Canonical Allele Identifier: CA1260156891
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71679210A= , CM000664.2:g.71679210A= GRCh38
NC_000002.11:g.71906340A= , CM000664.1:g.71906340A= GRCh37
NC_000002.10:g.71759848A= NCBI36
NG_008694.1:g.230588A=

Transcript Alleles

HGVS Amino-acid change
ENST00000698057.1:c.3452A= ENSP00000513536.1:p.Glu1151=
ENST00000698058.1:c.2669A= ENSP00000513537.1:p.Glu890=
ENST00000698059.1:c.2777A= ENSP00000513538.1:p.Glu926=
ENST00000258104.8:c.5921A= MANE Plus Clinical ENSP00000258104.3:p.Glu1974=
ENST00000410020.8:c.6038A= MANE Select ENSP00000386881.3:p.Glu2013=
ENST00000258104.7:c.5921A= ENSP00000258104.3:p.Glu1974=
ENST00000394120.6:c.5924A= ENSP00000377678.2:p.Glu1975=
ENST00000409366.5:c.5987A= ENSP00000386512.1:p.Glu1996=
ENST00000409582.7:c.6035A= ENSP00000386547.3:p.Glu2012=
ENST00000409651.5:c.6017A= ENSP00000386683.1:p.Glu2006=
ENST00000409744.5:c.5945A= ENSP00000386285.1:p.Glu1982=
ENST00000409762.5:c.5972A= ENSP00000387137.1:p.Glu1991=
ENST00000410020.7:c.6038A= ENSP00000386881.3:p.Glu2013=
ENST00000410041.1:c.5975A= ENSP00000386617.1:p.Glu1992=
ENST00000413539.6:c.6014A= ENSP00000407046.2:p.Glu2005=
ENST00000429174.6:c.5984A= ENSP00000398305.2:p.Glu1995=
ENST00000479049.6:n.2806A=
NM_001130455.1:c.5924A= NP_001123927.1:p.Glu1975=
NM_001130976.1:c.5879A= NP_001124448.1:p.Glu1960=
NM_001130977.1:c.5942A= NP_001124449.1:p.Glu1981=
NM_001130978.1:c.5984A= NP_001124450.1:p.Glu1995=
NM_001130979.1:c.6014A= NP_001124451.1:p.Glu2005=
NM_001130980.1:c.5972A= NP_001124452.1:p.Glu1991=
NM_001130981.1:c.6035A= NP_001124453.1:p.Glu2012=
NM_001130982.1:c.6017A= NP_001124454.1:p.Glu2006=
NM_001130983.1:c.5987A= NP_001124455.1:p.Glu1996=
NM_001130984.1:c.5945A= NP_001124456.1:p.Glu1982=
NM_001130985.1:c.5975A= NP_001124457.1:p.Glu1992=
NM_001130986.1:c.5882A= NP_001124458.1:p.Glu1961=
NM_001130987.1:c.6038A= NP_001124459.1:p.Glu2013=
NM_003494.3:c.5921A= NP_003485.1:p.Glu1974=
XM_005264584.3:c.6080A= XP_005264641.1:p.Glu2027=
XM_005264585.3:c.6077A= XP_005264642.1:p.Glu2026=
XM_005264584.4:c.6080A= XP_005264641.1:p.Glu2027=
XM_005264585.5:c.6077A= XP_005264642.1:p.Glu2026=
NM_001130987.2:c.6038A= MANE Select NP_001124459.1:p.Glu2013=
NM_001130455.2:c.5924A= NP_001123927.1:p.Glu1975=
NM_001130976.2:c.5879A= NP_001124448.1:p.Glu1960=
NM_001130977.2:c.5942A= NP_001124449.1:p.Glu1981=
NM_001130978.2:c.5984A= NP_001124450.1:p.Glu1995=
NM_001130979.2:c.6014A= NP_001124451.1:p.Glu2005=
NM_001130980.2:c.5972A= NP_001124452.1:p.Glu1991=
NM_001130981.2:c.6035A= NP_001124453.1:p.Glu2012=
NM_001130982.2:c.6017A= NP_001124454.1:p.Glu2006=
NM_001130983.2:c.5987A= NP_001124455.1:p.Glu1996=
NM_001130984.2:c.5945A= NP_001124456.1:p.Glu1982=
NM_001130985.2:c.5975A= NP_001124457.1:p.Glu1992=
NM_001130986.2:c.5882A= NP_001124458.1:p.Glu1961=
NM_003494.4:c.5921A= MANE Plus Clinical NP_003485.1:p.Glu1974=