Canonical Allele Identifier: CA2693396391
Gene: DMD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32464500dup , CM000685.2:g.32464500dup GRCh38
NC_000023.10:g.32482617dup , CM000685.1:g.32482617dup GRCh37
NC_000023.9:g.32392538dup NCBI36
NG_012232.1:g.880113dup , LRG_199:g.880113dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682899.1:n.3483+89dup
ENST00000357033.9:c.3276+89dup MANE Select ENSP00000354923.3:n.3276+89dup
ENST00000357033.8:c.3276+89dup ENSP00000354923.3:n.3276+89dup
ENST00000378677.6:c.3264+89dup ENSP00000367948.2:n.3264+89dup
ENST00000420596.5:c.94-99298dup ENSP00000399897.1:n.94-99298dup
ENST00000448370.5:c.94-99787dup ENSP00000388559.1:n.94-99787dup
ENST00000488902.5:n.336-247434dup
ENST00000619831.4:c.3264+89dup ENSP00000479270.1:n.3264+89dup
ENST00000620040.4:c.3276+89dup ENSP00000478150.1:n.3276+89dup
NM_000109.3:c.3252+89dup NP_000100.2:n.3252+89dup
NM_004006.2:c.3276+89dup , LRG_199t1:c.3276+89dup NP_003997.1:n.3276+89dup
NM_004009.3:c.3264+89dup NP_004000.1:n.3264+89dup
NM_004010.3:c.2907+89dup NP_004001.1:n.2907+89dup
XM_006724468.2:c.3276+89dup XP_006724531.1:n.3276+89dup
XM_006724469.2:c.3252+89dup XP_006724532.1:n.3252+89dup
XM_006724470.2:c.3276+89dup XP_006724533.1:n.3276+89dup
XM_006724471.2:c.3276+89dup XP_006724534.1:n.3276+89dup
XM_006724472.2:c.3147+89dup XP_006724535.1:n.3147+89dup
XM_006724473.2:c.3276+89dup XP_006724536.1:n.3276+89dup
XM_006724474.2:c.3276+89dup XP_006724537.1:n.3276+89dup
XM_006724475.2:c.3276+89dup XP_006724538.1:n.3276+89dup
XM_011545467.1:c.3276+89dup XP_011543769.1:n.3276+89dup
XM_011545468.1:c.3276+89dup XP_011543770.1:n.3276+89dup
XM_011545469.1:c.3276+89dup XP_011543771.1:n.3276+89dup
XM_006724469.3:c.3252+89dup XP_006724532.1:n.3252+89dup
XM_006724470.3:c.3276+89dup XP_006724533.1:n.3276+89dup
XM_006724474.3:c.3276+89dup XP_006724537.1:n.3276+89dup
XM_011545468.2:c.3276+89dup XP_011543770.1:n.3276+89dup
XM_017029328.1:c.3276+89dup XP_016884817.1:n.3276+89dup
XM_017029329.1:c.3276+89dup XP_016884818.1:n.3276+89dup
XM_017029330.2:c.3276+89dup XP_016884819.1:n.3276+89dup
NM_000109.4:c.3252+89dup NP_000100.3:n.3252+89dup
NM_004006.3:c.3276+89dup MANE Select NP_003997.2:n.3276+89dup