Canonical Allele Identifier: CA1260160348
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71686470A= , CM000664.2:g.71686470A= GRCh38
NC_000002.11:g.71913600A= , CM000664.1:g.71913600A= GRCh37
NC_000002.10:g.71767108A= NCBI36
NG_008694.1:g.237848A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698057.1:c.3752A= ENSP00000513536.1:p.Lys1251=
ENST00000698058.1:c.2969A= ENSP00000513537.1:p.Lys990=
ENST00000698059.1:c.3077A= ENSP00000513538.1:p.Lys1026=
ENST00000258104.8:c.6221A= MANE Plus Clinical ENSP00000258104.3:p.Lys2074=
ENST00000410020.8:c.6338A= MANE Select ENSP00000386881.3:p.Lys2113=
ENST00000258104.7:c.6221A= ENSP00000258104.3:p.Lys2074=
ENST00000394120.6:c.6224A= ENSP00000377678.2:p.Lys2075=
ENST00000409366.5:c.6287A= ENSP00000386512.1:p.Lys2096=
ENST00000409582.7:c.6335A= ENSP00000386547.3:p.Lys2112=
ENST00000409651.5:c.6317A= ENSP00000386683.1:p.Lys2106=
ENST00000409744.5:c.6245A= ENSP00000386285.1:p.Lys2082=
ENST00000409762.5:c.6272A= ENSP00000387137.1:p.Lys2091=
ENST00000410020.7:c.6338A= ENSP00000386881.3:p.Lys2113=
ENST00000410041.1:c.6275A= ENSP00000386617.1:p.Lys2092=
ENST00000413539.6:c.6314A= ENSP00000407046.2:p.Lys2105=
ENST00000429174.6:c.6284A= ENSP00000398305.2:p.Lys2095=
ENST00000479049.6:n.3106A=
NM_001130455.1:c.6224A= NP_001123927.1:p.Lys2075=
NM_001130976.1:c.6179A= NP_001124448.1:p.Lys2060=
NM_001130977.1:c.6242A= NP_001124449.1:p.Lys2081=
NM_001130978.1:c.6284A= NP_001124450.1:p.Lys2095=
NM_001130979.1:c.6314A= NP_001124451.1:p.Lys2105=
NM_001130980.1:c.6272A= NP_001124452.1:p.Lys2091=
NM_001130981.1:c.6335A= NP_001124453.1:p.Lys2112=
NM_001130982.1:c.6317A= NP_001124454.1:p.Lys2106=
NM_001130983.1:c.6287A= NP_001124455.1:p.Lys2096=
NM_001130984.1:c.6245A= NP_001124456.1:p.Lys2082=
NM_001130985.1:c.6275A= NP_001124457.1:p.Lys2092=
NM_001130986.1:c.6182A= NP_001124458.1:p.Lys2061=
NM_001130987.1:c.6338A= NP_001124459.1:p.Lys2113=
NM_003494.3:c.6221A= NP_003485.1:p.Lys2074=
XM_005264584.3:c.6380A= XP_005264641.1:p.Lys2127=
XM_005264585.3:c.6377A= XP_005264642.1:p.Lys2126=
XM_005264584.4:c.6380A= XP_005264641.1:p.Lys2127=
XM_005264585.5:c.6377A= XP_005264642.1:p.Lys2126=
NM_001130987.2:c.6338A= MANE Select NP_001124459.1:p.Lys2113=
NM_001130455.2:c.6224A= NP_001123927.1:p.Lys2075=
NM_001130976.2:c.6179A= NP_001124448.1:p.Lys2060=
NM_001130977.2:c.6242A= NP_001124449.1:p.Lys2081=
NM_001130978.2:c.6284A= NP_001124450.1:p.Lys2095=
NM_001130979.2:c.6314A= NP_001124451.1:p.Lys2105=
NM_001130980.2:c.6272A= NP_001124452.1:p.Lys2091=
NM_001130981.2:c.6335A= NP_001124453.1:p.Lys2112=
NM_001130982.2:c.6317A= NP_001124454.1:p.Lys2106=
NM_001130983.2:c.6287A= NP_001124455.1:p.Lys2096=
NM_001130984.2:c.6245A= NP_001124456.1:p.Lys2082=
NM_001130985.2:c.6275A= NP_001124457.1:p.Lys2092=
NM_001130986.2:c.6182A= NP_001124458.1:p.Lys2061=
NM_003494.4:c.6221A= MANE Plus Clinical NP_003485.1:p.Lys2074=