Canonical Allele Identifier: CA2422815754
Gene: DMD HGNC NCBI

Linked Data

dbSNP Id: rs2098394581

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32464487_32464490dup , CM000685.2:g.32464487_32464490dup GRCh38
NC_000023.10:g.32482604_32482607dup , CM000685.1:g.32482604_32482607dup GRCh37
NC_000023.9:g.32392525_32392528dup NCBI36
NG_012232.1:g.880121_880124dup , LRG_199:g.880121_880124dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682899.1:n.3483+97_3483+100dup
ENST00000357033.9:c.3276+97_3276+100dup MANE Select ENSP00000354923.3:n.3276+97_3276+100dup
ENST00000357033.8:c.3276+97_3276+100dup ENSP00000354923.3:n.3276+97_3276+100dup
ENST00000378677.6:c.3264+97_3264+100dup ENSP00000367948.2:n.3264+97_3264+100dup
ENST00000420596.5:c.94-99290_94-99287dup ENSP00000399897.1:n.94-99290_94-99287dup
ENST00000448370.5:c.94-99779_94-99776dup ENSP00000388559.1:n.94-99779_94-99776dup
ENST00000488902.5:n.336-247426_336-247423dup
ENST00000619831.4:c.3264+97_3264+100dup ENSP00000479270.1:n.3264+97_3264+100dup
ENST00000620040.4:c.3276+97_3276+100dup ENSP00000478150.1:n.3276+97_3276+100dup
NM_000109.3:c.3252+97_3252+100dup NP_000100.2:n.3252+97_3252+100dup
NM_004006.2:c.3276+97_3276+100dup , LRG_199t1:c.3276+97_3276+100dup NP_003997.1:n.3276+97_3276+100dup
NM_004009.3:c.3264+97_3264+100dup NP_004000.1:n.3264+97_3264+100dup
NM_004010.3:c.2907+97_2907+100dup NP_004001.1:n.2907+97_2907+100dup
XM_006724468.2:c.3276+97_3276+100dup XP_006724531.1:n.3276+97_3276+100dup
XM_006724469.2:c.3252+97_3252+100dup XP_006724532.1:n.3252+97_3252+100dup
XM_006724470.2:c.3276+97_3276+100dup XP_006724533.1:n.3276+97_3276+100dup
XM_006724471.2:c.3276+97_3276+100dup XP_006724534.1:n.3276+97_3276+100dup
XM_006724472.2:c.3147+97_3147+100dup XP_006724535.1:n.3147+97_3147+100dup
XM_006724473.2:c.3276+97_3276+100dup XP_006724536.1:n.3276+97_3276+100dup
XM_006724474.2:c.3276+97_3276+100dup XP_006724537.1:n.3276+97_3276+100dup
XM_006724475.2:c.3276+97_3276+100dup XP_006724538.1:n.3276+97_3276+100dup
XM_011545467.1:c.3276+97_3276+100dup XP_011543769.1:n.3276+97_3276+100dup
XM_011545468.1:c.3276+97_3276+100dup XP_011543770.1:n.3276+97_3276+100dup
XM_011545469.1:c.3276+97_3276+100dup XP_011543771.1:n.3276+97_3276+100dup
XM_006724469.3:c.3252+97_3252+100dup XP_006724532.1:n.3252+97_3252+100dup
XM_006724470.3:c.3276+97_3276+100dup XP_006724533.1:n.3276+97_3276+100dup
XM_006724474.3:c.3276+97_3276+100dup XP_006724537.1:n.3276+97_3276+100dup
XM_011545468.2:c.3276+97_3276+100dup XP_011543770.1:n.3276+97_3276+100dup
XM_017029328.1:c.3276+97_3276+100dup XP_016884817.1:n.3276+97_3276+100dup
XM_017029329.1:c.3276+97_3276+100dup XP_016884818.1:n.3276+97_3276+100dup
XM_017029330.2:c.3276+97_3276+100dup XP_016884819.1:n.3276+97_3276+100dup
NM_000109.4:c.3252+97_3252+100dup NP_000100.3:n.3252+97_3252+100dup
NM_004006.3:c.3276+97_3276+100dup MANE Select NP_003997.2:n.3276+97_3276+100dup