Canonical Allele Identifier: CA1260160342
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71686458A= , CM000664.2:g.71686458A= GRCh38
NC_000002.11:g.71913588A= , CM000664.1:g.71913588A= GRCh37
NC_000002.10:g.71767096A= NCBI36
NG_008694.1:g.237836A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698057.1:c.3740A= ENSP00000513536.1:p.Tyr1247=
ENST00000698058.1:c.2957A= ENSP00000513537.1:p.Tyr986=
ENST00000698059.1:c.3065A= ENSP00000513538.1:p.Tyr1022=
ENST00000258104.8:c.6209A= MANE Plus Clinical ENSP00000258104.3:p.Tyr2070=
ENST00000410020.8:c.6326A= MANE Select ENSP00000386881.3:p.Tyr2109=
ENST00000258104.7:c.6209A= ENSP00000258104.3:p.Tyr2070=
ENST00000394120.6:c.6212A= ENSP00000377678.2:p.Tyr2071=
ENST00000409366.5:c.6275A= ENSP00000386512.1:p.Tyr2092=
ENST00000409582.7:c.6323A= ENSP00000386547.3:p.Tyr2108=
ENST00000409651.5:c.6305A= ENSP00000386683.1:p.Tyr2102=
ENST00000409744.5:c.6233A= ENSP00000386285.1:p.Tyr2078=
ENST00000409762.5:c.6260A= ENSP00000387137.1:p.Tyr2087=
ENST00000410020.7:c.6326A= ENSP00000386881.3:p.Tyr2109=
ENST00000410041.1:c.6263A= ENSP00000386617.1:p.Tyr2088=
ENST00000413539.6:c.6302A= ENSP00000407046.2:p.Tyr2101=
ENST00000429174.6:c.6272A= ENSP00000398305.2:p.Tyr2091=
ENST00000479049.6:n.3094A=
NM_001130455.1:c.6212A= NP_001123927.1:p.Tyr2071=
NM_001130976.1:c.6167A= NP_001124448.1:p.Tyr2056=
NM_001130977.1:c.6230A= NP_001124449.1:p.Tyr2077=
NM_001130978.1:c.6272A= NP_001124450.1:p.Tyr2091=
NM_001130979.1:c.6302A= NP_001124451.1:p.Tyr2101=
NM_001130980.1:c.6260A= NP_001124452.1:p.Tyr2087=
NM_001130981.1:c.6323A= NP_001124453.1:p.Tyr2108=
NM_001130982.1:c.6305A= NP_001124454.1:p.Tyr2102=
NM_001130983.1:c.6275A= NP_001124455.1:p.Tyr2092=
NM_001130984.1:c.6233A= NP_001124456.1:p.Tyr2078=
NM_001130985.1:c.6263A= NP_001124457.1:p.Tyr2088=
NM_001130986.1:c.6170A= NP_001124458.1:p.Tyr2057=
NM_001130987.1:c.6326A= NP_001124459.1:p.Tyr2109=
NM_003494.3:c.6209A= NP_003485.1:p.Tyr2070=
XM_005264584.3:c.6368A= XP_005264641.1:p.Tyr2123=
XM_005264585.3:c.6365A= XP_005264642.1:p.Tyr2122=
XM_005264584.4:c.6368A= XP_005264641.1:p.Tyr2123=
XM_005264585.5:c.6365A= XP_005264642.1:p.Tyr2122=
NM_001130987.2:c.6326A= MANE Select NP_001124459.1:p.Tyr2109=
NM_001130455.2:c.6212A= NP_001123927.1:p.Tyr2071=
NM_001130976.2:c.6167A= NP_001124448.1:p.Tyr2056=
NM_001130977.2:c.6230A= NP_001124449.1:p.Tyr2077=
NM_001130978.2:c.6272A= NP_001124450.1:p.Tyr2091=
NM_001130979.2:c.6302A= NP_001124451.1:p.Tyr2101=
NM_001130980.2:c.6260A= NP_001124452.1:p.Tyr2087=
NM_001130981.2:c.6323A= NP_001124453.1:p.Tyr2108=
NM_001130982.2:c.6305A= NP_001124454.1:p.Tyr2102=
NM_001130983.2:c.6275A= NP_001124455.1:p.Tyr2092=
NM_001130984.2:c.6233A= NP_001124456.1:p.Tyr2078=
NM_001130985.2:c.6263A= NP_001124457.1:p.Tyr2088=
NM_001130986.2:c.6170A= NP_001124458.1:p.Tyr2057=
NM_003494.4:c.6209A= MANE Plus Clinical NP_003485.1:p.Tyr2070=