Canonical Allele Identifier: CA1260152182
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71669122C= , CM000664.2:g.71669122C= GRCh38
NC_000002.11:g.71896252C= , CM000664.1:g.71896252C= GRCh37
NC_000002.10:g.71749760C= NCBI36
NG_008694.1:g.220500C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698057.1:c.2971C= ENSP00000513536.1:p.Arg991=
ENST00000698058.1:c.2188C= ENSP00000513537.1:p.Arg730=
ENST00000698059.1:c.2296C= ENSP00000513538.1:p.Arg766=
ENST00000258104.8:c.5440C= MANE Plus Clinical ENSP00000258104.3:p.Arg1814=
ENST00000410020.8:c.5557C= MANE Select ENSP00000386881.3:p.Arg1853=
ENST00000258104.7:c.5440C= ENSP00000258104.3:p.Arg1814=
ENST00000394120.6:c.5443C= ENSP00000377678.2:p.Arg1815=
ENST00000409366.5:c.5506C= ENSP00000386512.1:p.Arg1836=
ENST00000409582.7:c.5554C= ENSP00000386547.3:p.Arg1852=
ENST00000409651.5:c.5536C= ENSP00000386683.1:p.Arg1846=
ENST00000409744.5:c.5464C= ENSP00000386285.1:p.Arg1822=
ENST00000409762.5:c.5491C= ENSP00000387137.1:p.Arg1831=
ENST00000410020.7:c.5557C= ENSP00000386881.3:p.Arg1853=
ENST00000410041.1:c.5494C= ENSP00000386617.1:p.Arg1832=
ENST00000413539.6:c.5533C= ENSP00000407046.2:p.Arg1845=
ENST00000429174.6:c.5503C= ENSP00000398305.2:p.Arg1835=
ENST00000479049.6:n.2325C=
NM_001130455.1:c.5443C= NP_001123927.1:p.Arg1815=
NM_001130976.1:c.5398C= NP_001124448.1:p.Arg1800=
NM_001130977.1:c.5461C= NP_001124449.1:p.Arg1821=
NM_001130978.1:c.5503C= NP_001124450.1:p.Arg1835=
NM_001130979.1:c.5533C= NP_001124451.1:p.Arg1845=
NM_001130980.1:c.5491C= NP_001124452.1:p.Arg1831=
NM_001130981.1:c.5554C= NP_001124453.1:p.Arg1852=
NM_001130982.1:c.5536C= NP_001124454.1:p.Arg1846=
NM_001130983.1:c.5506C= NP_001124455.1:p.Arg1836=
NM_001130984.1:c.5464C= NP_001124456.1:p.Arg1822=
NM_001130985.1:c.5494C= NP_001124457.1:p.Arg1832=
NM_001130986.1:c.5401C= NP_001124458.1:p.Arg1801=
NM_001130987.1:c.5557C= NP_001124459.1:p.Arg1853=
NM_003494.3:c.5440C= NP_003485.1:p.Arg1814=
XM_005264584.3:c.5599C= XP_005264641.1:p.Arg1867=
XM_005264585.3:c.5596C= XP_005264642.1:p.Arg1866=
XM_005264584.4:c.5599C= XP_005264641.1:p.Arg1867=
XM_005264585.5:c.5596C= XP_005264642.1:p.Arg1866=
NM_001130987.2:c.5557C= MANE Select NP_001124459.1:p.Arg1853=
NM_001130455.2:c.5443C= NP_001123927.1:p.Arg1815=
NM_001130976.2:c.5398C= NP_001124448.1:p.Arg1800=
NM_001130977.2:c.5461C= NP_001124449.1:p.Arg1821=
NM_001130978.2:c.5503C= NP_001124450.1:p.Arg1835=
NM_001130979.2:c.5533C= NP_001124451.1:p.Arg1845=
NM_001130980.2:c.5491C= NP_001124452.1:p.Arg1831=
NM_001130981.2:c.5554C= NP_001124453.1:p.Arg1852=
NM_001130982.2:c.5536C= NP_001124454.1:p.Arg1846=
NM_001130983.2:c.5506C= NP_001124455.1:p.Arg1836=
NM_001130984.2:c.5464C= NP_001124456.1:p.Arg1822=
NM_001130985.2:c.5494C= NP_001124457.1:p.Arg1832=
NM_001130986.2:c.5401C= NP_001124458.1:p.Arg1801=
NM_003494.4:c.5440C= MANE Plus Clinical NP_003485.1:p.Arg1814=