Canonical Allele Identifier: CA1260152187
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71669128A= , CM000664.2:g.71669128A= GRCh38
NC_000002.11:g.71896258A= , CM000664.1:g.71896258A= GRCh37
NC_000002.10:g.71749766A= NCBI36
NG_008694.1:g.220506A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698057.1:c.2977A= ENSP00000513536.1:p.Ile993=
ENST00000698058.1:c.2194A= ENSP00000513537.1:p.Ile732=
ENST00000698059.1:c.2302A= ENSP00000513538.1:p.Ile768=
ENST00000258104.8:c.5446A= MANE Plus Clinical ENSP00000258104.3:p.Ile1816=
ENST00000410020.8:c.5563A= MANE Select ENSP00000386881.3:p.Ile1855=
ENST00000258104.7:c.5446A= ENSP00000258104.3:p.Ile1816=
ENST00000394120.6:c.5449A= ENSP00000377678.2:p.Ile1817=
ENST00000409366.5:c.5512A= ENSP00000386512.1:p.Ile1838=
ENST00000409582.7:c.5560A= ENSP00000386547.3:p.Ile1854=
ENST00000409651.5:c.5542A= ENSP00000386683.1:p.Ile1848=
ENST00000409744.5:c.5470A= ENSP00000386285.1:p.Ile1824=
ENST00000409762.5:c.5497A= ENSP00000387137.1:p.Ile1833=
ENST00000410020.7:c.5563A= ENSP00000386881.3:p.Ile1855=
ENST00000410041.1:c.5500A= ENSP00000386617.1:p.Ile1834=
ENST00000413539.6:c.5539A= ENSP00000407046.2:p.Ile1847=
ENST00000429174.6:c.5509A= ENSP00000398305.2:p.Ile1837=
ENST00000479049.6:n.2331A=
NM_001130455.1:c.5449A= NP_001123927.1:p.Ile1817=
NM_001130976.1:c.5404A= NP_001124448.1:p.Ile1802=
NM_001130977.1:c.5467A= NP_001124449.1:p.Ile1823=
NM_001130978.1:c.5509A= NP_001124450.1:p.Ile1837=
NM_001130979.1:c.5539A= NP_001124451.1:p.Ile1847=
NM_001130980.1:c.5497A= NP_001124452.1:p.Ile1833=
NM_001130981.1:c.5560A= NP_001124453.1:p.Ile1854=
NM_001130982.1:c.5542A= NP_001124454.1:p.Ile1848=
NM_001130983.1:c.5512A= NP_001124455.1:p.Ile1838=
NM_001130984.1:c.5470A= NP_001124456.1:p.Ile1824=
NM_001130985.1:c.5500A= NP_001124457.1:p.Ile1834=
NM_001130986.1:c.5407A= NP_001124458.1:p.Ile1803=
NM_001130987.1:c.5563A= NP_001124459.1:p.Ile1855=
NM_003494.3:c.5446A= NP_003485.1:p.Ile1816=
XM_005264584.3:c.5605A= XP_005264641.1:p.Ile1869=
XM_005264585.3:c.5602A= XP_005264642.1:p.Ile1868=
XM_005264584.4:c.5605A= XP_005264641.1:p.Ile1869=
XM_005264585.5:c.5602A= XP_005264642.1:p.Ile1868=
NM_001130987.2:c.5563A= MANE Select NP_001124459.1:p.Ile1855=
NM_001130455.2:c.5449A= NP_001123927.1:p.Ile1817=
NM_001130976.2:c.5404A= NP_001124448.1:p.Ile1802=
NM_001130977.2:c.5467A= NP_001124449.1:p.Ile1823=
NM_001130978.2:c.5509A= NP_001124450.1:p.Ile1837=
NM_001130979.2:c.5539A= NP_001124451.1:p.Ile1847=
NM_001130980.2:c.5497A= NP_001124452.1:p.Ile1833=
NM_001130981.2:c.5560A= NP_001124453.1:p.Ile1854=
NM_001130982.2:c.5542A= NP_001124454.1:p.Ile1848=
NM_001130983.2:c.5512A= NP_001124455.1:p.Ile1838=
NM_001130984.2:c.5470A= NP_001124456.1:p.Ile1824=
NM_001130985.2:c.5500A= NP_001124457.1:p.Ile1834=
NM_001130986.2:c.5407A= NP_001124458.1:p.Ile1803=
NM_003494.4:c.5446A= MANE Plus Clinical NP_003485.1:p.Ile1816=