004004.1:p.Tyr552_Asn553insLysLeuSerPr...
NM_004014.2:c.837_851dup NP_004005.1:p.Tyr283_Asn284insLysLeuSerPr...
NM_004020.3:c.1644_1658dup NP_004011.2:p.Tyr552_Asn553insLysLeuSerPr...
NM_004021.2:c.1644_1658dup NP_004012.1:p.Tyr552_Asn553insLysLeuSerPr...
NM_004022.2:c.1644_1658dup NP_004013.1:p.Tyr552_Asn553insLysLeuSerPr...
NM_004023.2:c.1644_1658dup NP_004014.1:p.Tyr552_Asn553insLysLeuSerPr...
XM_006724468.2:c.9024_9038dup XP_006724531.1:p.Tyr3012_Asn3013insLysLeu...
XM_006724469.2:c.9000_9014dup XP_006724532.1:p.Tyr3004_Asn3005insLysLeu...
XM_006724470.2:c.9024_9038dup XP_006724533.1:p.Tyr3012_Asn3013insLysLeu...
XM_006724471.2:c.9024_9038dup XP_006724534.1:p.Tyr3012_Asn3013insLysLeu...
XM_006724472.2:c.8895_8909dup XP_006724535.1:p.Tyr2969_Asn2970insLysLeu...
XM_006724473.2:c.8886_8900dup XP_006724536.1:p.Tyr2966_Asn2967insLysLeu...
XM_006724474.2:c.9024_9038dup XP_006724537.1:p.Tyr3012_Asn3013insLysLeu...
XM_006724475.2:c.9024_9038dup XP_006724538.1:p.Tyr3012_Asn3013insLysLeu...
XM_011545467.1:c.8901_8915dup XP_011543769.1:p.Tyr2971_Asn2972insLysLeu...
XM_011545468.1:c.9024_9038dup XP_011543770.1:p.Tyr3012_Asn3013insLysLeu...
XM_006724469.3:c.9000_9014dup XP_006724532.1:p.Tyr3004_Asn3005insLysLeu...
XM_006724470.3:c.9024_9038dup XP_006724533.1:p.Tyr3012_Asn3013insLysLeu...
XM_006724474.3:c.9024_9038dup XP_006724537.1:p.Tyr3012_Asn3013insLysLeu...
XM_011545468.2:c.9024_9038dup XP_011543770.1:p.Tyr3012_Asn3013insLysLeu...
XM_017029328.1:c.9024_9038dup XP_016884817.1:p.Tyr3012_Asn3013insLysLeu...
XM_017029331.1:c.3198_3212dup XP_016884820.1:p.Tyr1070_Asn1071insLysLeu...
NM_000109.4:c.9000_9014dup NP_000100.3:p.Tyr3004_Asn3005insLysLeuSer...
NM_004006.3:c.9024_9038dup MANE Select NP_003997.2:p.Tyr3012_Asn3013insLysLeuSer...
NM_004011.4:c.5001_5015dup NP_004002.3:p.Tyr1671_Asn1672insLysLeuSer...
NM_004012.4:c.4992_5006dup NP_004003.2:p.Tyr1668_Asn1669insLysLeuSer...
NM_004021.3:c.1644_1658dup NP_004012.2:p.Tyr552_Asn553insLysLeuSerPr...
NM_004023.3:c.1644_1658dup NP_004014.2:p.Tyr552_Asn553insLysLeuSerPr...
NM_004013.3:c.1644_1658dup NP_004004.2:p.Tyr552_Asn553insLysLeuSerPr...
NM_004014.3:c.837_851dup NP_004005.2:p.Tyr283_Asn284insLysLeuSerPr...
NM_004020.4:c.1644_1658dup NP_004011.3:p.Tyr552_Asn553insLysLeuSerPr...
NM_004022.3:c.1644_1658dup NP_004013.2:p.Tyr552_Asn553insLysLeuSerPr...