Canonical Allele Identifier: CA412665943
Gene: DMD HGNC NCBI

Linked Data

dbSNP Id: rs1603631243

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32343208G>A , CM000685.2:g.32343208G>A GRCh38
NC_000023.10:g.32361325G>A , CM000685.1:g.32361325G>A GRCh37
NC_000023.9:g.32271246G>A NCBI36
NG_012232.1:g.1001402C>T , LRG_199:g.1001402C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000358062.7:c.511C>T ENSP00000350765.3:p.Leu171Phe
ENST00000357033.9:c.5665C>T MANE Select ENSP00000354923.3:p.Leu1889Phe
ENST00000619831.5:c.1633C>T ENSP00000479270.2:p.Leu545Phe
ENST00000357033.8:c.5665C>T ENSP00000354923.3:p.Leu1889Phe
ENST00000378677.6:c.5653C>T ENSP00000367948.2:p.Leu1885Phe
ENST00000488902.5:n.336-126145C>T
ENST00000493412.1:c.322C>T ENSP00000417725.1:p.Leu108Phe
ENST00000619831.4:c.5653C>T ENSP00000479270.1:p.Leu1885Phe
ENST00000620040.4:c.5665C>T ENSP00000478150.1:p.Leu1889Phe
NM_000109.3:c.5641C>T NP_000100.2:p.Leu1881Phe
NM_004006.2:c.5665C>T , LRG_199t1:c.5665C>T NP_003997.1:p.Leu1889Phe
NM_004009.3:c.5653C>T NP_004000.1:p.Leu1885Phe
NM_004010.3:c.5296C>T NP_004001.1:p.Leu1766Phe
NM_004011.3:c.1642C>T NP_004002.2:p.Leu548Phe
NM_004012.3:c.1633C>T NP_004003.1:p.Leu545Phe
XM_006724468.2:c.5665C>T XP_006724531.1:p.Leu1889Phe
XM_006724469.2:c.5641C>T XP_006724532.1:p.Leu1881Phe
XM_006724470.2:c.5665C>T XP_006724533.1:p.Leu1889Phe
XM_006724471.2:c.5665C>T XP_006724534.1:p.Leu1889Phe
XM_006724472.2:c.5536C>T XP_006724535.1:p.Leu1846Phe
XM_006724473.2:c.5527C>T XP_006724536.1:p.Leu1843Phe
XM_006724474.2:c.5665C>T XP_006724537.1:p.Leu1889Phe
XM_006724475.2:c.5665C>T XP_006724538.1:p.Leu1889Phe
XM_011545467.1:c.5542C>T XP_011543769.1:p.Leu1848Phe
XM_011545468.1:c.5665C>T XP_011543770.1:p.Leu1889Phe
XM_011545469.1:c.5665C>T XP_011543771.1:p.Leu1889Phe
XM_006724469.3:c.5641C>T XP_006724532.1:p.Leu1881Phe
XM_006724470.3:c.5665C>T XP_006724533.1:p.Leu1889Phe
XM_006724474.3:c.5665C>T XP_006724537.1:p.Leu1889Phe
XM_011545468.2:c.5665C>T XP_011543770.1:p.Leu1889Phe
XM_017029328.1:c.5665C>T XP_016884817.1:p.Leu1889Phe
XM_017029329.1:c.5665C>T XP_016884818.1:p.Leu1889Phe
XM_017029330.2:c.5665C>T XP_016884819.1:p.Leu1889Phe
NM_000109.4:c.5641C>T NP_000100.3:p.Leu1881Phe
NM_004006.3:c.5665C>T MANE Select NP_003997.2:p.Leu1889Phe
NM_004011.4:c.1642C>T NP_004002.3:p.Leu548Phe
NM_004012.4:c.1633C>T NP_004003.2:p.Leu545Phe