Canonical Allele Identifier: CA2422770116
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32365073T= , CM000685.2:g.32365073T= GRCh38
NC_000023.10:g.32383190T= , CM000685.1:g.32383190T= GRCh37
NC_000023.9:g.32293111T= NCBI36
NG_012232.1:g.979537A= , LRG_199:g.979537A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357033.9:c.4972A= MANE Select ENSP00000354923.3:p.Ser1658=
ENST00000619831.5:c.940A= ENSP00000479270.2:p.Ser314=
ENST00000357033.8:c.4972A= ENSP00000354923.3:p.Ser1658=
ENST00000378677.6:c.4960A= ENSP00000367948.2:p.Ser1654=
ENST00000420596.5:c.220A= ENSP00000399897.1:p.Ser74=
ENST00000448370.5:c.94-363A= ENSP00000388559.1:n.94-363A=
ENST00000488902.5:n.336-148010A=
ENST00000619831.4:c.4960A= ENSP00000479270.1:p.Ser1654=
ENST00000620040.4:c.4972A= ENSP00000478150.1:p.Ser1658=
NM_000109.3:c.4948A= NP_000100.2:p.Ser1650=
NM_004006.2:c.4972A= , LRG_199t1:c.4972A= NP_003997.1:p.Ser1658=
NM_004009.3:c.4960A= NP_004000.1:p.Ser1654=
NM_004010.3:c.4603A= NP_004001.1:p.Ser1535=
NM_004011.3:c.949A= NP_004002.2:p.Ser317=
NM_004012.3:c.940A= NP_004003.1:p.Ser314=
XM_006724468.2:c.4972A= XP_006724531.1:p.Ser1658=
XM_006724469.2:c.4948A= XP_006724532.1:p.Ser1650=
XM_006724470.2:c.4972A= XP_006724533.1:p.Ser1658=
XM_006724471.2:c.4972A= XP_006724534.1:p.Ser1658=
XM_006724472.2:c.4843A= XP_006724535.1:p.Ser1615=
XM_006724473.2:c.4972A= XP_006724536.1:p.Ser1658=
XM_006724474.2:c.4972A= XP_006724537.1:p.Ser1658=
XM_006724475.2:c.4972A= XP_006724538.1:p.Ser1658=
XM_011545467.1:c.4972A= XP_011543769.1:p.Ser1658=
XM_011545468.1:c.4972A= XP_011543770.1:p.Ser1658=
XM_011545469.1:c.4972A= XP_011543771.1:p.Ser1658=
XM_006724469.3:c.4948A= XP_006724532.1:p.Ser1650=
XM_006724470.3:c.4972A= XP_006724533.1:p.Ser1658=
XM_006724474.3:c.4972A= XP_006724537.1:p.Ser1658=
XM_011545468.2:c.4972A= XP_011543770.1:p.Ser1658=
XM_017029328.1:c.4972A= XP_016884817.1:p.Ser1658=
XM_017029329.1:c.4972A= XP_016884818.1:p.Ser1658=
XM_017029330.2:c.4972A= XP_016884819.1:p.Ser1658=
NM_000109.4:c.4948A= NP_000100.3:p.Ser1650=
NM_004006.3:c.4972A= MANE Select NP_003997.2:p.Ser1658=
NM_004011.4:c.949A= NP_004002.3:p.Ser317=
NM_004012.4:c.940A= NP_004003.2:p.Ser314=