Canonical Allele Identifier: CA2422811191
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32454680T= , CM000685.2:g.32454680T= GRCh38
NC_000023.10:g.32472797T= , CM000685.1:g.32472797T= GRCh37
NC_000023.9:g.32382718T= NCBI36
NG_012232.1:g.889930A= , LRG_199:g.889930A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682899.1:n.3792A=
ENST00000357033.9:c.3585A= MANE Select ENSP00000354923.3:p.Lys1195=
ENST00000357033.8:c.3585A= ENSP00000354923.3:p.Lys1195=
ENST00000378677.6:c.3573A= ENSP00000367948.2:p.Lys1191=
ENST00000420596.5:c.94-89481A= ENSP00000399897.1:n.94-89481A=
ENST00000448370.5:c.94-89970A= ENSP00000388559.1:n.94-89970A=
ENST00000488902.5:n.336-237617A=
ENST00000619831.4:c.3573A= ENSP00000479270.1:p.Lys1191=
ENST00000620040.4:c.3585A= ENSP00000478150.1:p.Lys1195=
NM_000109.3:c.3561A= NP_000100.2:p.Lys1187=
NM_004006.2:c.3585A= , LRG_199t1:c.3585A= NP_003997.1:p.Lys1195=
NM_004009.3:c.3573A= NP_004000.1:p.Lys1191=
NM_004010.3:c.3216A= NP_004001.1:p.Lys1072=
XM_006724468.2:c.3585A= XP_006724531.1:p.Lys1195=
XM_006724469.2:c.3561A= XP_006724532.1:p.Lys1187=
XM_006724470.2:c.3585A= XP_006724533.1:p.Lys1195=
XM_006724471.2:c.3585A= XP_006724534.1:p.Lys1195=
XM_006724472.2:c.3456A= XP_006724535.1:p.Lys1152=
XM_006724473.2:c.3585A= XP_006724536.1:p.Lys1195=
XM_006724474.2:c.3585A= XP_006724537.1:p.Lys1195=
XM_006724475.2:c.3585A= XP_006724538.1:p.Lys1195=
XM_011545467.1:c.3585A= XP_011543769.1:p.Lys1195=
XM_011545468.1:c.3585A= XP_011543770.1:p.Lys1195=
XM_011545469.1:c.3585A= XP_011543771.1:p.Lys1195=
XM_006724469.3:c.3561A= XP_006724532.1:p.Lys1187=
XM_006724470.3:c.3585A= XP_006724533.1:p.Lys1195=
XM_006724474.3:c.3585A= XP_006724537.1:p.Lys1195=
XM_011545468.2:c.3585A= XP_011543770.1:p.Lys1195=
XM_017029328.1:c.3585A= XP_016884817.1:p.Lys1195=
XM_017029329.1:c.3585A= XP_016884818.1:p.Lys1195=
XM_017029330.2:c.3585A= XP_016884819.1:p.Lys1195=
NM_000109.4:c.3561A= NP_000100.3:p.Lys1187=
NM_004006.3:c.3585A= MANE Select NP_003997.2:p.Lys1195=